m+Medelevator.RU
← Поиск публикаций
CA: a cancer journal for clinicians · 2024

Geriatric assessment for the practicing clinician: The why, what, and how.

Название и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Magnuson A, Loh KP, Stauffer F, Dale W, Gilmore N, Kadambi S, Klepin HD, Kyi K, Lowenstein LM, Phillips T, Ramsdale E, Schiaffino MK, Simmons JF, Williams GR, Zittel J, Mohile S

Аннотация

Older adults with cancer heterogeneously experience health care, treatment, and symptoms. Geriatric assessment (GA) offers a comprehensive evaluation of an older individual's health status and can predict cancer-related outcomes in individuals with solid tumors and those with hematologic malignancies. In the last decade, randomized controlled trials have demonstrated the benefits of GA and GA management (GAM), which uses GA information to provide tailored intervention strategies to address GA impairments (e.g., implementing physical therapy for impaired physical function). Multiple phase 3 clinical trials in older adults with solid tumors and hematologic malignancies have demonstrated that GAM improves treatment completion, quality of life, communication, and advance care planning while reducing treatment-related toxicity, falls, and polypharmacy. Nonetheless, implementation and uptake of GAM remain challenging. Various strategies have been proposed, including the use of GA screening tools, to identify patients most likely to benefit from GAM, the systematic engagement of the oncology workforce in the delivery of GAM, and the integration of technologies like telemedicine and mobile health to enhance the availability of GA and GAM interventions. Health inequities in minoritized groups persist, and systematic GA implementation has the potential to capture social determinants of health that are relevant to equitable care. Caregivers play an important role in cancer care and experience burden themselves. GA can guide dyadic supportive care interventions, ultimately helping both patients and caregivers achieve optimal health.

Перевод полного текста: Перевод в очереди

Читать найденный полный текст

https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

INTRODUCTION

In an aging global population, the intersection of oncology and geriatrics becomes increasingly important. Older adults with cancer present a complicated set of medical, social, economic, and physical circumstances, necessitating personalized approaches. The aging process is a heterogeneous experience, and chronologic age alone has proven an unreliable surrogate for functional and health status for older adults, particularly those with cancer considering treatment.

Traditionally, oncology studies have incorporated brief measures of functional health status, most commonly the Eastern Cooperative Oncology Group performance status (ECOG PS) 1 or the Karnofsky performance scale. 2 Reliance on these conventional measures of function, however, does not provide a nuanced picture of an older adult’s overall health status, which can lead to an unreliable prediction of how a patient will tolerate cancer therapy. 3 These performance scales consist of a user‐dependent numeric estimation of physical function and are subject to both bias and variability based on the observer. 4 , 5 Although a poor ECOG PS correlates well with abnormalities in physical function, it correlates only moderately well with impaired physical performance, cognition, and psychological assessments; and it does not reflect other domains, including nutritional status, social environment, and comorbidities. 4 , 6 Biases have been observed in physician assessments of performance status, whereby older adults are assigned worse scores than younger counterparts despite equivalent physical capacities. 7 Accurate assessment of health status is critical for clinical decision making for cancer treatment and for eligibility for clinical trials; a more comprehensive assessment of health status is clearly needed. 8

Geriatric assessment (GA) utilizes measures that evaluate clinically relevant domains in older adults, including physical performance, functional status, comorbidity, polypharmacy, nutrition, cognition, social support, and psychological status. 9 , 10 In older adults with cancer, integration of GA into oncology care is now guideline‐recommended to inform decision making and improve outcomes. In 2014, the International Society of Geriatric Oncology (SIOG) advocated a standardized assessment of geriatric domains, such as function, comorbidity, social support, nutrition, and geriatric syndromes (i.e., clinical syndromes that increase the risk of adverse outcomes in older adults) 11 ; at that time, however, the expert SIOG panel could not recommend specific tools due to insufficient evidence. Over the last 10 years, SIOG has summarized the evidence for GA in treatment decision making for many solid tumor malignancies, including breast cancer, 12 bladder cancer, 13 and renal cell carcinoma. 14 More recently, SIOG has recommended the integration of GA into the care of older adults with hematologic malignancies, including acute myelogenous leukemia, 15 acute promyelocytic leukemia, 16 and chronic lymphocytic leukemia. 17 The American Society of Clinical Oncology (ASCO) 18 and the National Comprehensive Cancer Network 19 have concluded that GA measures could predict adverse outcomes from cancer therapy in older adults and thus have recommended their use for treatment decision making. In 2023, 10 An ASCO expert panel summarized data from randomized controlled studies demonstrating the benefits of GA and GA management (GAM) for older patients with cancer; in GAM care‐delivery models, GA guides therapeutic decision making and evidence‐based, aging‐sensitive management interventions to address geriatric impairments (e.g., physical therapy for an older adult who is falling). The ASCO panel proposed the adoption of a practical GA (PGA) designed to guide management and overcome barriers to implementation in clinical practice, including low‐resource settings. 20

Herein, we summarize the evidence supporting the utility of GA in the prediction of treatment‐related toxicity and data supporting GAM care‐delivery models to improve communication, reduce treatment‐related toxicity, and enhance quality of life. We also provide evidence for the feasibility of integrating GA into oncology care, the utility of screening tools as a mechanism to identify older patients with cancer who would benefit from GA, and practical suggestions to overcome barriers to the implementation of a GAM care‐delivery model. Furthermore, we discuss recommendations for future work to optimize GA for diverse populations and dyadic GAM interventions for patients and caregivers. The goal of this review is to stress the ways that GAM can help their older patients and their caregivers challenged by cancer and provide the information needed to champion this important care‐delivery model in their practices.

GA PREDICTIVE MODELS FOR TREATMENT‐RELATED TOXICITY IN OLDER ADULTS WITH CANCER

Several predictive models based on GA domains have been created to guide management for older adults with cancer ( Table 1 ). The Cancer and Aging Research Group (CARG) model was developed and subsequently validated by Hurria et al. 21 to predict the risk of severe chemotherapy toxicity (i.e., clinician‐rated grade 3–5 adverse events according to the Common Terminology Criteria for Adverse Events). Using core clinical variables (e.g., age, renal function, tumor and treatment characteristics) and GA measures (e.g., fall history, social activities, hearing loss) for older adults with any stage solid tumor malignancies starting a new chemotherapy regimen, this model stratifies patients into low‐risk, medium‐risk, and high‐risk categories for severe chemotherapy toxicity, and it is superior to the clinician‐rated Karnofsky performance scale for identifying older adults at risk. 3 , 21 The CARG measure takes less than 5 minutes to administer and facilitates patient–provider discussions about the relative risk of serious toxicities across various therapy regimens. A modified CARG measure can help identify patients at high risk of toxicity‐related hospitalizations 22 and falls. 23 Although the CARG toxicity tool has been validated in other populations (e.g., a multiethnic Asian population in Singapore 24 and older adults in Japan 25 ) and in patients with specific cancer types, 26 , 27 some studies suggest that the CARG toxicity tool may not be equally predictive of toxicity in all populations. 28 These differences may be related to how treatment decisions occur in different health care systems, highlighting the need to understand the value of the tool in disparate populations.

The CARG breast cancer tool was specifically tailored for patients with localized breast cancer and considers specific factors for breast cancer therapies in addition to the comprehensive clinical and GA variables. 29 This risk‐prediction model allows for a more targeted estimate of chemotherapy toxicity in this population subset. Studies indicated that higher risk groups had higher rates of hospitalization during the course of therapy as well as reduced dose intensity, 29 which compromised treatment efficacy. 30

The Chemotherapy Risk Assessment Scale for High‐Age Patients (CRASH) is another model that focuses on predicting severe chemotherapy toxicity and determining the appropriateness of chemotherapy in older adults. 31 Developed by Extermann et al., CRASH assigns patients with hematologic and nonhematologic malignancies to four risk categories (i.e., low, mid‐low, mid‐high, and high) based on age‐related factors and GA parameters (e.g., cognition, nutritional status, and instrumental activities of daily living [IADLs]). This battery is slightly longer, because it incorporates full measures rather than individual question items, averaging 20–30 minutes to administer and calculate. 31 The CRASH model included older patients with hematologic malignancies, as opposed to the CARG model, which only included those with solid tumors during its development. 32

These three prediction models vary in scope, variables considered, and target population. The CARG tool evaluates general factors like age, sex, and performance status and applies to a broad range of patients with solid tumor malignancies. Subsequent studies also found that the CARG tool may predict toxicities in lymphoma and multiple myeloma. 33 The CARG breast cancer model focuses on patients with localized breast cancer receiving adjuvant or neoadjuvant regimens. The CRASH model applies to older patients with both solid tumor and hematologic malignancies. Despite their differences, each model identifies GA variables as useful predictors for treatment toxicity. 34 Similar GA domains were associated with treatment toxicity across all models, such as fall history and physical function. Each model was developed and validated in independent, unique cohorts for predictive performance, and clinicians should choose a model for toxicity prediction that is the most appropriate for the specific characteristics of their patients ( Table 1 ).

GA FOR PREDICTING OUTCOMES IN OLDER ADULTS WITH SPECIFIC HEMATOLOGIC MALIGNANCIES

It is well established that GA can predict the outcomes of older adults with various hematologic malignancies ( Table 2 ). 35 – 45 Given variability in disease course and treatment regimens in hematologic malignancies, several risk‐prediction scores using GA variables have been developed ( Table 3 ). 41 , 43 , 46 – 58 In each setting, GA variables help to better discriminate risk versus treatment benefit. Across studies, the importance of assessing function and comorbidity is consistently demonstrated, although specific measures and outcomes may differ by disease setting or treatment intensity. For example, the Fondazione Italiana Linfomi incorporated GA into the International Prognostic Index to generate the Elderly Prognostic Index, which better predicts outcomes among older patients with diffuse large B‐cell lymphoma (DLBCL). 53 Specifically, the Elderly Prognostic Index incorporates age, comorbidities, functional status, and disease‐specific features (e.g., stage, lactate dehydrogenase level, number of extranodal sites) and categorizes patients into three risk groups: low, intermediate, and high. The higher risk categories are associated with worse overall survival. In myelodysplastic syndrome (MDS), specific frailty indices have been developed. 48 , 50 For example, the 15‐item MDS‐specific frailty index incorporates variables such as fatigue, assistance with food preparation, and 4‐meter walk time, and greater frailty is associated with worse overall survival. In multiple myeloma, one common risk classification is the International Myeloma Working Group frailty score, which incorporates age, comorbidities, and functional status to categorize patients as fit, intermediate, or frail. Risks of toxicity and mortality were higher in the frail group, followed by the intermediate and fit groups. 43 Other risk‐prediction scores generally focus on comorbidities (e.g., the Hematopoietic Cell Transplantation Comorbidity Index, the Acute Myeloid Leukemia‐Composite Model) 57 or adapt existing frailty indices, which may or may not include additional variables, such as functional status or disability, to increase disease specificity (e.g., the revised Myeloma Comorbidity Index). 51 , 59 Efforts are ongoing to incorporate GA into some established comorbidity indices to improve risk stratification. 60 In practice, routine collection of activities of daily living (ADLs), IADLs, and comorbidity burden can facilitate the implementation of several risk‐prediction models for older adults with hematologic malignancies.

GA FOR TREATMENT DECISION MAKING

GA is useful when considering cancer‐directed treatment or selecting patients in certain risk categories for innovative treatment approaches. In a systematic review of 61 studies, it was observed that GA changed the treatment course in 31% of patients (range, 7%–56%), typically to a less intensive option. 61 This process has been studied in several cancer types, including lung cancer, pancreatic cancer, acute myeloid leukemia, and lymphoma. 62 – 65 In lung cancer, the Elderly Selection on Geriatric Index Assessment study (ESOGIA‐GFPC 08‐02) randomly assigned adults aged 70 years and older with an ECOG PS of 0–2 and stage IV nonsmall cell lung carcinoma to GA‐guided treatment versus standard of care. 62 Survival was not different between arms, but those who received GA‐guided treatment had lower rates of toxicities. In addition, the patients who received GA‐guided treatment had a longer treatment failure‐free survival (time until treatment discontinuation for any reason, including disease progression, treatment toxicity, or early death). In lymphoma, the R‐CHOP versus R‐mini‐CEOP in Elderly Patients with DLBCL (ANZINTER3) study ( ClinicalTrials.gov identifier NCT01148446 ) selected patients older than 65 years with an ECOG PS of 0–3 and stage II–‐IV DLBCL who were fit based on ADLs, comorbidities, and the presence/absence of geriatric syndromes. 63 Patients were randomly assigned to standard‐dose R‐CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) or the less intensive R‐mini‐CEOP (rituximab plus cyclophosphamide, etoposide, vincristine, and prednisone). Outcomes were similar between groups; those older than 72 years with low‐risk disease had better outcomes with the less intensive approach. 63 Other studies investigating GA‐guided treatment approaches are ongoing. 66

GAM TO IMPROVE OUTCOMES

Older adults often prioritize outcomes like physical function, cognition, and quality of life over longevity. 67 – 69 The utility of GA is not limited to informing therapeutic decision making; it can also guide management interventions to mitigate identified vulnerabilities, because these vulnerabilities are often what older adults care most about. For example, a patient who has falls with decreased physical function on GA could be referred for balance training with a physical therapist; if the home environment is suspected to be unsafe, a home evaluation could be initiated with recommendations for environment modification. A systematic review of 61 studies found that nononcologic interventions were recommended in over 70% of patients receiving GA, most commonly with a focus on social supports, nutrition, and polypharmacy. 61 A positive effect on treatment completion was seen in the majority of studies, and treatment‐related toxicities and complications were reduced with the use of GA. In addition, GA improved communication and led to more goals‐of‐care conversations. In a systematic review and meta‐analysis of 17 randomized controlled trials (RCTs) of GAM, it was found that the risk of treatment toxicity was significantly lower in the intervention group. 70 However, no differences in mortality risk, hospitalization, or modification of cancer therapy (early treatment discontinuation or dose reduction) were observed. 70 The model of GAM care delivery varied across studies; different models of care are discussed further below.

Two general approaches are used to integrate GAM with oncology care: (1) direct involvement of geriatric specialists with either a co‐management model or multidisciplinary case review to inform recommendations, and (2) automatically generated recommendations tailored to GA impairments (i.e., independent of a geriatrics professional) provided to oncology teams for review and implementation. Variability among models of GAM is inevitable, and the best model will depend on clinical setting, available resources, and other factors. Below, we review studies that have evaluated GAM, describing the specifics of trial design, intervention delivery, and outcomes ( Table 4 ). 71 – 78 Collectively, these studies indicate the value of GAM for identifying and addressing medical, functional, and psychosocial issues that could otherwise go unnoticed by oncology care teams, enabling clinical teams to proactively intervene to optimize treatment outcomes and enhance quality of life.

Direct geriatric specialist involvement

The Geriatric Assessment‐Driven Intervention (GAIN) study ( ClinicalTrials.gov identifier NCT02517034 ) was a single‐center, randomized clinical trial of patients aged 65 years and older initiating a new chemotherapy regimen ( N = 605) for solid tumors of any stage with a primary outcome evaluating whether a GA‐driven intervention can reduce chemotherapy‐related toxic effects in older adults with cancer. 71 Patients underwent initial GA and were then randomized (2:1) to either the intervention (GAIN) or usual care. In the intervention arm, the GA was reviewed by a geriatrics‐trained multidisciplinary team, including an oncologist, nurse practitioner, social worker, physical/occupational therapist, nutritionist, and pharmacist, and GA‐guided interventions were implemented based upon predetermined thresholds for GA domain impairments. In the usual care group, GA results were shared with the oncology teams, but interventions were not facilitated by the study team. Most patients were female (59%) with advanced solid tumor malignancies (stage IV, 71.4%). The GAIN intervention significantly reduced severe chemotherapy toxicity by 10.1% (grade 3–5 toxicity in 50.0% of the intervention group vs. 60.6% of the control group; p = .20) and increased advance directive completion (28.4% vs. 13.3%, respectively; p < .001). Of note, no differences in overall survival or hospitalizations were observed.

The Effect of Geriatric Intervention in Frail Elderly Patients Receiving Chemotherapy for Colorectal Cancer (GERICO) study ( ClinicalTrials.gov identifier NCT02748811 ) was a single‐center, randomized, phase 3 study evaluating the benefit of GA with targeted interventions in adults aged 70 and older ( N = 142) receiving adjuvant or first‐line palliative chemotherapy for colorectal cancer on chemotherapy completion (primary outcome). 72 Importantly, the GERICO study limited inclusion to older patients with a Geriatric‐8 (G8; a screening tool) score of ≤14, thus representing a more vulnerable/frail population. All patients underwent baseline GA at the time of treatment initiation, and the intervention group received GA‐targeted interventions based upon predetermined GA domain thresholds, including medication adjustment (62%), nutrition referral (51%), and physiotherapy (39%). A higher proportion of patients in the intervention arm completed their chemotherapy regimen compared with the control arm (45% vs. 28%; p = .04). Severe toxicity occurred in 39% of patients in the control group versus 28% in the intervention group ( p = .16). Overall improvements in quality of life (as measured by decreased burden of illness) and mobility were observed in the intervention group ( p = .048 and p = .008, respectively). No difference in overall survival was observed.

The Integrated Geriatric Assessment and Treatment Effectiveness (INTEGRATE) trial (Australian New Zealand Clinical Trials Registry number ACTRN12614000399695) was a multicenter RCT examining the effect of integrated geriatrician consultation and support for adults aged 70 and older with solid tumor malignancies or DLBCL initiating a new line of chemotherapy, targeted therapy, or immunotherapy ( N = 154), with a primary outcome evaluating intervention effects on health‐related quality of life (as measured by the Elderly Functional Index, which focuses on functional domains). 73 Patients in the intervention group received GA with integrated oncogeriatric care, in which a geriatrician consulted at baseline, 12 weeks, 24 weeks, and as needed. The intervention delivery was a personalized management plan and was not predefined by study protocol. Patients in the control arm received educational information and encouragement about exercise/nutrition but did not receive integrated oncogeriatric care. The intervention group had improved Elderly Functional Index scores over a 24‐week period (overall main effect of group, p = .04) as well as fewer unplanned hospitalizations (multivariable‐adjusted incidence rate ratio, 0.60; p = .007) and a lower frequency of early treatment discontinuation due to toxicity on exploratory analysis ( p = .001). There were no differences in treatment modification or overall survival.

Other smaller, randomized trials have not demonstrated a benefit from GAM. Orum et al. 74 conducted an RCT evaluating the benefit of a tailored GA intervention follow‐up by a geriatric multidisciplinary care team (geriatrician and geriatrics‐trained nurse) for 90 days after initial GA among patients with head and neck, lung, upper gastrointestinal, or colorectal cancer ( N = 363), with a primary outcome evaluating adherence to cancer treatment. All participants received GAM recommendations at baseline; subsequently, patients classified as vulnerable or frail were randomized to receive the tailored GA intervention follow‐up versus no tailored follow‐up. The tailored follow‐up consisted of periodic visits (in person or on the phone) with the geriatric multidisciplinary care team, during which new interventions could be initiated or prior interventions adapted, including pharmacologic, nutritional, physical, or social modifications (i.e., GAM). There were no differences noted between groups in adherence to cancer treatments, rates of hospitalization, or functional decline. One potential explanation is that the effect of the GAM‐tailored follow‐up was limited because all participants received GAM after the baseline GA and before randomization.

The Comprehensive Geriatric Assessment and Management for Canadian Elders with Cancer study (5C Trial; ClinicalTrials.gov identifier NCT03154671 ) evaluated the impact of GAM on outcomes in adults aged 70 years and older with solid tumor malignancy, lymphoma, or myeloma receiving first‐line or second‐line chemotherapy and/or immunotherapy ( N = 350), with a primary outcome evaluating quality of life. 75 The GAM intervention was a standardized protocol aligning with the ASCO geriatric oncology guidelines, in which a clinical team completed the GA and implemented predefined, evidence‐based interventions deemed relevant by the intervention team together with the participant. The 5C Trial did not observe differences in quality of life, unplanned hospitalizations, toxicity, or survival with GAM, although investigators noted that most participants received GAM recommendations on or after treatment initiation, which may have mitigated any differences in effects. In addition, the study was conducted during the coronavirus disease 2019 (COVID‐19) pandemic, which may have influenced the primary outcome of quality of life for this study.

Randomized trials focusing specifically on hematologic malignancies are limited. One RCT evaluated the impact of an embedded geriatric consultation in conjunction with a hematologic oncologist versus usual care for patients aged 75 years and older with lymphoma, leukemia, or multiple myeloma ( N = 160), with a primary outcome assessing overall survival. 79 Only frail patients and those deemed at risk for frailty, as determined by deficit accumulation and phenotypic frailty approaches, were subsequently randomized. No prespecified interventions were required, although recommendations could be communicated to the patient’s primary care physician, including referrals to psychiatry or physical therapy. There was no difference in 1‐year overall survival between the intervention and usual care groups. However, those in the intervention arm had increased end‐of‐life goals‐of‐care discussions. Hematologists were surveyed about the benefits of geriatric consultation, and the majority rated the consultation as useful in the management of several geriatric domains.

GAM interventions independent of a geriatric clinician

The Geriatric Assessment for Patients 70+ study (GAP70+; ClinicalTrials.gov identifier NCT02054741 ) led by Mohile et al. was a cluster‐randomized trial conducted in community oncology practices. 77 Patients aged 70 years and older with advanced solid tumor malignancy or lymphoma were enrolled across 40 community oncology practice sites in the United States. Eligible patients were initiating a high‐risk cancer regimen (any line, ≥50% risk of toxicity) and had at least one GA domain impaired. Practice sites were randomized to intervention or usual care. Although all patients underwent GA, only those at intervention sites had the results and GA‐guided management recommendations shared with the oncology team ( Figure 1 ). GA‐guided recommendations were determined by an algorithm and offered when a patient’s scores met predetermined thresholds. Oncology teams were responsible for prioritizing and implementing recommendations. Patients in the control arm (i.e., usual care) did not receive a GA summary or recommendations, although oncologists received alerts for positive screens for impaired mood or cognition. The primary outcome was clinician‐rated toxicities, which were markedly reduced in the intervention arm (50%) compared with the control arm (70%). Patient‐reported toxicities were also reduced. 80 No changes in overall survival were observed, but patients in the intervention arm had fewer falls and improvements in polypharmacy (i.e., more medications discontinued, as measured by a medication log completed by staff). Patients in the intervention arm were more likely to have a primary dose reduction (e.g., initial cycle administered at reduced dose) 81 ; nevertheless, no difference in overall survival between the two groups was observed. 77 Figure 1 depicts the GAM care delivery intervention used in the GAP70+ study, which is particularly relevant for clinicians who do not have access to geriatrics experts in their practice; the management recommendations were implemented only for patients with an impairment in that specific geriatric domain.

The Communication on Aging and Cancer Health study (COACH; ClinicalTrials.gov identifier NCT05349227 ) had a GA intervention design similar to that of the GAP70+ study and evaluated the influence of GAM on aging‐related communication and satisfaction with care. 78 This trial enrolled patients aged 70 and older who had advanced solid tumor malignancy or lymphoma and at least one GA domain impairment from 31 community oncology practice sites in the United States. The COACH study demonstrated that the GA intervention improved communication about aging‐related conditions in the context of oncology care, both quantitatively, through improved patient and care partner satisfaction with communication, and qualitatively, through analyses of clinical encounter transcripts demonstrating an increase in conversations about aging‐related concerns.

Practical GA

In 2023, the ASCO guidelines for the care of older adults with cancer receiving systemic therapy were updated to reflect the latest evidence about GAM from large RCTs. 10 , 71 , 77 , 78 These studies clearly demonstrated that serious toxicities from systemic therapy can be reduced without compromising overall survival. GAM leads to decreased falls, more medications discontinued, higher rates of advance directive completion, and improved patient and caregiver satisfaction. The new guidelines reflected these findings by recommending GAM as the standard of care for older adults starting new therapies (chemotherapy, targeted therapy, and immunotherapy), specifying that GAM must assess the essential geriatric domains (physical function, cognitive performance, emotional health, comorbid conditions, polypharmacy, nutrition, and social support). In short, all adults older than 65 years should have their management guided by GA to implement better decision making and to appropriately offer aging‐sensitive supportive care interventions as part of routine care to avoid both undertreatment (of fit older adults) and overtreatment (of frailer older adults).

Unfortunately, the uptake, implementation, and integration of GA in oncologic care remains low. 20 , 82 A recent large international survey revealed that as few as 22% of oncology providers regularly used d GA in the management of older adults with cancer. 20 Greater than 75% of providers agreed that GA was important, that evidence supported its use, and that it should be used to assess older adults. However, they identified barriers to implementation that precluded its use, including lack of support staff, time, and knowledge and uncertainty about which GA tool(s) to use. These concerns fall into two general areas: (1) concerns about knowledge or training and (2) concerns about resources or time. Although all providers expressed concerns about the latter, those providers who were unfamiliar with the ASCO guidelines expressed much greater concerns about the former. Fortunately, both types of barriers can be addressed.

To overcome barriers, the Older Adults Task Force of the ASCO Health Equity and Outcomes Committee (Task Force) proactively created tools, trainings, and strategies to accompany the release of the guidelines. To minimize resource constraints and burdens on providers, the Task Force developed a PGA tailored for use in routine clinical practice by oncologists informed by focus groups with community‐based providers. Based on previously published formal consensus development work on the necessary domains of GA in oncology, the Task Force created a simplified and predominantly patient‐reported tool using a consensus development approach in collaboration with CARG. 83 Multiple validated tools for each GA domain were compiled and reviewed for inclusion in the new simplified tool, and ultimately those best‐suited for routine clinical care were chosen. The chosen instruments were compiled, reviewed, and approved by CARG membership and the Science and Education Committee of SIOG. The resulting PGA ( Table 5 ) 3 , 21 , 29 is a set of patient‐reported measures and four additional items completed by providers or staff that takes only 10–25 minutes to complete. Specific score cutoffs are provided as is an action chart, which ties the tools to appropriate actions to be taken (e.g., referrals, dosing considerations). These elements ensure that outcomes will be meaningfully affected by the PGA, optimizing care by avoiding overtreatment and undertreatment. 84 Management recommendations based on identified impairments were included in the most recent ASCO guideline update. 10 , 85 Whether it will improve uptake of GA in general oncology practice will require future validation and follow‐up.

STRATEGIES TO OVERCOME IMPLEMENTATION BARRIERS

Barriers to routine GA implementation include lack of knowledge of guidelines supporting GA implementation, lack of time, staff turnover, and competing institutional priorities. 20 , 86 Lack of effective referral pathways to multidisciplinary care professionals to support GA and help address identified concerns are also obstacles to GA implementation. 87 , 88 Because patients are often overwhelmed at initial diagnosis and treatment planning, they may not be willing to set up the additional appointments that may be needed to implement GA recommendations. 89

Despite these challenges, a growing body of literature demonstrates the feasibility of integrating GA into routine oncologic practice. Even in busy and diverse oncology practices, GA can be adapted for practical use, 10 even under circumstances in which treatment decisions need to be made quickly, such as in acute myeloid leukemia. 90 – 92 Most older patients can complete the self‐administered assessments without assistance. In a study evaluating the feasibility of a cancer‐specific GA in the academic oncology setting, the mean time to completion was 27 minutes, and most patients were satisfied with the length of the questionnaires. 9 The feasibility of incorporating GA into community oncology clinics 93 and oncology clinical trials, including within cooperative group settings, 92 , 94 has also been demonstrated. Below, we discuss evidence‐based strategies for GAM implementation.

GA screening tools

As discussed above, the PGA is a brief but comprehensive measure that community oncologists at ASCO believe can be more easily implemented than longer GAM interventions tested in RCTs. Nevertheless, because the uptake of GA in the oncology setting has remained limited despite mounting evidence, researchers have attempted to identify brief screening mechanisms that can identify those vulnerable older adults with cancer who are most likely to derive benefit from GA. A recent systematic review of 12 screening tools determined that the G8 95 and the Vulnerable Elders Survey‐13 (VES‐13) 96 were the measures with the greatest evidence supporting their use; the G8 showed higher sensitivity and the VES‐13 showed greater specificity for identifying patients who would benefit most from a full GA. 97 The VES‐ 13 is self‐reported, whereas the G8 can be both self‐reported or administered by a provider. 95 , 98 They both require 5 minutes or less to complete. 99 In addition to identifying patients who may benefit from a more comprehensive GA, these screening tools have been shown to predict risks of toxicity, functional decline, and decreased progression‐free and overall survival in various hematologic and solid tumor malignancies. 54 , 100 , 101 There is growing evidence that screening tools may be less effective at guiding care delivery than full GA, 102 but these tools remain options for oncologists who are not trained in geriatrics and practice in resource‐limited settings.

Engaging the oncology workforce to deliver GAM

Strategies and initiatives to improve the implementation of GAM and its principles into practice have been published. However, most of the reported examples have consisted of the experiences of individuals at their own institutions 103 , 104 or larger initiatives like those summarized by the Latin America Cooperative Oncology Group, 105 each working to overcome unique barriers and challenges to implementation. Overcoming implementation barriers requires strategies that address the capability, opportunity, and motivation of clinical teams, leading to behavior change, also called the COM‐B model of behavior . 106 Guided by the behavioral change wheel, 106 we suggest strategies to overcome common implementation barriers (see Table S1 ). The implementation barriers and strategies discussed below do not represent an exhaustive list and are often used in combination.

Education on GA and guidelines overcomes several barriers by addressing psychological capability and reflective motivation. A common barrier is lack of awareness of guidelines supporting routine GA implementation for patients aged 65 years and older who are considering systemic therapy. Education about GA can also address the misconception that GA is too time‐intensive by focusing on the actual time required to assess its various components. During the education session, the learner is pushed to reflect on how restructuring an initial patient assessment to include GA may have a minimal impact on time. When GA education is embedded into routine onboarding procedures, this strategy also addresses the barrier of staff turnover.

Training on GAM addresses implementation barriers by imparting knowledge about the importance of GA implementation, which increases physical and psychological capability. As clinical teams become more comfortable with GA administration, scoring, and interpretation, the amount of time required to do these steps will decrease. As comfort increases, the belief that the amount of time required to implement GA is too great will also decrease. Incorporating routine training on GA and GA‐guided management recommendations also addresses staff turnover.

Restructuring the electronic health record (EHR) can affect the clinical workflow and create physical opportunities to implement GA. EHR modifications include prompts, templated notes or data collection forms, and clinical decision supports to identify GA‐guided recommendations. These EHR modifications address the barrier of time by making GA administration, scoring, and interpretation more automatic, and they serve as reminders to the clinical teams to implement GA. A study by Harmon et al. 107 demonstrated success with this strategy; patients completed a self‐reported, web‐based GA before their appointment, and any impairments, along with recommended interventions, were displayed in the patients’ EHR; >75% of patients ( n = 266) completed the web‐based GA before their clinic appointment. We discuss this strategy in more detail below.

Reworking the clinical workflow enables clinical teams to implement GA into their existing workflow in a manner best suited to the setting. Implementation strategies that serve as enablement interventions work by addressing clinical teams’ physical capability, psychological capability, automatic motivation, and physical and social opportunities. To rework the clinical workflow, it is also important to identify clinical champions who represent the various team members, including physicians, advanced practice providers, nurses, medical assistants, and administration. We and others have utilized clinical workflows that have engaged multiple members of the clinical team ( Figure 2 ).

Identifying/training clinical champions and forming implementation teams address barriers around the lack of support staff, which also contributes to the barrier of time. Clinical champions then need to form an implementation team to work through the phases of implementation: (1) exploration, (2) preparation, (3) implementation, and (4) sustainment. During the exploration phase, implementation teams review existing assessments and clinical algorithms for their patients. For instance, cancer centers may already routinely assess the risk of falls to identify patients who may need additional assistance during the clinic visit. However, they may not be routinely counseling patients and their care partners more broadly about falls prevention. The implementation team can then raise awareness of this service gap. During the preparation phase, the implementation team sets up education and training for the initial roll‐out and, as part of future onboarding, makes EHR modifications, proposes a new clinical workflow with integrated GA implementation, and obtains feedback from clinical teams and administration. During the preparation phase, implementation teams need to have routine communication with frontline staff and administration. During the implementation phase, the implementation team needs to monitor the implementation process using audit and feedback and continuously modify processes accordingly. They must track whether GA and GA‐guided recommendations are being routinely implemented. During the sustainment phase, the implementation team monitors the impact of implementing GA on key outcomes. They may need to take additional steps to expand clinical teams and coordinate across service lines to realize the full benefits of GA implementation.

Resources are available to help, such as the Clinical Implementation Core (CIC), which is part of CARG. 108 Although the CIC’s focus is on providing a framework for geriatric oncology care delivery, it also provides an opportunity for practitioners to bring their individual inquiries, at any phase of implementation, to the CIC for advice and collaboration. Other organizations, such as SIOG and the Association of Community Cancer Centers, also provide opportunities for education and strategies for implementation. All of these organizations have resources that can be accessed through their websites.

GA and technology

New frontiers in data science and technology could enable easier collection and analysis of GA data; improve care access and communication pathways between older patients, caregivers, and clinicians; and facilitate integration of GA data with other data sources (e.g., the EHR, claims data, sensors from wearable devices) to create a trove of real‐world data to address the evidence gap in older adults with cancer. 109 Although the paper‐and‐pencil format of GA has primarily been evaluated, the feasibility of a computer‐based GA has also been demonstrated. 110 One of the oft‐cited barriers to technology use in the care of older adults is the digital divide , whereby older adults report less access, usage, and facility with digital information and communication technologies (ICTs) than younger adults. 111 However, this gap is closing, accelerated by increased reliance on ICTs during the COVID‐19 pandemic, 112 and the aging of successive generations with increasing digital literacy is likely to further reduce this barrier. Adoption of ICTs is increasing rapidly in older adults: from 2012 to 2021, the percentage of adults older than 65 years who owned a smartphone increased from 13% to 61%, and ownership of tablet computers increased from 6% to 44%. 113 Most older adults (75%) report using the internet regularly, and 64% report having broadband connections. 114 Patient portal 115 and mobile application use 116 have also increased rapidly in older adults.

Increased ICT access and utilization among older adults with cancer offers opportunities to capture patient‐reported GA data digitally and remotely. Successful platforms often have a patient and clinician interface, questions are brief and simple, and functionality is co‐designed with stakeholders to ensure feasibility and usability. 107 , 117 – 120 In addition to the collection of GA data, these platforms provide interpretations and recommendations, often for clinicians and occasionally for patients, to facilitate shared decision making and supportive care interventions. Resources (e.g., staff, education) to support the completion of GA electronically are critical to implementation. Digital capture of discrete, structured data elements from GA (such as numeric scores and responses) with integration into the EHR facilitates clinical review and decision making as well as the creation of larger data sets for research. One example of such successful implementation is at the University of Rochester Medical Center, which uses EHR‐integrated GA tools with autoscoring and interpretation, where feasible. 121 The patient‐reported elements of GA are distributed as surveys through the EHR patient portal before patients appointments.

GA and telemedicine

The use of telemedicine to deliver GA is an effective approach and has been explored across various health care settings. 122 – 126 Telemedicine can help to overcome barriers to access and implementation for GAM as well. 107 , 122 , 127 Telemedicine facilitates completion of GA (e.g., virtual Short Physical Performance Battery, Short Orientation‐Memory‐Concentration Test), 128 enables clinicians to communicate recommendations to patients and caregivers remotely, and promotes access to supportive care interventions (e.g., dietitians, physical therapists). 128 , 129 Telemedicine provides flexibility for GA to be completed asynchronously (e.g., a pharmacist may conduct a medication assessment before or after the GA clinical visit). GA through telemedicine is especially attractive for settings in which access to geriatric specialists is limited, such as in community oncology practices, and for patients who face barriers to care, such as long‐distance travel. 122 – 124 Hybrid telemedicine models have also been tested in which GA is completed remotely, and subsequent clinical visits consist of a mix of in‐person and virtual consultations. 127 , 130 Telemedicine can also facilitate oncogeriatric tumor or other multidisciplinary team meetings. 131

GA and mobile health

In addition to telemedicine, other digital data sources can augment care and decision making for older adults with cancer. An increasing number of wearable health technologies passively capture and analyze data reflecting activity level, gait, vital signs, and sleep. Patients can actively track nutrition, symptoms, activity, and other patient‐reported measures through mobile applications or other electronic devices, and recommendations can be provided based on these data. 132 – 135 For example, several studies have demonstrated the feasibility of measuring physical activity levels using a smartphone, activity tracker, or accelerometer; and these data can be used to identify chemotherapy toxicity and various symptoms as well as to deliver personalized exercise recommendations. 133 – 135 Older patients tracking patient‐reported measures can trigger alerts indicating moderate or severe symptoms, allowing for subsequent management; such interventions have been shown to improve quality of life and health care utilization. 136

Advanced data analytics for older adults with cancer

In recent years, rapid advances have taken place in both computational capacity and data‐analytic approaches. Large leaps in high‐performance computing (e.g., computer chips, networking technology, and distributed computing) have enabled broader access to the technology needed to perform advanced analytics, including machine learning and artificial intelligence (ML/AI) approaches. The most advanced ML/AI approaches, such as deep learning, require vast data sets and high‐performance hardware. These approaches can simultaneously incorporate and analyze all the data we are now able to collect from older patients with cancer, including data from GA, the EHR, claims, sensors, and self‐report; images, documents in natural language, and audio data could also be accommodated using these methods. ML/AI methods are already being used to generate predictive and prognostic models for older adults with cancer. 137 , 138 These models are likely to become more powerful and informative as well as updateable with new information. One of the feasible future applications using these methods is the digital twin : a digital simulation of an individual older patient, incorporating all known information, could be used to simulate the effect of treatments, predict outcomes, and remotely monitor symptoms for that patient. 139

A main barrier to achieving these breakthroughs is the lack of infrastructure to support them. Although the federal government is attempting to enforce FAIR ( findable, accessible, interoperable, and reusable ) data in health care, 140 , 141 it is challenging to assemble the large, multisource data sets needed to create digital twins or other large predictive models. 139 For example, data sharing and merging between EHR systems is still inadequate, even between systems that use the same EHR vendor. In addition, vast investment and effort will be needed to make sure the data are accurate, timely, consistent, and secure. Ethical concerns also arise around the use of data and ML/AI methods encompassing privacy and equity (e.g., algorithmic bias, access to AI technologies, and lack of transparency/interpretability). 142

GA FOR DIVERSE POPULATIONS

The older adult population in the United States continues to increase in racial and ethnic diversity, with the number of older Black adults expected to triple and the number of older Latino adults expected to quadruple by 2060. 143 Nevertheless, pervasive structural racism continues to result in higher mortality among minoritized populations. 144 The balance of cancer treatments, systemic causes of inequities, and social drivers of health need to be carefully evaluated because of their synergistic negative effects on clinical outcomes among marginalized populations. 145 – 153 Social inequity drives increased psychosocial stress, the effects of which compound over time and contribute to health inequities in minoritized populations. 154 , 155 GA has the potential to formalize the assessment of social determinants of health, which is critical for clinical decision making.

Equitable implementation of GA among minoritized older adults

Although clinical trials implementing GA have resulted in increased patient enrollment 71 , 77 and wider geographic distribution, 78 racial diversity in these trials remains insufficient. In large academic center studies of older adults with cancer receiving GA‐guided care across various stages of cancer and tumor types, 76%–87% were White. 71 , 77 Of 500 older patients enrolled in community clinical sites across 15 states who received GA, 89% were White. 78

There is a particular need for practical approaches to the implementation of GA in rural, under‐resourced, and isolated areas that serve vulnerable patients. In some practices, greater than 20% of older adults with cancer travel at least an 1 hour each way to receive care. 156 Further studies on GA implementation should consider neighborhood‐level and community‐level social determinants of health, including transportation security, housing security, and rurality. Examples of resources that evaluate these factors are the Community Need Index 157 the Area Deprivation Index, 158 and the Social Vulnerability Index. 159

Language barriers among minoritized older adults with cancer

A significant challenge faced by diverse older adults is a language barrier, which can result in poor or absent patient–provider communication critical to treatment planning and coordination and poor quality of care, poor adherence to treatment, and safety concerns. 144 , 160 About 26 million people in the United States report speaking English less than very well or have limited English proficiency (LEP) and thus experience inequities in accessing and using health services because of language; notably, greater than one third are aged 55 years and older. 161 Latino and Asian‐origin populations make up the majority of the LEP population; these are also the patients likely to experience linguistic and cultural barriers that can impede timely treatment and care. 161 The COVID‐19 pandemic highlighted the significant gap between English‐proficient patients, who were able to pivot to telemedicine for their cancer care, and Asian‐origin and Spanish‐speaking patients, who experienced significantly lower odds of telemedicine use. 162 , 163

Equitable access to quality language services remains incremental and fragmented, regardless of modality. 164 , 165 A 2023 review exploring cancer treatment decision making among older adults with LEP found that medical mistrust and perceived discrimination by providers were the primary drivers of differences in treatment decisions among patients with LEP. 166 In addition, this review found that respondents expressed concerns about language barriers, financial burden, and insurance. These barriers can lead to gaps in obtaining and acting on critical information from their providers. 167 GA interventions can potentially ensure that patient preferences are clearly established within the context of social, clinical, and personal factors that are key for patient‐centered care. 10 In the COACH trial, communication between patients and their providers improved after GAM. 78 Although those participants were primarily White and English‐proficient, tailored GA recommendations may also improve communication for older adults with LEP.

To address persistent and compounded inequities, representation in clinical research is vital to ensuring that the aging‐related needs of racially, ethnically, culturally, and linguistically minoritized older adults with cancer are appropriately addressed. 155 , 168 A recent scoping review analyzing 59 publications on health disparities among older adults with cancer who belonged to minoritized groups found that, although research in this area is increasing, the literature is largely descriptive rather than solution‐driven. 169 Future work on social factors and the importance of integrating social needs in cancer care must require greater inclusion of more diverse populations. In a recent publication by the National Academy Press, a committee dedicated to greater integration of these factors proposed five tasks to strengthen social care in health systems to address social determinants of health among patient populations: awareness , adjustment , assistance , alignment , and advocacy . 170 The implementation of GAM for diverse populations may require a similar approach. Equitable implementation requires awareness , adjustment , and assistance to occur within health care systems to integrate social measures while implementing GAM into oncology care. 171 – 174

ADDRESSING THE NEEDS OF CAREGIVERS OF OLDER ADULTS WITH CANCER

In the United States, most caregivers of older adults with cancer are female family members who spend nearly 33 hours per week on average providing care. 175 , 176 Their responsibilities range from treatment decision making to managing end‐of‐life care and frequently include delivering nursing care without training. 177 Caregivers also assist with patient self‐care, provide emotional support, and manage household tasks with limited social support. 175

Multiple studies have demonstrated that cancer caregiving affects caregiver psychological health and physical well‐being. 178 , 179 Caregiver burden is defined as the extent to which caregivers perceive the adverse effect that caregiving has on their emotional, social, financial, and physical functioning. 180 Given the level of care that is required by older adults with cancer, who often have comorbidities and aging‐related conditions, caregivers experience substantial physical and emotional challenges that can lead to caregiver burden. 181 , 182 Caregivers of patients with GA impairments in ADLs and/or IADLs report greater emotional distress. 176 , 178 , 182 Caregivers of older adults with cancer also tend to be older (aged 63–66 years on average) with their own health issues and geriatric syndromes. 181 – 183 Compared with noncaregivers of the same age, caregivers of older adults with cancer are more likely to experience deterioration in physical health, have poor health‐related behaviors, and are less likely to engage in preventive care. 184 – 187 Caregiver burden is associated with negative caregiver health effects, including increased all‐cause mortality, and affects the caregiver’s ability to provide care, resulting in increased risk of patient hospitalization and more intensive and/or inappropriate end‐of life care. 185 , 188 , 189

Validated caregiver distress screening tools are available, 190 , 191 and Shaffer et al. observed that administering the CancerSupportSource‐Caregiver, a validated electronic distress screening program for cancer caregivers, was feasible and well accepted. 192 However, only limited implementation of these tools into clinical practice has occurred. Kadambi et al. recently demonstrated that it is feasible to administer GA to assess the health and supportive care needs of older caregivers of older adults with cancer. 183 GA helped to identify aging‐related conditions that might influence caregiving ability and guide supportive care interventions.

There have also been numerous supportive care intervention studies for cancer caregivers, both in‐person and virtual, targeting caregivers and their families, that have focused on interpersonal interventions, problem solving or skill building, psychoeducational interventions, subspecialty palliative care, and supportive therapy. 193 – 195 Although most studies have been small, included mainly younger White caregivers, and had limited diversity, they demonstrated small to medium beneficial effects on caregiver burden, coping, self‐efficacy, and quality of life. A recent systematic review of these studies noted that the interventions were not designed in a way that is easy to translate into clinical practice. 193 A recent report of a caregiver stakeholder workshop involving 15 cancer caregivers identified five main supportive care areas: (1) information and training about cancer and treatment, (2) caregiver integration into the patient’s health care delivery system, (3) assistance with navigating the health care system, (4) focus on caregiver health and well‐being, and (5) policy reform to address caregivers’ unmet needs. 196 Future research should focus on how to address the needs of caregivers of older adults with cancer through appropriate assessment of caregiver burden and through care coordination with GAM with the goal of improving outcomes of both caregivers and patients.

Summary

The field of geriatric oncology has made tremendous strides over the past few decades to improve outcomes for older adults with cancer. The field has demonstrated the importance of GA in identifying aging‐related impairments that influence cancer‐related outcomes and the feasibility of incorporating GA into routine clinical practice. More recently, using GA to intervene with GAM has been shown to reduce treatment‐related toxicity, falls, and polypharmacy as well as improving quality of life, communication, and advance care planning. Although the implementation of GAM across oncology settings remains challenging, the PGA may facilitate its use in routine cancer care settings. In addition, systematic engagement of the oncology workforce and integration of technology‐based approaches may enhance further penetration of GA/GAM in cancer care to improve outcomes of older patients and caregivers. Finally, it is essential to prioritize health equity in geriatric oncology research and explore how GAM may reduce inequities in cancer care delivery for underserved and marginalized populations.

Supplementary Material

ACKNOWLEDGMENTS

The authors thank Susan Rosenthal, MD, for editorial assistance and review of the article.

This work was supported by the National Institute on Aging (K76 AG064394 and R0I AG077053 [Allison Magnuson]; K01AG068592 [Melody K. Schiaffino]), the National Cancer Institute (K01CA276257; Nikeesha Gilmore), and the Robert A. Winn Diversity in Clinical Trials Award Program established by the Bristol Myers Squibb Foundation (Tanyanika Phillips).

This work was also supported by the National Cancer Institute (R00CA237744; Kah Poh Loh), the National Institute of Aging (R03AG073985; Kah Poh Loh), the Conquer Cancer Foundation American Society of Clinical Oncology‐Walther Cancer Foundation Career Development Award (Kah Poh Loh), the Patient‐Centered Outcomes Research Institute (DI‐2020C3‐21003; Lisa M. Lowenstein and Supriya Mohile), the American Cancer Society (MRSG‐18‐225‐01‐CPPB; Lisa A. Lowenstein), the National Institute on Aging (R33 AG059206; Supriya Mohile, William Dale, and Heidi D. Klepin), and the National Institute on Aging (K24AG056589; Supriya Mohile).

Funding information

National Institute on Aging, Grant/Award Numbers: K76 AG064394, R0I AG077053, K01AG068592, R03AG073985, R33 AG059206, K24AG056589; National Cancer Institute, Grant/Award Numbers: K01CA276257, R00CA237744; Bristol Myers Squibb Foundation; Conquer Cancer Foundation American Society of Clinical Oncology‐Walther Cancer Foundation Career Development Award; Patient‐Centered Outcomes Research Institute, Grant/Award Number: DI‐2020C3‐21003; American Cancer Society, Grant/Award Number: MRSG‐18‐225‐01‐CPPB

SUPPORTING INFORMATION

Additional supporting information can be found online in the Supporting Information section at the end of this article.

CONFLICT OF INTEREST STATEMENT

Melody K. Schiaffino owns stock in Moderna and AstraZeneca. Grant R. Williams reports personal/consulting fees from Takeda Oncology outside the submitted work. The remaining authors disclosed no conflicts of interest.

REFERENCES

1. Oken MM , Creech RH , Tormey DC , Toxicity and response criteria of the Eastern Cooperative Oncology Group . Am J Clin Oncol . 1982 ; 5 ( 6 ): 649 – 656 . doi: 10.1097/00000421-198212000-00014 7165009

2. Karnofsky DA , Burchenal JH . The clinical evaluation of chemotherapeutic agents in cancer . In: MacLeod CM , ed. Evaluation of Chemotherapeutic Agents . Columbia University Press ; 1949 : 191 – 205 .

3. Hurria A , Togawa K , Mohile SG , Predicting chemotherapy toxicity in older adults with cancer: a prospective multicenter study . J Clin Oncol . 2011 ; 29 ( 25 ): 3457 – 3465 . doi: 10.1200/JCO.2011.34.7625 21810685 PMC3624700

4. Taylor AE , Olver IN , Sivanthan T , Chi M , Purnell C . Observer error in grading performance status in cancer patients . Support Care Cancer . 1999 ; 7 ( 5 ): 332 – 335 . doi: 10.1007/s005200050271 10483818

5. Kelly CM , Shahrokni A . Moving beyond Karnofsky and ECOG performance status assessments with new technologies . J Oncol . 2016 ; 2016 : 1 – 13 . doi: 10.1155/2016/6186543 PMC4811104 27066075

6. Jolly TA , Deal AM , Nyrop KA , Geriatric assessment‐identified deficits in older cancer patients with normal performance status . Oncologist . 2015 ; 20 ( 4 ): 379 – 385 . doi: 10.1634/theoncologist.2014-0247 25765876 PMC4391761

7. Broderick JM , Hussey J , Kennedy MJ , O’ Donnell DM . Patients over 65 years are assigned lower ECOG PS scores than younger patients, although objectively measured physical activity is no different . J Geriatr Oncol . 2014 ; 5 ( 1 ): 49 – 56 . doi: 10.1016/j.jgo.2013.07.010 24484718

8. Magnuson A , Bruinooge SS , Singh H , Modernizing clinical trial eligibility criteria: recommendations of the ASCO–Friends of Cancer Research Performance Status Work Group . Clin Cancer Res . 2021 ; 27 ( 9 ): 2424 – 2429 . doi: 10.1158/1078-0432.CCR-20-3868 33563633 PMC8102305

9. Hurria A , Gupta S , Zauderer M , Developing a cancer‐specific geriatric assessment: a feasibility study . Cancer . 2005 ; 104 ( 9 ): 1998 – 2005 . doi: 10.1002/cncr.21422 16206252

10. Dale W , Klepin HD , Williams GR , Practical assessment and management of vulnerabilities in older patients receiving systemic cancer therapy: ASCO guideline update . J Clin Oncol . 2023 ; 41 ( 26 ): 4293 – 4312 . doi: 10.1200/jco.23.00933 37459573 PMC12803700

11. Wildiers H , Heeren P , Puts M , International Society of Geriatric Oncology consensus on geriatric assessment in older patients with cancer . J Clin Oncol . 2014 ; 32 ( 24 ): 2595 – 2603 . doi: 10.1200/jco.2013.54.8347 25071125 PMC4876338

12. Biganzoli L , Battisti NML , Wildiers H , Updated recommendations regarding the management of older patients with breast cancer: a joint paper from the European Society of Breast Cancer Specialists (EUSOMA) and the International Society of Geriatric Oncology (SIOG) . Lancet Oncol . 2021 ; 22 ( 7 ): e327 – e340 . doi: 10.1016/s1470-2045(20)30741-5 34000244

13. Mottet N , Ribal MJ , Boyle H , Management of bladder cancer in older patients: position paper of an SIOG Task Force . J Geriatr Oncol . 2020 ; 11 ( 7 ): 1043 – 1053 . doi: 10.1016/j.jgo.2020.02.001 32057720

14. Kanesvaran R , Le Saux O , Motzer R , Elderly patients with metastatic renal cell carcinoma: position paper from the International Society of Geriatric Oncology . Lancet Oncol . 2018 ; 19 ( 6 ): e317 – e326 . doi: 10.1016/s1470-2045(18)30125-6 29893263

15. Extermann M , Artz A , Rebollo MA , Treating acute myelogenous leukemia in patients aged 70 and above: recommendations from the International Society of Geriatric Oncology (SIOG) . J Geriatr Oncol . 2024 ; 15 ( 2 ): 101626 . doi: 10.1016/j.jgo.2023.101626 37741771

16. Klepin HD , Neuendorff NR , Larson RA , Treatment of acute promyelocytic leukemia in older patients: recommendations of an International Society of Geriatric Oncology (SIOG) Task Force . J Geriatr Oncol . 2020 ; 11 ( 8 ): 1199 – 1209 . doi: 10.1016/j.jgo.2020.03.019 32273246

17. Stauder R , Eichhorst B , Hamaker ME , Management of chronic lymphocytic leukemia (CLL) in the elderly: a position paper from an international Society of Geriatric Oncology (SIOG) Task Force . Ann Oncol . 2017 ; 28 ( 2 ): 218 – 227 . doi: 10.1093/annonc/mdw547 27803007

18. Mohile SG , Dale W , Somerfield MR , Practical assessment and management of vulnerabilities in older patients receiving chemotherapy: ASCO guideline for geriatric oncology . J Clin Oncol . 2018 ; 36 ( 22 ): 2326 – 2347 . doi: 10.1200/JCO.2018.78.8687 29782209 PMC6063790

19. Dotan E , Walter LC , Browner IS , NCCN Guidelines® Insights: Older Adult Oncology, version 1.2021 . J Natl Compr Canc Netw . 2021 ; 19 ( 9 ): 1006 – 1019 . doi: 10.6004/jnccn.2021.0043 34551388

20. Dale W , Williams GR , Amy RM , How Is geriatric assessment used in clinical practice for older adults with cancer? A survey of cancer providers by the American Society of Clinical Oncology . JCO Oncol Pract . 2021 ; 17 ( 6 ): 336 – 344 . doi: 10.1200/op.20.00442 33064058 PMC8462667

21. Hurria A , Mohile S , Gajra A , Validation of a prediction tool for chemotherapy toxicity in older adults with cancer . J Clin Oncol . 2016 ; 34 ( 20 ): 2366 – 2371 . doi: 10.1200/JCO.2015.65.4327 27185838 PMC5321104

22. Mohamed MR , Loh KP , Mohile SG , External validation of risk factors for unplanned hospitalization in older adults with advanced cancer receiving chemotherapy . J Natl Compr Canc Netw . 2023 ; 21 ( 3 ): 273 – 280 .e3. doi: 10.6004/jnccn.2022.7094 36898361 PMC10966463

23. Wildes TM , Maggiore RJ , Tew WP , Factors associated with falls in older adults with cancer: a validated model from the Cancer and Aging Research Group . Support Care Cancer . 2018 ; 26 ( 10 ): 3563 – 3570 . doi: 10.1007/s00520-018-4212-3 29705872 PMC6117216

24. Pang A , Jiali L , Ng A , Use of the Cancer and Aging Research Group predictive model for chemotherapy‐related toxic effects in a multiethnic, older adult Asian population . JAMA Netw Open . 2022 ; 5 ( 10 ): e2237196 . doi: 10.1001/jamanetworkopen.2022.37196 PMC9579905 36255721

25. Suto H , Inui Y , Okamura A . Validity of the Cancer and Aging Research Group predictive tool in older Japanese patients . Cancers (Basel) . 2022 ; 14 ( 9 ) 2075 . doi: 10.3390/cancers14092075 35565205 PMC9104937

26. Alibhai SMH , Breunis H , Hansen AR , Examining the ability of the Cancer and Aging Research Group tool to predict toxicity in older men receiving chemotherapy or androgen‐receptor‐targeted therapy for metastatic castration‐resistant prostate cancer . Cancer . 2021 ; 127 ( 14 ): 2587 – 2594 . doi: 10.1002/cncr.33523 [ 33798267

27. Nishijima TF , Deal AM , Williams GR , Sanoff HK , Nyrop KA , Muss HB . Impact of the Cancer and Aging Research Group score and treatment intensity on survival and toxicity outcomes in older adults with advanced noncolorectal gastrointestinal cancers . Cancer . 2022 ; 128 ( 10 ): 1929 – 1936 . doi: 10.1002/cncr.34135 [ 35147991

28. Moth EB , Kiely BE , Stefanic N , Predicting chemotherapy toxicity in older adults: comparing the predictive value of the CARG Toxicity Score with oncologists’ estimates of toxicity based on clinical judgement . J Geriatr Oncol . 2019 ; 10 ( 2 ): 202 – 209 . doi: 10.1016/j.jgo.2018.08.010 [ 30224184

29. Magnuson A , Sedrak MS , Gross CP , Development and validation of a risk tool for predicting severe toxicity in older adults receiving chemotherapy for early‐stage breast cancer . J Clin Oncol . 2021 ; 39 ( 6 ): 608 – 618 . doi: 10.1200/JCO.20.02063 [ 33444080 PMC8189621

30. Sedrak MS , Sun CL , Ji J , Low‐intensity adjuvant chemotherapy for breast cancer in older women: results from the prospective multicenter HOPE trial . J Clin Oncol . 2023 ; 41 ( 2 ): 316 – 326 . doi: 10.1200/JCO.22.01440 [ 36455189 PMC9839299

31. Extermann M , Boler I , Reich RR , Predicting the risk of chemotherapy toxicity in older patients: the Chemotherapy Risk Assessment Scale for High‐Age Patients (CRASH) score . Cancer . 2012 ; 118 ( 13 ): 3377 – 3386 . doi: 10.1002/cncr.26646 [ 22072065

32. Rosko AE , Wall SA , Huang Y , Evaluating the CARG chemotherapy toxicity calculator among older adults newly diagnosed with hematologic malignancy [abstract] . Blood . 2021 ; 138 ( suppl 1 ): 1931 . doi: 10.1182/blood-2021-153850

33. Mariano C , Jamal R , Bains P , Utility of a chemotherapy toxicity prediction tool for older patients in a community setting . Curr Oncol . 2019 ; 26 ( 4 ): 234 – 239 . doi: 10.3747/co.26.4869 [ 31548802 PMC6726281

34. Ortland I , Mendel Ott M , Kowar M , Comparing the performance of the CARG and the CRASH score for predicting toxicity in older patients with cancer . J Geriatr Oncol . 2020 ; 11 ( 6 ): 997 – 1005 . doi: 10.1016/j.jgo.2019.12.016 [ 31928942

35. Klepin HD , Geiger AM , Tooze JA , Geriatric assessment predicts survival for older adults receiving induction chemotherapy for acute myelogenous leukemia . Blood . 2013 ; 121 ( 21 ): 4287 – 4294 . doi: 10.1182/blood-2012-12-471680 23550038 PMC3663423

36. Min GJ , Cho BS , Park SS , Geriatric assessment predicts nonfatal toxicities and survival for intensively treated older adults with AML . Blood . 2022 ; 139 ( 11 ): 1646 – 1658 . doi: 10.1182/blood.2021013671 35007323

37. Saad M , Loh KP , Tooze JA , Geriatric assessment and survival among older adults receiving postremission therapy for acute myeloid leukemia . Blood . 2020 ; 136 ( 23 ): 2715 – 2719 . doi: 10.1182/blood.2020005498 32698198 PMC7735162

38. Molga A , Wall M , Chhetri R , Comprehensive geriatric assessment predicts azacitidine treatment duration and survival in older patients with myelodysplastic syndromes . J Geriatr Oncol . 2020 ; 11 ( 1 ): 114 – 120 . doi: 10.1016/j.jgo.2019.02.002 31023599

39. Evens AM , Advani RH , Helenowski IB , Multicenter phase II study of sequential brentuximab vedotin and doxorubicin, vinblastine, and dacarbazine chemotherapy for older patients with untreated classical Hodgkin lymphoma . J Clin Oncol . 2018 ; 36 ( 30 ): 3015 – 3022 . doi: 10.1200/JCO.2018.79.0139 30179569

40. Nabhan C , Smith SM , Helenowski I , Analysis of very elderly (≥80 years) non‐Hodgkin lymphoma: impact of functional status and co‐morbidities on outcome . Br J Haematol . 2012 ; 156 ( 2 ): 196 – 204 . doi: 10.1111/j.1365-2141.2011.08934.x 22084970

41. Tucci A , Martelli M , Rigacci L , Comprehensive geriatric assessment is an essential tool to support treatment decisions in elderly patients with diffuse large B‐cell lymphoma: a prospective multicenter evaluation in 173 patients by the Lymphoma Italian Foundation (FIL) . Leuk Lymphoma . 2015 ; 56 ( 4 ): 921 – 926 . doi: 10.3109/10428194.2014.953142 25110825

42. Johnson PC , Woyach JA , Ulrich A , Geriatric assessment measures are predictive of outcomes in chronic lymphocytic leukemia . J Geriatr Oncol . 2023 ; 14 ( 6 ): 101538 . doi: 10.1016/j.jgo.2023.101538 PMC10599966 37329769

43. Palumbo A , Bringhen S , Mateos MV , Geriatric assessment predicts survival and toxicities in elderly myeloma patients: an International Myeloma Working Group report . Blood . 2015 ; 125 ( 13 ): 2068 – 2074 . doi: 10.1182/blood-2014-12-615187 25628469 PMC4375104

44. Olin RL , Fretham C , Pasquini MC , Geriatric assessment in older alloHCT recipients: association of functional and cognitive impairment with outcomes . Blood Adv . 2020 ; 4 ( 12 ): 2810 – 2820 . doi: 10.1182/bloodadvances.2020001719 32574365 PMC7322958

45. Muffly LS , Kocherginsky M , Stock W , Geriatric assessment to predict survival in older allogeneic hematopoietic cell transplantation recipients . Haematologica . 2014 ; 99 ( 8 ): 1373 – 1379 . doi: 10.3324/haematol.2014.103655 24816237 PMC4116837

46. Sorror ML , Storer BE , Nyland J , Estey EH . Revised acute myeloid leukemia composite model using the 2017 European LeukemiaNet Risk classification . JAMA Oncol . 2019 ; 5 ( 7 ): 1062 . doi: 10.1001/jamaoncol.2019.0902 31095246 PMC6537840

47. Sorror ML , Storer BE , Fathi AT , Development and validation of a novel acute myeloid leukemia–composite model to estimate risks of mortality . JAMA Oncol . 2017 ; 3 ( 12 ): 1675 . doi: 10.1001/jamaoncol.2017.2714 28880971 PMC5824273

48. Wan BA , Nazha A , Starkman R , Revised 15‐item MDS‐specific frailty scale maintains prognostic potential . Leukemia . 2020 ; 34 ( 12 ): 3434 – 3438 . doi: 10.1038/s41375-020-01026-y 32855438

49. Mozessohn L , Li Q , Liu N , Impact of frailty on health care resource utilization and costs of care in myelodysplastic syndromes . JCO Oncol Pract . 2023 ; 19 ( 4 ): e559 – e569 . doi: 10.1200/OP.22.00668 36763927 PMC10101507

50. Starkman R , Alibhai S , Wells RA , An MDS‐specific frailty index based on cumulative deficits adds independent prognostic information to clinical prognostic scoring . Leukemia . 2020 ; 34 ( 5 ): 1394 – 1406 . doi: 10.1038/s41375-019-0666-7 31811236

51. Engelhardt M , Domm AS , Dold SM , A concise revised Myeloma Comorbidity Index as a valid prognostic instrument in a large cohort of 801 multiple myeloma patients . Haematologica . 2017 ; 102 ( 5 ): 910 – 921 . doi: 10.3324/haematol.2016.162693 [ 28154088 PMC5477610

52. Facon T , Dimopoulos MA , Meuleman N , A simplified frailty scale predicts outcomes in transplant‐ineligible patients with newly diagnosed multiple myeloma treated in the FIRST (MM‐020) trial . Leukemia . 2020 ; 34 ( 1 ): 224 – 233 . doi: 10.1038/s41375-019-0539-0 31427722 PMC7214253

53. Merli F , Luminari S , Tucci A , Simplified geriatric assessment in older patients with diffuse large B‐cell lymphoma: the Prospective Elderly Project of the Fondazione Italiana Linfomi . J Clin Oncol . 2021 ; 39 ( 11 ): 1214 – 1222 . doi: 10.1200/JCO.20.02465 33577377

54. Oiwa K , Fujita K , Lee S , Utility of the Geriatric 8 for the prediction of therapy‐related toxicity in older adults with diffuse large B‐cell lymphoma . Oncologist . 2021 ; 26 ( 3 ): 215 – 223 . doi: 10.1002/onco.13641 33320984 PMC7930418

55. Lee S , Fujita K , Morishita T , Association of the Geriatric 8 with treatment intensity and prognosis in older patients with diffuse large B‐cell lymphoma . Br J Haematol . 2021 ; 194 ( 2 ): 325 – 335 . doi: 10.1111/bjh.17554 34041751

56. Miura K , Konishi J , Miyake T , A host‐dependent prognostic model for elderly patients with diffuse large B‐cell lymphoma . Oncologist . 2017 ; 22 ( 5 ): 554 – 560 . doi: 10.1634/theoncologist.2016-0260 28408622 PMC5423505

57. Sorror ML , Maris MB , Storb R , Hematopoietic cell transplantation (HCT)‐specific comorbidity index: a new tool for risk assessment before allogeneic HCT . Blood . 2005 ; 106 ( 8 ): 2912 – 2919 . doi: 10.1182/blood-2005-05-2004 15994282 PMC1895304

58. De La Rubia J , González B , Cruz‐Jentoft AJ , Geriatric assessment in hematology scale predicts treatment tolerability in older patients diagnosed with hematological malignancies: the RETROGAH study . J Geriatr Oncol 2023 ; 14 ( 1 ): 101401 . doi: 10.1016/j.jgo.2022.10.016 36404260

59. Giri S , Al‐Obaidi M , Harmon C , Patient‐reported geriatric assessment‐based frailty index among older adults with gastrointestinal malignancies . J Am Geriatr Soc . 2023 ; 71 ( 1 ): 136 – 144 . doi: 10.1111/jgs.18054 36208421 PMC9870847

60. Artz A , Logan BR , Saber W , The Composite Health Risk Assessment Model (CHARM) to predict 1‐year non‐relapse mortality (NRM) among older recipients of allogeneic transplantation: a prospective BMT‐CTN study 1704 [abstract] . Blood . 2023 ; 142 ( suppl 1 ): 109 . doi: 10.1182/blood-2023-173855

61. Hamaker M , Lund C , Te Molder M , Geriatric assessment in the management of older patients with cancer—a systematic review (update) . J Geriatr Oncol . 2022 ; 13 ( 6 ): 761 – 777 . doi: 10.1016/j.jgo.2022.04.008 [ 35545495

62. Corre R , Greillier L , Le Caër H , Use of a comprehensive geriatric assessment for the management of elderly patients with advanced non–small‐cell lung cancer: the phase III randomized ESOGIA‐GFPC‐GECP 08‐02 study . J Clin Oncol . 2016 ; 34 ( 13 ): 1476 – 1483 . doi: 10.1200/JCO.2015.63.5839 [ 26884557

63. Merli F , Luminari S , Rossi G , Cyclophosphamide, doxorubicin, vincristine, prednisone and rituximab versus epirubicin, cyclophosphamide, vinblastine, prednisone and rituximab for the initial treatment of elderly “fit” patients with diffuse large B‐cell lymphoma: results from the ANZINTER3 trial of the Intergruppo Italiano Linfomi . Leuk Lymphoma . 2012 ; 53 ( 4 ): 581 – 588 . doi: 10.3109/10428194.2011.621565 [ 21895543

64. Bhatt VR , Wichman C , Al‐Kadhimi ZS , Integrating geriatric assessment and genetic profiling to personalize therapy selection in older adults with acute myeloid leukemia . J Geriatr Oncol . 2022 ; 13 ( 6 ): 871 – 874 . doi: 10.1016/j.jgo.2022.04.005 [ 35450817 PMC9482687

65. Dotan E , Catalano P , Lenchik L , The GIANT trial (ECOG‐ACRIN EA2186) methods paper: a randomized phase II study of gemcitabine and nab‐paclitaxel compared with 5‐fluorouracil, leucovorin, and liposomal irinotecan in older patients with treatment‐naïve metastatic pancreatic cancer—defining a new treatment option for older vulnerable patients . J Geriatr Oncol . 2023 ; 14 ( 3 ): 101474 . doi: 10.1016/j.jgo.2023.101474 [ PMC10425127 36963200

66. Magnuson A , Van der Walde N , McKoy JM , Integrating geriatric assessment measures into National Cancer Institute clinical trials . J Natl Cancer Inst Monogr . 2022 ; 2022 ( 60 ): 142 – 150 . doi: 10.1093/jncimonographs/lgac021 [ 36519816 PMC9949568

67. Fried TR , Bradley EH , Towle VR , Allore H . Understanding the treatment preferences of seriously ill patients . N Engl J Med . 2002 ; 346 ( 14 ): 1061 . doi: 10.1056/NEJMsa012528 [ 11932474

68. Loh KP , Mohile SG , Epstein RM , Willingness to bear adversity and beliefs about the curability of advanced cancer in older adults . Cancer . 2019 ; 125 ( 14 ): 2506 – 2513 . doi: 10.1002/cncr.32074 [ 30920646 PMC6602839

69. Soto‐Perez‐de‐Celis E , Dale W , Katheria V , Outcome prioritization and preferences among older adults with cancer starting chemotherapy in a randomized clinical trial . Cancer . 2024 ; 130 : 3000 – 3010 . doi: 10.1002/cncr.35333 [ 38630903 PMC11863993

70. Anwar MR , Yeretzian ST , Ayala AP , Effectiveness of geriatric assessment and management in older cancer patients: a systematic review and meta‐analysis . J Natl Cancer Inst . 2023 ; 115 ( 12 ): 1483 – 1496 . doi: 10.1093/jnci/djad200 [ 37738290

71. Li D , Sun CL , Kim H , Geriatric Assessment–Driven Intervention (GAIN) on chemotherapy‐related toxic effects in older adults with cancer: a randomized clinical trial . JAMA Oncol . 2021 ; 7 ( 11 ): e214158 . doi: 10.1001/jamaoncol.2021.4158 [ PMC8485211 34591080

72. Lund CM , Vistisen KK , Olsen AP , The effect of geriatric intervention in frail older patients receiving chemotherapy for colorectal cancer: a randomised trial (GERICO) . Br J Cancer . 2021 ; 124 ( 12 ): 1949 – 1958 . doi: 10.1038/s41416-021-01367-0 [ 33828260 PMC8185087

73. Soo WK , King MT , Pope A , Parente P , Dārziņš P , Davis ID . Integrated Geriatric Assessment and Treatment Effectiveness (INTEGERATE) in older people with cancer starting systemic anticancer treatment in Australia: a multicentre, open‐label, randomised controlled trial . Lancet Healthy Longev . 2022 ; 3 ( 9 ): e617 – e627 . doi: 10.1016/S2666-7568(22)00169-6 36102776

74. Ørum M , Eriksen SV , Gregersen M , The impact of a tailored follow‐up intervention on comprehensive geriatric assessment in older patients with cancer—a randomised controlled trial . J Geriatr Oncol . 2021 ; 12 ( 1 ): 41 – 48 . doi: 10.1016/j.jgo.2020.07.011 32747208

75. Puts M , Alqurini N , Strohschein F , Impact of geriatric assessment and management on quality of life, unplanned hospitalizations, toxicity, and survival for older adults with cancer: the randomized 5C trial . J Clin Oncol . 2023 ; 41 ( 4 ): 847 – 858 . doi: 10.1200/jco.22.01007 36473126 PMC9902020

76. Paillaud E , Brugel L , Bertolus C , Effectiveness of geriatric assessment‐driven interventions on survival and functional and nutritional status in older patients with head and neck cancer: a randomized controlled trial (EGeSOR) . Cancers (Basel) . 2022 ; 14 ( 13 ): 3290 . doi: 10.3390/cancers14133290 35805060 PMC9265581

77. Mohile SG , Mohamed MR , Xu H , Evaluation of geriatric assessment and management on the toxic effects of cancer treatment (GAP70+): a cluster‐randomised study . Lancet . 2021 ; 398 ( 10314 ): 1894 – 1904 . doi: 10.1016/S0140-6736(21)01789-X 34741815 PMC8647163

78. Mohile SG , Epstein RM , Hurria A , Communication with older patients with cancer using geriatric assessment: a cluster‐randomized clinical trial from the National Cancer Institute Community Oncology Research Program . JAMA Oncol . 2020 ; 6 ( 2 ): 196 . doi: 10.1001/jamaoncol.2019.4728 31697365 PMC6865234

79. DuMontier C , Uno H , Hshieh T , Randomized controlled trial of geriatric consultation versus standard care in older adults with hematologic malignancies . Haematologica . 2022 ; 107 ( 5 ): 1172 – 1180 . doi: 10.3324/haematol.2021.278802 34551505 PMC9052912

80. Culakova E , Mohile SG , Peppone L , Effects of a geriatric assessment intervention on patient‐reported symptomatic toxicity in older adults with advanced cancer . J Clin Oncol . 2023 ; 41 ( 4 ): 835 – 846 . doi: 10.1200/JCO.22.00738 36356279 PMC9901996

81. Mohamed MR , Kyi K , Mohile SG , Prevalence of and factors associated with treatment modification at first cycle in older adults with advanced cancer receiving palliative treatment . J Geriatr Oncol . 2021 ; 12 ( 8 ): 1208 – 1213 . doi: 10.1016/j.jgo.2021.06.007 34272204 PMC8557119

82. Gajra A , Jeune‐Smith Y , Fortier S , The use and knowledge of validated geriatric assessment instruments among US community oncologists . JCO Oncol Pract . 2022 ; 18 ( 7 ): e1081 – e1090 . doi: 10.1200/op.21.00743 35263162

83. Mohile SG , Velarde C , Hurria A , Geriatric assessment‐guided care processes for older adults: a Delphi consensus of geriatric oncology experts . J Natl Comp Canc Netw . 2015 ; 13 ( 9 ): 1120 – 1130 . doi: 10.6004/jnccn.2015.0137 PMC4630807 26358796

84. DuMontier C , Loh KP , Bain PA , Defining undertreatment and overtreatment in older adults with cancer: a scoping literature review . J Clin Oncol . 2020 ; 38 ( 22 ): 2558 – 2569 . doi: 10.1200/jco.19.02809 [ 32250717 PMC7392742

85. Williams GR , Hopkins JO , Klepin HD , Practical assessment and management of vulnerabilities in older patients receiving systemic cancer therapy: ASCO guideline questions and answers . JCO Oncol Pract . 2023 ; 19 ( 9 ): 718 – 723 . doi: 10.1200/op.23.00263 [ 37459585

86. Plotkin E , Dotan E , Nightingale G . Growing need demands new approaches to caring for older adults with cancer . Oncol Issues . 2019 ; 34 ( 5 ): 62 – 67 .

87. Williams GR , Weaver KE , Lesser GJ , Capacity to provide geriatric specialty care for older adults in community oncology practices . Oncologist . 2020 ; 25 ( 12 ): 1032 – 1038 . doi: 10.1634/theoncologist.2020-0189 [ 32820842 PMC7938409

88. Verduzco‐Aguirre HC , Bolaño Guerra LM , Culakova E , Barriers and facilitators for the implementation of geriatric oncology principles in Mexico: a mixed‐methods study . JCO Glob Oncol . 2022 ; 8 :e2100390. doi: 10.1200/go.21.00390 PMC9005260 35353596

89. Swartz K , Chapman A , Zhan T , Wen KY . Process evaluation of a G8 screening tool implementation in an outpatient oncology center . J Geriatr Oncol . 2024 ; 15 ( 1 ): 101605 . doi: 10.1016/j.jgo.2023.101605 PMC10843632 37633778

90. Klepin HD , Geiger AM , Tooze JA , The feasibility of inpatient geriatric assessment for older adults receiving induction chemotherapy for acute myelogenous leukemia . J Am Geriatr Soc . 2011 ; 59 ( 10 ): 1837 – 1846 . doi: 10.1111/j.1532-5415.2011.03614.x 22091497 PMC3782375

91. Ritchie EK , Klepin HD , Storrick E , Geriatric assessment for older adults receiving less‐intensive therapy for acute myeloid leukemia: report of CALGB 361101 . Blood Adv . 2022 ; 6 ( 12 ): 3812 – 3820 . doi: 10.1182/bloodadvances.2021006872 35420672 PMC9631575

92. Klepin HD , Ritchie E , Major‐Elechi B , Geriatric assessment among older adults receiving intensive therapy for acute myeloid leukemia: report of CALGB 361006 (Alliance) . J Geriatr Oncol . 2020 ; 11 ( 1 ): 107 – 113 . doi: 10.1016/j.jgo.2019.10.002 31668825 PMC6943189

93. Williams GR , Deal AM , Jolly TA , Feasibility of geriatric assessment in community oncology clinics . J Geriatr Oncol . 2014 ; 5 ( 3 ): 245 – 251 . doi: 10.1016/j.jgo.2014.03.001 24703978

94. Hurria A , Cirrincione CT , Muss HB , Implementing a geriatric assessment in cooperative group clinical cancer trials: CALGB 360401 . J Clin Oncol . 2011 ; 29 ( 10 ): 1290 – 1296 . doi: 10.1200/JCO.2010.30.6985 21357782 PMC3083997

95. Bellera CA , Rainfray M , Mathoulin‐Pélissier S , Screening older cancer patients: first evaluation of the G‐8 geriatric screening tool . Ann Oncol . 2012 ; 23 ( 8 ): 2166 – 2172 . doi: 10.1093/annonc/mdr587 22250183

96. Saliba D , Elliott M , Rubenstein LZ , The Vulnerable Elders Survey: a tool for identifying vulnerable older people in the community . J Am Geriatr Soc . 2001 ; 49 ( 12 ): 1691 – 1699 . doi: 10.1046/j.1532-5415.2001.49281.x 11844005

97. Garcia MV , Agar MR , Soo WK , To T , Phillips JL . Screening tools for identifying older adults with cancer who may benefit from a geriatric assessment: a systematic review . JAMA Oncol . 2021 ; 7 ( 4 ): 616 . doi: 10.1001/jamaoncol.2020.6736 33443547

98. Van Walree IC , Vondeling AM , Vink GR , Development of a self‐reported version of the G8 screening tool . J Geriatr Oncol . 2019 ; 10 ( 6 ): 926 – 930 . doi: 10.1016/j.jgo.2019.08.011 31477512

99. Soubeyran P , Bellera C , Goyard J , Screening for vulnerability in older cancer patients: the ONCODAGE prospective multicenter cohort study . PLoS One . 2014 ; 9 ( 12 ): e115060 . doi: 10.1371/journal.pone.0115060 PMC4263738 25503576

100. Chakiba C , Bellera C , Etchepare F , Mathoulin‐Pelissier S , Rainfray M , Soubeyran P . The prognostic value of G8 for functional decline . J Geriatr Oncol . 2019 ; 10 ( 6 ): 921 – 925 . doi: 10.1016/j.jgo.2018.12.004 30638869

101. Banna GL , Basso U , Giunta EF , The Geriatric G8 score is associated with survival outcomes in older patients with advanced prostate cancer in the ADHERE prospective study of the Meet‐URO Network . Curr Oncol . 2022 ; 29 ( 10 ): 7745 – 7753 . doi: 10.3390/curroncol29100612 36290889 PMC9600362

102. González Serrano A , Laurent M , Barnay T , A two‐step frailty assessment strategy in older patients with solid tumors: a decision curve analysis . J Clin Oncol . 2023 ; 41 ( 4 ): 826 – 834 . doi: 10.1200/jco.22.01118 36306481 PMC9901978

103. Mac Eochagain C , Barrell A , Slavova‐Boneva V , Implementation of a geriatric oncology service at the Royal Marsden Hospital . J Geriatr Oncol . 2024 ; 15 ( 2 ): 101698 . doi: 10.1016/j.jgo.2023.101698 38219333

104. Vinod S , Khoo A , Berry M , Implementation and evaluation of a geriatric‐oncology model of care for older adults with lung cancer . J Geriatr Oncol . 2023 ; 14 ( 8 ): 101578 . doi: 10.1016/j.jgo.2023.101578 37422350

105. de Barros LPL , de Oliveira Muniz Koch L , de Oliveira Lima JT , Development of geriatric oncology in Latin America: a report from the Latin American Cooperative Oncology Group . J Geriatr Oncol . 2024 ; 15 ( 3 ): 101642 . doi: 10.1016/j.jgo.2023.101642 37977899

106. Michie S , van Stralen MM , West R . The behaviour change wheel: a new method for characterising and designing behaviour change interventions . Implement Sci . 2011 ; 6 ( 1 ): 42 . doi: 10.1186/1748-5908-6-42 21513547 PMC3096582

107. Harmon C , Fowler M , Giri S , Implementation of the Web‐Enabled Cancer & Aging Resilience Evaluation (WeCARE) in an outpatient oncology setting . J Geriatr Oncol . 2023 ; 14 ( 8 ): 101644 . doi: 10.1016/j.jgo.2023.101644 PMC10895518 37806291

108. Rosko AE , Steer C , Chien LC , The Cancer and Aging Research Group (CARG) infrastructure: the clinical implementation core . J Geriatr Oncol . 2021 ; 12 ( 8 ): 1164 – 1165 . doi: 10.1016/j.jgo.2021.04.001 33875397 PMC8802293

109. Sedrak MS , Freedman RA , Cohen HJ , Older adult participation in cancer clinical trials: a systematic review of barriers and interventions . CA Cancer J Clin . 2021 ; 71 ( 1 ): 78 – 92 . doi: 10.3322/caac.21638 33002206 PMC7854940

110. Hurria A , Akiba C , Kim J , Reliability, validity, and feasibility of a computer‐based geriatric assessment for older adults with cancer . J Oncol Pract . 2016 ; 12 ( 12 ): e1025 – e1034 . doi: 10.1200/JOP.2016.013136 27624950 PMC5455588

111. Ball C , Francis J , Huang KT , Kadylak T , Cotten SR , Rikard RV . The physical–digital divide: exploring the social gap between digital natives and physical natives . J Appl Gerontol . 2019 ; 38 ( 8 ): 1167 – 1184 . doi: 10.1177/0733464817732518 29165009

112. Li W , Ornstein K , Li Y , Liu B . Technology use among cancer patients pre‐ and post‐COVID‐19 pandemic: the role of dementia . Innov Aging . 2021 ; 5 ( suppl ): 688 . doi: 10.1093/geroni/igab046.2584

113. Pew Research Center . Mobile Fact Sheet . Pew Research Center ; 2021 . Accessed January 21, 2024 . https://www.pewresearch.org/internet/fact‐sheet/mobile/

114. Pew Research Center . Internet, Broadband Fact Sheet . Pew Research Center ; 2021 . Accessed January 21, 2024 . https://www.pewresearch.org/internet/fact‐sheet/internet‐broadband/

115. Anthony D , Singer D , Kirch M , Use and Experiences with Patient Portals Among Older Adults . University of Michigan National Poll on Healthy Aging ; 2023 . Accessed January 21, 2024 . https://www.healthyagingpoll.org/reports‐more/report/use‐and‐experiences‐patient‐portals‐among‐older‐adults

116. Lee P , Aikens J , Richardson C , Mobile Health App Use Among Older Adults . University of Michigan National Poll on Healthy Aging ; 2022 . Accessed January 21, 2024 . https://www.healthyagingpoll.org/reports‐more/report/mobile‐health‐app‐use‐among‐older‐adults

117. Cook S , Munteanu C , Papadopoulos E , The development of an electronic geriatric assessment tool: Comprehensive Health Assessment for My Plan (CHAMP) . J Geriatr Oncol . 2023 ; 14 ( 1 ): 101384 . doi: 10.1016/j.jgo.2022.09.013 36216760

118. VanderWalde NA , Williams GR . Developing an electronic geriatric assessment to improve care of older adults with cancer receiving radiotherapy . Tech Innov Patient Support Radiat Oncol . 2020 ; 16 : 24 – 29 . doi: 10.1016/j.tipsro.2020.09.002 33385071 PMC7769846

119. Shahrokni A , Tin A , Downey RJ , Electronic rapid fitness assessment: a novel tool for preoperative evaluation of the geriatric oncology patient . J Natl Compr Canc Netw . 2017 ; 15 ( 2 ): 172 – 179 . doi: 10.6004/jnccn.2017.0018 28188187 PMC5507335

120. LoCastro M , Sanapala C , Wang Y , Patient‐centered communication tool for older patients with acute myeloid leukemia, their caregivers, and oncologists: a single‐arm pilot study . Cancer Med . 2023 ; 12 ( 7 ): 8581 – 8593 . doi: 10.1002/cam4.5547 36533397 PMC10134384

121. Loh KP , McHugh C , Mohile SG , Using information technology in the assessment and monitoring of geriatric oncology patients . Curr Oncol Rep . 2018 ; 20 ( 3 ): 25 . doi: 10.1007/s11912-018-0672-3 29511850 PMC5878089

122. DiGiovanni G , Mousaw K , Lloyd T , Development of a tele-health geriatric assessment model in response to the COVID‐19 pandemic . J Geriatr Oncol . 2020 ; 11 ( 5 ): 761 – 763 . doi: 10.1016/j.jgo.2020.04.007 32327321 PMC7164886

123. Bergerot CD , Bergerot PG , Razavi M , Implementation and evaluation of a remote geriatric assessment and intervention program in Brazil . Cancer . 2023 ; 129 ( 13 ): 2095 – 2102 . doi: 10.1002/cncr.34759 36964938

124. Wall SA , Knauss B , Compston A , Multidisciplinary telemedicine and the importance of being seen . J Geriatr Oncol . 2020 ; 11 ( 8 ): 1349 – 1351 . doi: 10.1016/j.jgo.2020.05.006 32482554 PMC7260477

125. Loh KP , Wang Y , Yilmaz S , Information technology and telemedicine services in community oncology practices . JCO Clin Cancer Inform . 2023 ; 7 :e2300086. doi: 10.1200/cci.23.00086 PMC10569779 37540817

126. Chien L , Roberts E , Soto‐Perez‐de‐Celis E , Telehealth in geriatric oncology: a novel approach to deliver multidisciplinary care for older adults with cancer . J Geriatr Oncol . 2020 ; 11 ( 2 ): 197 – 199 . doi: 10.1016/j.jgo.2019.06.011 31272897 PMC6938565

127. Alexander K , Hamlin PA , Tew WP , Development and implementation of an interdisciplinary telemedicine clinic for older patients with cancer—preliminary data . J Am Geriatr Soc . 2023 ; 71 ( 5 ): 1638 – 1649 . doi: 10.1111/jgs.18267 36744590 PMC10175129

128. Sanapala C , Jensen‐Battaglia M , Watson EE , In‐person and virtual assessment of short physical performance battery test in older adults with myeloid malignancies . Blood Adv . 2023 ; 7 ( 16 ): 4414 – 4417 . doi: 10.1182/bloodadvances.2022009396 36790922 PMC10440456

129. Piraux E , Caty G , Reychler G , Forget P , Deswysen Y . Feasibility and preliminary effectiveness of a tele‐prehabilitation program in esophagogastric cancer patients . J Clin Med . 2020 ; 9 ( 7 ): 2176 . doi: 10.3390/jcm9072176 32660126 PMC7408844

130. Chen M , Mohd Said N , Mohd Rais NC , Remaining agile in the COVID‐19 pandemic healthcare landscape—how we adopted a hybrid telemedicine geriatric oncology care model in an academic tertiary cancer center . J Geriatr Oncol . 2022 ; 13 ( 6 ): 856 – 861 . doi: 10.1016/j.jgo.2022.04.006 35461791 PMC9005364

131. Rocque G , Wheeler S , Williams GR . The missing voice in multidisciplinary tumor boards . J Geriatr Oncol . 2021 ; 12 ( 8 ): 1157 – 1158 . doi: 10.1016/j.jgo.2021.03.004 33722503 PMC8435048

132. Loh KP , Ramsdale E , Culakova E , Novel mHealth app to deliver geriatric assessment‐driven interventions for older adults with cancer: pilot feasibility and usability study . JMIR Cancer . 2018 ; 4 ( 2 ): e10296 . doi: 10.2196/10296 PMC6234352 30373733

133. Soto‐Perez‐De‐Celis E , Kim H , Rojo‐Castillo MP , A pilot study of an accelerometer‐equipped smartphone to monitor older adults with cancer receiving chemotherapy in Mexico . J Geriatr Oncol . 2018 ; 9 ( 2 ): 145 – 151 . doi: 10.1016/j.jgo.2017.09.008 29017891

134. Feng G , Parthipan M , Breunis H , Daily physical activity monitoring in older adults with metastatic prostate cancer on active treatment: feasibility and associations with toxicity . J Geriatr Oncol . 2023 ; 14 ( 7 ): 101576 . doi: 10.1016/j.jgo.2023.101576 37421787

135. Loh KP , Sanapala C , Watson EE , A single‐arm pilot study of a mobile health exercise intervention (GO‐EXCAP) in older patients with myeloid neoplasms . Blood Adv . 2022 ; 6 ( 13 ): 3850 – 3860 . doi: 10.1182/bloodadvances.2022007056 35320340 PMC9278283

136. Nipp RD , Horick NK , Deal AM , Differential effects of an electronic symptom monitoring intervention based on the age of patients with advanced cancer . Ann Oncol . 2020 ; 31 ( 1 ): 123 – 130 . doi: 10.1016/j.annonc.2019.09.003 31912785 PMC7497788

137. Qiao EM , Qian AS , Nalawade V , Evaluating high‐dimensional machine learning models to predict hospital mortality among older patients with cancer . JCO Clin Cancer Inform . 2022 ;( 6 ): e2100186 . doi: 10.1200/CCI.21.00186 PMC9225681 35671416

138. Ramsdale E , Kunduru M , Smith L , Supervised learning applied to classifying fallers versus non‐fallers among older adults with cancer . J Geriatr Oncol . 2023 ; 14 ( 4 ): 101498 . doi: 10.1016/j.jgo.2023.101498 PMC10174263 37084629

139. Venkatesh KP , Raza MM , Kvedar JC . Health digital twins as tools for precision medicine: considerations for computation, implementation, and regulation . NPJ Digit Med . 2022 ; 5 ( 1 ): 150 , doi: 10.1038/s41746-022-00694-7 36138125 PMC9500019

140. Wilkinson MD , Dumontier M , Aalbersberg IJ , The FAIR Guiding Principles for scientific data management and stewardship . Sci Data . 2016 ; 3 ( 1 ): 160018 . doi: 10.1038/sdata.2016.18 PMC4792175 26978244

141. 21st Century Cures Act: Interoperability, Information Blocking, and the ONC Health IT Certification Program. 85 Federal Register 25642 – 25961 . 2020 .

142. Herington J , McCradden MD , Creel K , Ethical considerations for artificial intelligence in medical imaging: data collection, development, and evaluation . J Nucl Med . 2023 ; 64 ( 12 ): 1848 – 1854 . doi: 10.2967/jnumed.123.266080 37827839 PMC10690124

143. Fox‐Grage W The Growing Racial and Ethnic Diversity of Older Adults . AARP Blogs ; March 7 , 2016 , Accessed January 21, 2024 . https://blog.aarp.org/thinking‐policy/the‐growing‐racial‐and‐ethnic‐diversity‐of‐older‐adults

144. Siegel RL , Giaquinto AN , Jemal A . Cancer statistics, 2024 . CA Cancer J Clin . 2024 ; 74 ( 1 ): 12 – 49 . doi: 10.3322/caac.21820 38230766

145. National Center for Health Statistics . Healthy People 2020 . Centers for Disease Control and Prevention ; 2021 .

146. Smith BD , Smith GL , Hurria A , Hortobagyi GN , Buchholz TA . Future of cancer incidence in the United States: burdens upon an aging, changing nation . J Clin Oncol . 2009 ; 27 ( 17 ): 2758 – 2765 . doi: 10.1200/JCO.2008.20.8983 19403886

147. Mandelblatt JS , Ruterbusch JJ , Thompson HS , Association between major discrimination and deficit accumulation in African American cancer survivors: the Detroit Research on Cancer Survivors study . Cancer . 2023 ; 129 ( 10 ): 1557 – 1568 . doi: 10.1002/cncr.34673 36935617 PMC10568940

148. Hastert TA , Kyko JM , Reed AR , Financial hardship and quality of life among African American and white cancer survivors: the role of limiting care due to cost . Cancer Epidemiol Biomarkers Prev . 2019 ; 28 ( 7 ): 1202 – 1211 . doi: 10.1158/1055-9965.EPI-18-1336 31061097 PMC6606374

149. Jones NL , Gilman SE , Cheng TL , Drury SS , Hill CV , Geronimus AT . Life course approaches to the causes of health disparities . Am J Public Health . 2019 ; 109 ( S1 ): S48 – S55 . doi: 10.2105/AJPH.2018.304738 30699022 PMC6356123

150. Braveman P , Gottlieb L The social determinants of health: it’s time to consider the causes of the causes . Public Health Rep . 2014 ; 129 ( 1 suppl 2 ): 19 – 31 . doi: 10.1177/00333549141291S206 PMC3863696 24385661

151. Dotan E , Lynch SM , Ryan JC , Mitchell EP . Disparities in care of older adults of color with cancer: a narrative review . Cancer Med . 2024 ; 13 ( 3 ): e6790 . doi: 10.1002/cam4.6790 38234214 PMC10905558

152. Williams GR , Fowler M , Giri S , Association of unmet basic resource needs with frailty and quality of life among older adults with cancer—results from the CARE registry . Cancer Med . 2023 ; 12 ( 12 ): 13846 – 13855 . doi: 10.1002/cam4.6038 37245226 PMC10315805

153. Williams GR , Al‐Obaidi M , Harmon C , Racial disparities in frailty and geriatric assessment impairments in older adults with cancer in the Deep South: results from the CARE registry . Cancer . 2022 ; 128 ( 12 ): 2313 – 2319 . doi: 10.1002/cncr.34178 35403211 PMC9437907

154. Zavala VA , Bracci PM , Carethers JM , Cancer health disparities in racial/ethnic minorities in the United States . Br J Cancer . 2021 ; 124 ( 2 ): 315 – 332 . doi: 10.1038/s41416-020-01038-6 32901135 PMC7852513

155. Sengupta R , Honey K . AACR Cancer Disparities Progress Report 2020: achieving the bold vision of health equity for racial and ethnic minorities and other underserved populations . Cancer Epidemiol Biomarkers Prev . 2020 ; 29 ( 10 ): 1843 . doi: 10.1158/1055-9965.EPI-20-0269 32938690

156. Phillips T , Sun C , Chien L , Geriatric Assessment‐Directed Supportive Care Intervention (GAIN‐S)‐implementation via telehealth in a lower‐resourced community [abstract] . 2024 ; 42 ( 16 suppl ): 1510 , doi: 10.1200/jco.2024.42.16_suppl.1510

157. Roth R , Barsi E . The Community Need Index. A new tool pinpoints health care disparities in communities throughout the nation . Health Prog . 2005 ; 86 ( 4 ): 32 – 38 . 16092512

158. Kind AJH , Buckingham WR . Making neighborhood‐disadvantage metrics accessible—The Neighborhood Atlas . N Engl J Med . 2018 ; 378 ( 26 ): 2456 – 2458 . doi: 10.1056/NEJMp1802313 29949490 PMC6051533

159. Flanagan BE , Gregory EW , Hallisey EJ , Heitgerd JL , Lewis B . A social vulnerability index for disaster management . J Homeland Secur Emerg Manage . 2011 ; 8 ( 1 ):Article 3. doi: 10.2202/1547-7355.1792

160. Ponce NA , Hays RD , Cunningham WE . Linguistic disparities in health care access and health status among older adults . J Gen Intern Med . 2006 ; 21 ( 7 ): 786 – 791 . doi: 10.1111/j.1525-1497.2006.00491.x 16808783 PMC1924691

161. Haldar S , Pillai D , Artiga S . Overview of Health Coverage and care for Individuals with Limited English Proficiency (LEP) . Kaiser Family Foundation ; 2023 . Accessed January 21, 2024 . https://www.kff.org/6c186f7/

162. Qian AS , Schiaffino MK , Nalawade V , Disparities in telemedicine during COVID‐19 . Cancer Med . 2022 ; 11 ( 4 ): 1192 – 1201 . doi: 10.1002/cam4.4518 34989148 PMC8855911

163. De B , Maroongroge S , Smith GL . Letter to the editor regarding “disparities in telemedicine during COVID‐19 .” Cancer Med . 2023 ; 12 ( 2 ): 1556 – 1557 . doi: 10.1002/cam4.5036 35837958 PMC9350141

164. Chen DW , Banerjee M , He X , Hidden disparities: how language influences patients’ access to cancer care . J Natl Compr Canc Netw . 2023 ; 21 ( 9 ): 951 – 959 .e1. doi: 10.6004/jnccn.2023.7037 37673110 PMC11033703

165. Schiaffino MK , Nara A , Mao L . Language services in hospitals vary by ownership and location . Health Affairs (Millwood) . 2016 ; 35 ( 8 ): 1399 – 1403 . doi: 10.1377/hlthaff.2015.0955 27503963

166. Leung B , Pilleron S , Bastiaannet E , Cancer treatment‐related decision‐making among culturally and linguistically diverse older adults with cancer: a scoping review by the International Society of Geriatric Oncology Nursing and Allied Health Interest Group . J Geriatr Oncol . 2023 ; 14 ( 8 ): 101607 . doi: 10.1016/j.jgo.2023.101607 37633779

167. Yilmaz S , Sanapala C , Schiaffino MK , Social justice and equity: why older adults with cancer belong—a life course perspective . Am Soc Clin Oncol Educ Book . 2022 ;( 42 ): 402 – 414 . doi: 10.1200/EDBK_349825 PMC11070065 35649203

168. Patel MI , Lopez AM , Blackstock W , Cancer disparities and health equity: a policy statement from the American Society of Clinical Oncology . J Clin Oncol . 2020 ; 38 ( 29 ): 3439 – 3448 . doi: 10.1200/JCO.20.00642 32783672 PMC7527158

169. Gilmore N , Grant SJ , Bethea TN , A scoping review of racial, ethnic, socioeconomic, and geographic disparities in the outcomes of older adults with cancer . J Am Geriatr Soc , 2024 ; 72 ( 6 ): 1867 – 1900 . doi: 10.1111/jgs.18881 38593225 PMC11187671

170. National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Health Care Services; Committee on Integrating Social Needs Care into the Delivery of Health Care to Improve the Nation’s Health . Integrating Social Care into the Delivery of Health Care: Moving Upstream to Improve The Nation’s Health . National Academies Press ; 2019 . 31940159

171. Tucker‐Seeley RD , Wallington SF , Canin B , Tang W , McKoy JM . Health equity for older adults with cancer . J Clin Oncol . 2021 ; 39 ( 19 ): 2205 – 2216 . doi: 10.1200/JCO.21.00207 34043411

172. Erikson C , Salsberg E , Forte G , Bruinooge S , Goldstein M . Future supply and demand for oncologists: challenges to assuring access to oncology services . J Oncol Pract . 2007 ; 3 ( 2 ): 79 – 86 . doi: 10.1200/JOP.0723601 20859376 PMC2793740

173. McKoy JM , Samaras AT , Bennett CL . Providing cancer care to a graying and diverse cancer population in the 21st century: are we prepared? J Clin Oncol . 2009 ; 27 ( 17 ): 2745 – 2746 . doi: 10.1200/JCO.2009.22.4352 19403884

174. Wallington SF , Brawley OW , Holmes MD . Socioeconomic status and breast cancer disparities . In: Koh HK , ed. Toward the Elimination of Cancer Disparities . Springer ; 2009 : 137 – 160 .

175. Committee on Family Caregiving for Older Adults; Board on Health Care Services; Health and Medicine Division; National Academies of Sciences, Engineering, and Medicine ; Schulz R , Eden J , eds. Families Caring for an Aging America . National Academies Press ; 2016 . 27905704

176. Hsu T , Loscalzo M , Ramani R , Factors associated with high burden in caregivers of older adults with cancer . Cancer . 2014 ; 120 ( 18 ): 2927 – 2935 . doi: 10.1002/cncr.28765 24898093 PMC4159406

177. Mollica MA , Litzelman K , Rowland JH , Kent EE . The role of medical/nursing skills training in caregiver confidence and burden: a CanCORS study . Cancer . 2017 ; 123 ( 22 ): 4481 – 4487 . doi: 10.1002/cncr.30875 28727147 PMC5673528

178. Ge L , Mordiffi SZ . Factors associated with higher caregiver burden among family caregivers of elderly cancer patients: a systematic review . Cancer Nurs . 2017 ; 40 ( 6 ): 471 – 478 . doi: 10.1097/NCC.0000000000000445 29045247

179. Thana K , Lehto R , Sikorskii A , Wyatt G . Informal caregiver burden for solid tumour cancer patients: a review and future directions . Psychol Health . 2021 ; 36 ( 12 ): 1514 – 1535 . doi: 10.1080/08870446.2020.1867136 33393827 PMC8254816

180. Zarit S , Todd P , Zarit J . Subjective burdens of husbands and wives as caregivers: a longitudinal study :. Alzheimer Dis Assoc Disord . 1987 ; 1 ( 2 ): 109 – 110 . doi: 10.1097/00002093-198701020-00026

181. Jayani R , Hurria A . Caregivers of older adults with cancer . Semin Oncol Nurs . 2012 ; 28 ( 4 ): 221 – 225 . doi: 10.1016/j.soncn.2012.09.004 23107179 PMC4096853

182. Kehoe LA , Xu H , Duberstein P , Quality of life of caregivers of older patients with advanced cancer . J Am Geriatr Soc . 2019 ; 67 ( 5 ): 969 – 977 . doi: 10.1111/jgs.15862 30924548 PMC7818364

183. Kadambi SG , Stupia L , Wang L , Feasibility of the geriatric assessment in older caregivers of older adults with cancer to guide supportive care . JCO Oncol Pract . 2023 ; 19 ( 11 suppl ): 224 – 224 . doi: 10.1200/OP.2023.19.11_suppl.224

184. Navaie‐Waliser M , Feldman PH , Gould DA , Levine C , Kuerbis AN , Donelan K . When the caregiver needs care: the plight of vulnerable caregivers . Am J Public Health . 2002 ; 92 ( 3 ): 409 – 413 . doi: 10.2105/AJPH.92.3.409 11867321 PMC1447090

185. Schulz R , Beach SR . Caregiving as a risk factor for mortality: the Caregiver Health Effects study . JAMA . 1999 ; 282 ( 23 ): 2215 . doi: 10.1001/jama.282.23.2215 10605972

186. Beesley VL , Price MA , Webb PM . Loss of lifestyle: health behaviour and weight changes after becoming a caregiver of a family member diagnosed with ovarian cancer . Support Care Cancer . 2011 ; 19 ( 12 ): 1949 – 1956 . doi: 10.1007/s00520-010-1035-2 21125296

187. National Alliance for Caregiving . Evercare® Study of Caregivers in Decline: A Close‐up Look at the Health Risks of Caring for a Loved One . Evercare ; 2006 .

188. Kuzuya M , Enoki H , Hasegawa J , Impact of caregiver burden on adverse health outcomes in community‐dwelling dependent older care recipients . Am J Geriatr Psychiatry . 2011 ; 19 ( 4 ): 382 – 391 . doi: 10.1097/JGP.0b013e3181e9b98d 20808120

189. Tsai CF , Lee YT , Lee WJ , Hwang JP , Wang SJ , Fuh JL . Depression of family caregivers is associated with disagreements on life‐sustaining preferences for treating patients with dementia . PLoS One . 2015 ; 10 ( 7 ): e0133711 . doi: 10.1371/journal.pone.0133711 PMC4521939 26230958

190. Epstein‐Lubow G , Gaudiano BA , Hinckley M , Salloway S , Miller IW . Evidence for the validity of the American Medical Association’s caregiver self‐assessment questionnaire as a screening measure for depression . J Am Geriatr Soc . 2010 ; 58 ( 2 ): 387 – 388 . doi: 10.1111/j.1532-5415.2009.02701.x 20370867

191. Thornton M , Travis SS . Analysis of the reliability of the modified caregiver strain index . J Gerontol B Psychol Sci Soc Sci . 2003 ; 58 ( 2 ): S127 – S132 . doi: 10.1093/geronb/58.2.S127 12646602

192. Shaffer KM , Benvengo S , Zalket AK , Feasibility and acceptability of distress screening for family caregivers at a cancer surgery center . Oncol Nurs Forum . 2019 ; 46 ( 2 ): 159 – 169 . doi: 10.1188/19.ONF.159-169 30767970 PMC6461406

193. Ugalde A , Gaskin CJ , Rankin NM , A systematic review of cancer caregiver interventions: appraising the potential for implementation of evidence into practice . Psychooncology . 2019 ; 28 ( 4 ): 687 – 701 . doi: 10.1002/pon.5018 30716183 PMC6594143

194. Chow R , Mathews JJ , Cheng EY , Interventions to improve outcomes for caregivers of patients with advanced cancer: a meta‐analysis . J Natl Cancer Inst . 2023 ; 115 ( 8 ): 896 – 908 . doi: 10.1093/jnci/djad075 37279594 PMC10407714

195. Northouse LL , Katapodi MC , Song L , Zhang L , Mood DW . Interventions with family caregivers of cancer patients: meta‐analysis of randomized trials . CA Cancer J Clin . 2010 ; 60 ( 5 ): 317 – 339 . doi: 10.3322/caac.20081 20709946 PMC2946584

196. Thomas TH , Campbell GB , Lee YJ , Priorities to improve cancer caregiving: report of a caregiver stakeholder workshop . Support Care Cancer . 2021 ; 29 ( 5 ): 2423 – 2434 . doi: 10.1007/s00520-020-05760-y 32918611 PMC7952464

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты