2022 Chinese expert consensus and guidelines on clinical management of toxicity in anti-CD19 chimeric antigen receptor T-cell therapy for B-cell non-Hodgkin lymphoma.

Introduction

CAR T-cell therapy is a novel treatment approach for hematological malignancies 1 – 3 . Multiple CD19-targeted CAR T-cell products have been approved for the treatment of relapsed and/or refractory (r/r) B-cell non-Hodgkin lymphoma (B-NHL), including large B-cell lymphoma, follicular lymphoma, and mantle cell lymphoma, in the United States and Europe 4 – 7 . In China, 2 CAR T-cell products, axicabtagene ciloleucel 8 and relmacabtagene autoleucel 9 , have been approved for use in adults with r/r large B-cell lymphoma. In addition, the number of registered clinical trials of CAR T cells in China has substantially increased in the past 5 years, and surpassed that in the United States. With the development of novel CAR T-cell products 10 – 12 and innovative approaches, such as dual-target CAR T cells 13 – 15 and sequential infusions of CAR T cells targeting different antigens 16 – 18 , CAR T-cell therapy is anticipated to be widely used to treat various tumors beyond B-NHL in the near future.

With increased understanding of CAR T-cell properties and experience in treating patients with CAR T cells, clinicians are becoming more concerned about potentially life-threatening CAR T-cell-associated toxicities 19 – 22 . CAR T cells show dynamic differences among hematological malignancies 23 – 26 , and CAR T-cell-associated toxicities in B-NHL have distinguishing features such as local cytokine-release syndrome (L-CRS) 27 . Nevertheless, previously published CRS grading and management guidelines have provided few specific recommendations for managing these toxicities 28 – 30 . This consensus aims to provide clinicians with a standardized guideline and recommendations for the diagnosis, prevention, and treatment of toxicities in patients with B-NHL treated with CAR T-cell therapy.

The contents of the consensus are divided into 7 sections: the first section includes a workup and risk assessment for CAR T-cell-associated toxicities at baseline, and the other 6 sections outline various toxicities, including CRS, CAR-T-cell-associated encephalopathy syndrome (CRES), hemophagocytic lymphohistiocytosis/macrophage activation syndrome (HLH/MAS), and other adverse events (AEs). Because CRS is the most commonly observed AE in CAR T-cell therapy, its clinical management is emphasized herein.

Workup and risk assessment for toxicities at baseline

Essential workup procedures before CAR T-cell therapy should include a complete medical history and physical examination, with attention paid to node-bearing areas, evaluation of performance status, documentation of lymphoma classification and staging at diagnosis, previous treatments, and evaluation of opportunistic infections, as appropriate. Laboratory evaluations include complete blood count (CBC), urinalysis, blood chemistry profile, comprehensive metabolic panel, serum ferritin and lactate dehydrogenase, disseminated intravascular coagulation panel (including D-dimer, fibrinogen, prothrombin time, and partial thromboplastin time measurements), serum cytokine profile [including measurements for serum interleukin (IL) 6, tumor necrosis factor-α (TNF-α)], and C-reactive protein. Other recommended tests include hepatitis B/C virus, human immunodeficiency virus, and treponemia pallidum antibody evaluations. Epstein–Barr virus, cytomegalovirus and human herpes virus testing may be useful under certain circumstances. Imaging and other studies include chest/abdomen/pelvic computed tomography (CT) with contrast and/or whole body positron emission tomography/CT, brain magnetic resonance imaging (MRI), electrocardiography, and echocardiography. If any extranodal involvement, particularly in the bone marrow (BM), gastrointestinal (GI) tract, pleura/peritoneum, and central nervous system (CNS), is suspected, relevant examinations, including BM biopsy with aspirate, endoscopic ultrasound, and serosal and lumbar puncture to analyze serosal effusion and cerebrospinal fluid (CSF), should be performed. Organ function tests are recommended for patients with vital organ involvement. Optional workup procedures include BM cytogenetics (karyotype analysis) and pulmonary function tests.

The above workup is also designed to identify populations at higher risk of developing severe toxicities. These high-risk factors include the following: (1) ECOG ≥ 3 31 ; (2) age ≥ 70 years; (3) high tumor burden, i.e., the sum of the product of the perpendicular diameters of multiple lesions (SPD) ≥ 100 cm 2 32 ; (4) a bulky mass with diameter ≥ 10 cm; (5) a mass located in the pharynx or around the trachea, with compression symptoms; (6) a mass near luminal organs (e.g., the GI tract or bile duct), which may induce organ dysfunction because of tumor compression and infiltration; (7) serosal involvement with massive serous effusion (pleural/abdominal effusion); (8) hepatitis B antigen seropositivity, hepatitis B virus (HBV) DNA copy number above the upper limit of normal value, or active HBV infection without antiviral treatment; (9) involvement of vital organs (e.g., lung, kidney, or bone marrow); and (10) tumor-associated fever.

CRS

CRS is defined as a supraphysiologic immune response after immunotherapy that leads to overactivation of endogenous or infused T cells and other immune effector cells 29 , 33 , 34 . The incidence rate of CRS among patients with B-NHL treated with CAR T cells is 23%–93%. Among these patients, 2%–22% experience severe CRS (sCRS, grade 3 or higher) 8 , 35 , 36 .

The mechanism of CRS remains elusive. Recent studies have indicated that activated monocytes/macrophages but not CAR T cells are major contributors to CRS 37 , 38 , and that endothelial activation and macrophage-released catecholamines may involve amplification of cytokine release and enhancement of inflammatory injury during CAR T-cell therapy 39 , 40 . Yuying Liu et al. 41 have suggested that damage-associated molecular patterns released by pyroptotic cells may be upstream triggers of macrophage/macrophage activation. Direct contact between CAR T cells and macrophages through CD40-40 L 42 , CD69 43 , lymphocyte activation gene-3 44 , and TNF-α 45 may also play important roles in this process.

Classification and grading of CRS

Owing to its physiological features, CRS in B-NHL exhibits unique features 27 , 46 . Therefore, the classification and grading of CRS in B-NHL must be refined to help clinicians identify and manage this AE effectively.

CRS can be classified as acute CRS (1–3 weeks after infusion), late CRS (3–6 weeks after infusion), and chronic CRS (≥ 6 weeks after infusion) according to the onset time. CRS can also be classified as L-CRS or systemic CRS (S-CRS) according to the location and site, involved 27 , 47 ( Figure 1 ). During early stages of CAR T-cell therapy, the infused CAR T cells accumulate in the tumor, expand locally, and release several cytokines that in turn trigger a local inflammatory response, which is defined as L-CRS. Subsequently, the locally expanded CAR T cells and cytokines “overflow” into the circulatory system, thereby promoting S-CRS ( Figure 2 ).

L-CRS is frequently observed in patients with a high tumor burden or bulky mass, and it manifests as redness/swelling/enlargement and exudation/effusion in or around the lesion, or even perforation or bleeding at the lesion site. Unlike those of L-CRS, the clinical manifestations of S-CRS are characterized by fever, hypotension, and hypoxia, with or without organ dysfunction 27 , 47 – 49 . Given that the previously published CRS grading systems are based only on the severity of S-CRS symptoms, which may not be fully applicable to B-NHL, we propose a new CRS grading system that incorporates the specific manifestations of L-CRS 29 . The grades are defined by the presence of fever (≥38 °C), the severity of hemodynamic compromise, the severity of hypoxia and the severity of local inflammatory manifestations of lesions surrounding tissues and organs ( Table 1 ).

Monitoring and management of acute CRS

The peak window of CRS risk is typically the first 3 weeks after CAR T-cell infusion, which is a critical period for CRS management 30 . Thus, clinicians must closely monitor patients to ensure early diagnosis and prompt intervention for CRS. The workup includes a complete physical examination, with special attention to vital signs and lesion sites, assessment of organ systems, and laboratory tests 19 , 50 . Electrocardiographic monitoring is recommended from the time of CAR T-cell infusion until acute CRS is relieved. For patients with high risk of sCRS, this monitoring should continue for at least 3 weeks or until the high-risk factors are resolved. Laboratory tests include CBC, complete metabolic panel, blood chemistry profile, coagulation profile, serum ferritin, lactate dehydrogenase, serum cytokine profile, and CAR transgene copies (or CAR T-cell percentage in peripheral blood mononuclear cells), which must be rechecked at least 3 times per week for 2 weeks postinfusion, once per week for the next 2 weeks, and every 3 months thereafter. For patients with high sCRS risk, the above tests should be performed more frequently or even daily. Imaging studies to assess the lesions and involved organs may be considered for select patients.

Management of CRS in B-NHL should be performed in line with the grade of this toxicity, as shown in Table 2 . If CRS symptoms persist or become aggravated for more than 24 h, a management strategy for a higher CRS grade should be initiated immediately. Patient transfer to the intensive care unit (ICU) is recommended when sCRS develops. In general, patients with CRS are administered a combination of tocilizumab and corticosteroids, in addition to supportive care. For prolonged S-CRS or substantial symptoms or comorbidities, treatment with tocilizumab at 4–8 mg/kg (not exceeding 800 mg) is advised, and administration can be repeated after 6 h, as needed. Furthermore, the use of anti-TNF-α agents can be considered if L-CRS is present or for persistent and refractory fever. For patients with grade 4 or persistent CRS despite anti-IL-6 and/or anti-TNF-α therapy, the use of corticosteroids may be considered. For patients with high risk of sCRS, β-receptor blockers should be administered from the day of CAR T-cell infusion 40 . Plasma exchange can be performed to treat emergent CRS. Additional supportive care includes antipyretic measures, intravenous fluid boluses, and/or vasopressors for patients with hypotension, and/or supplemental oxygen for those with hypoxia.

Severe CRS is typically associated with dysfunction in multiple vital organs, such as the heart, liver, and kidney, which can be fatal and should be thoroughly evaluated and properly managed. Of note, L-CRS may cause specific organ damage, depending on the location of the lesion 4 , 51 . When L-CRS occurs, patients with GI involvement or lesions around the GI tract may experience mucosal damage or even vascular rupture and bleeding at lesion sites 52 . Thus, tissue damage may provide more possibilities for the intestinal flora to promote S-CRS; consequently, gut purging and oral antibiotics to inhibit the intestinal flora before CAR T-cell therapy are recommended 53 . Prophylactic use of anti-TNF-α agents may also be considered when compression symptoms occur in patients with a mass around the trachea or serosal involvement, and anti-TNF-α therapy and local intervention, such as tracheotomy and drainage of serous effusion, should be performed. The heart is another organ requiring special attention 54 , 55 : cardiac function should be closely monitored when the tumor lesion is located around the heart 56 – 58 . Bridging therapy before CAR T-cell therapy is necessary for patients with this underlying risk. Detailed clinical management procedures for AEs in organs during L-CRS are shown in Table 3 .

Late CRS

Late CRS is generally considered delayed acute CRS, typically occurring within 3–6 weeks after CAR T-cell infusion 59 . Similarly to those of S-CRS, the clinical manifestations of late CRS are fever, cytopenia, elevated transaminase levels, coagulation disorders, increased CAR copy number, and residual tumors. Late CRS should be distinguished from lymphodepletion therapy-associated hematological toxicities, GI toxicities, and infections. The monitoring and management strategies for acute CRS are similar to those for late CRS.

Chronic CRS

Chronic CRS is defined as inflammation- or CAR T-cell-associated AEs that occur after 6 weeks of CAR T-cell infusion 29 , 60 , 61 . The clinical manifestations of chronic CRS include (1) intermittent low-grade fever (below 38 °C); (2) fatigue and anepithymia; (3) cytopenia, particularly thrombocytopenia; (4) CAR T-cell re-expansion in the peripheral blood; (5) residual tumors; and (6) interstitial pneumonitis or bronchiectasis-like manifestations in some patients. Chronic CRS should be distinguished from infections and hematological toxicity 59 , 62 . Management of chronic CRS includes anti-TNF-α agents for treatment of pulmonary symptoms and supportive care 63 . CBC should be monitored closely, and component blood transfusion can be performed for supportive care in select patients.

CAR T-cell-associated encephalopathy syndrome

CRES is another common AE that occurs with CAR T-cell therapy and is characterized by a pathological CNS process after therapy 29 , 64 , 65 . Although the pathophysiological mechanism of CRES remains unclear, its severity has been shown to be associated with high levels of serum cytokines, high tumor burden, disruption of the blood brain barrier, CAR structure, and brain mural cells expressing CD19 66 , 67 .

According to published data, the incidence of CRES is 20%–64%, and 5%–28% of cases in patients with B-NHL who receive CAR T-cell therapy are of grade 3 or higher 28 , 35 , 36 , 68 – 70 . CRES typically occurs within 8 weeks after CAR T-cell infusion, with a median duration of 4–6 days. Neurological symptoms of CRES include headache, agitation, cognitive dysfunction, tremors, ataxia, language disturbance, somnolence, papilloedema, and seizures 30 , 71 , 72 , and secondary cerebral edema is a leading cause of death 47 , 73 .

Distinguishing CRES from cerebrovascular events such as cerebral hemorrhage and infarction is crucial, because thrombocytopenia and coagulation disorders frequently occur after CAR T-cell therapy 74 . Medical history inquiry and brain MRI examination may be useful. Single epileptic seizures often occur in some patients after CAR T-cell therapy. Clinicians should be cautious when diagnosing CRES, particularly in patients with a history of cerebrovascular accidents and seizures in this context.

According to the CAR-T-cell-therapy-associated toxicity (CARTOX) CRES grading scale 30 , grade is defined by the CARTOX-10 score, elevated intracranial pressure, and seizures/motor weakness. Workup for grading CRES includes a thorough neurological evaluation through fundoscopic examination and electroencephalography (EEG), neuroimaging assessment through MRI or CT scans, and measurement of CSF pressure 30 . Similarly to CRS, CRES management should be based on the appropriate toxicity grade, as shown in Table 4 . In addition to supportive care, corticosteroids are the cornerstone of the management strategy for CRES. However, tocilizumab is not recommended for treating CRES unless CRS is concurrent. ICU monitoring is recommended for patients with grade 3 or 4 CRES. For patients with a history of seizures or a high risk of CRES, prophylactic use of levetiracetam can be implemented before CAR T-cell therapy 73 , 75 .

Hemophagocytic lymphohistiocytosis/macrophage activation syndrome

HLH/MAS are a group of severe immunological diseases characterized by excessive activation of T cells and macrophages, lymphohistiocytic tissue infiltration, and immune-mediated multiorgan dysfunction 76 – 78 . CAR T-cell-associated HLH/MAS usually occurs during the recovery phase of CRS or accompanies CRS 29 , 78 , 79 . Compared with S-CRS, HLH/MAS has characteristic clinical manifestations that include hepatosplenomegaly; hemophagocytes and hemophagocytosis in the bone marrow; cytopenia in at least 2 hematopoietic cell lineages; hypertriglyceridemia; and elevated serum levels of ferritin, cytokines, and soluble CD25 80 – 82 . HLH/MAS may result in prolonged leukopenia or neutropenia, thus increasing the risk of serious infection. The early phase of HLH/MAS is easily overlooked, because the features also frequently occur in CRS, infection, and bone marrow suppression after CAR T-cell therapy 29 , 30 . HLH/MAS should be suspected in the presence of the following conditions 78 , 80 – 84 : high levels of blood CAR T cells for more than 2 weeks and again after 2 weeks; recurrent fever with cytopenia or hepatosplenomegaly; and sustained increases in serum ferritin. To date, standard clinical management of HLH/MAS in patients treated with CAR T-cell therapy is not well established. According to cumulative experience from multiple domestic centers and consultation with experts with experience in treating this toxicity, we provide the following recommendations for clinical management of HLH/MAS 81 – 84 : (1) closely monitor vital signs and CBC in patients after CAR T-cell therapy; (2) closely monitor serum concentrations of ferritin and triglyceride; (3) HLH/MAS should be suspected if a patient has unexplained fever and cytopenia after CAR T-cell infusion; (4) if HLH/MAS is diagnosed, additional therapy with low-dose etoposide (50–100 mg/m 2 per week) is recommended; (5) JAK-2 inhibitors (ruxolitinib), CTLA-4 agonists (abatacept), and anti-CD52 antibodies (alemtuzumab) can be used for select patients; (6) plasma exchange may be considered in emergencies; and (7) use of novel agents, such as anti-interferon-γ antibody, may be considered under certain circumstances.

Bone marrow suppression

Cytopenia caused by bone marrow suppression is one of the most common AEs in patients after CAR T-cell therapy 70 , 85 – 87 ; the incidence of grade 3–4 neutropenia, anemia, and thrombocytopenia is 45%–69%, 30%–37%, and 15%–30%, respectively 9 , 35 , 88 . At least 15% of patients experience prolonged severe cytopenia beyond 3 months 85 , 86 .

Given that cytopenia increases risks of infection and relevant complications (e.g., cerebral hemorrhage), the following management measures should be performed according to its grade: (1) prophylaxis for bacterial and fungal infections until severe leukopenia or neutropenia resolves; (2) supplemental low-flow oxygen and packed red blood cell transfusion for patients with severe anemia; (3) prophylactic use of hemostatic agents and platelet transfusion for patients with severe thrombocytopenia; and (4) additional preventive measures (e.g., room disinfection by ultraviolet light or use of a soft toothbrush) for patients with any grade of leukopenia or thrombocytopenia.

Infection

Infections after CAR T-cell therapy are common and are reported in as many as 70% of patients 9 , 36 , 59 , 89 ; as many as 40% of these infections occur within the first month 79 . The most common infections are bacterial (16%–30%), and these usually occur within the first 2 weeks. Factors that may contribute to infection include lymphodepletion or prior chemotherapy, CAR T-cell-mediated B-cell aplasia/hypogammaglobulinemia, and prolonged cytopenia.

In such cases, the manifestations of infections can mimic CRS in terms of fever, hypotension, and hypoxia, thus posing a major diagnostic dilemma 29 , 30 , 90 , 91 . Nonetheless, no biomarkers are available to differentiate the 2 disorders. Moreover, because infections usually occur in the context of CRS and may exacerbate CRS, early identification and timely intervention are crucial. One previous study has indicated that the distinct signature for severe infections includes a double peak of serum IL-6 levels, and high serum levels of IL-8 and IL-1β, which may aid in differential diagnosis between severe infection and CRS 51 , 79 . If CRS and infection are not distinguishable, we recommend that the combination of CRS treatment and antimicrobial prophylaxis be considered.

During CAR T-cell therapy, concurrent infections may complicate CAR T-cell-associated toxicities, including CRS and neurotoxicity. Moreover, approximately 10% of severe or life-threatening infections may occur during and after the lymphodepletion period. For patients with active or uncontrolled infection at baseline, CAR T-cell therapy cannot be initiated until the infection is resolved 21 , 70 . Prophylaxis against Pneumocystis jirovecii pneumonia and zoster reactivation is generally applied before lymphodepletion therapy and for 3 months thereafter 51 , 92 – 94 . Of note, CAR-T therapy may pose a risk of HBV reactivation in carriers. For HBV carriers, prophylactic use of entecavir should be initiated before lymphodepletion therapy and continue for at least 6 months. Monthly follow-up to monitor HBV DNA levels is also necessary for early detection of HBV reactivation 95 , 96 . The decision to provide prophylaxis against bacterial or fungal infections should be risk-adjusted on the basis of patient characteristics, such as prior hematopoietic stem cell transplantation and infection history. After lymphodepletion chemotherapy, the use of granulocyte colony-stimulating factor 97 can be considered when neutrophil counts decrease to < 0.5 × 10 9 /L. If infection is suspected, empiric broad-spectrum antibacterial therapy should be initiated immediately 98 . Empiric antifungal therapy is usually added after 4–7 days in patients expected to have persistent neutropenia.

Infections that occur at specific sites (skin and soft tissue, urinary system, and catheter-associated infections) are more common with CAR T-cell-mediated systemic immunosuppression, in contrast to other antitumor therapies. Of note, infections of the skin and soft tissue or serosal involvement by tumors may be severe and aggravated by concurrent L-CRS. The management principles for special-site infections are provided in Table 5 .

Other toxicities

B-cell aplasia/hypogammaglobulinemia

Prolonged B-cell aplasia/hypogammaglobulinemia, an anticipated on-target, off-tumor toxicity, is a characteristic adverse effect after CAR T-cell therapy 51 , 99 that can be diagnosed according to absolute B-cell counts < 61 cells/μL and serum immunoglobulin G (IgG) ≤ 400 mg/dL 100 . Almost all patients who receive CAR T-cell therapy experience varying degrees of B-cell deficiency 36 , 70 , thus increasing the risk of humoral immunity dysfunction-associated infections. Prophylactic intravenous injection of human immunoglobulin (IVIG) is a routine adjuvant treatment for patients who receive CAR T-cell therapy. The practical algorithm for management of hypogammaglobulinemia is as follows 93 :

Replacement with monthly IVIG until recovery of B cells to the normal range or 6 months after CAR T-cell infusion.

For patients with serum IgG ≤ 400 mg/dL and serious or recurrent infection, monthly IVIG replacement should continue until risk factors are eliminated.

Regular monitoring of serum levels of IgG, IgM and IgA and blood CD19+ or CD20+ B-cell counts is recommended for patients at high risk of infection.

Tumor lysis syndromes

Tumor lysis syndromes (TLS) are a group of disorders caused by rapid release of large amounts of intracellular contents and metabolites into the systemic circulation 101 , 102 . Clinical manifestations of TLS include hyperuricemia, hyperphosphatemia, hypocalcemia, hyperkalemia, and acute renal insufficiency. Diagnostic criteria for TLS include (1) a 25% increase in the levels of serum potassium; (2) a 25% decrease in calcium levels; (3) serum creatinine > 221 μmol/L; (4) 25% increase in the levels of serum uric acid or urea nitrogen; and (5) cardiac arrhythmia and renal failure in some patients 103 , 104 .

TLS prophylaxis should be considered for patients with high tumor burden (SPD ≥ 100 cm 2 or bulky mass with diameter ≥ 10 cm) or high tumor proliferation activity (Ki67 ≥ 85%) 101 , 102 . We recommend that hydration and alkalization be initiated 24 h before lymphodepletion therapy, and if necessary, diuretics be used to ensure a urine volume > 3,000 mL/day. Sodium bicarbonate may be administered to maintain urine pH in 7.0–7.5.

The foundation of TLS treatment includes (1) frequent monitoring of electrocardiography, blood pressure, and oxygen saturation; (2) adequate intravenous hydration (≥3,000 mL/day) to maintain urine volume (≥3,000 mL/day), with diuretics used if necessary; (3) sodium bicarbonate administered to ensure urine pH between 7.0 and 7.5; (4) correction of fluid and electrolyte disturbances; (5) allopurinol or febuxostat for treatment of hyperuricemia; and (6) hemodialysis for patients who develop renal failure with uncorrected electrolyte disorder 101 , 102 , 104 , 105 .

Hypersensitivity reactions

The incidence of infusion-associated allergic reactions is relatively low (up to 3%), and allergic shock rarely occurs. In general, allergic reactions can be easily mistaken for a secondary symptom of other AEs. For example, skin rash usually occurs within the first 2 weeks after CAR T-cell infusion and resolves spontaneously within 3–5 days. In addition to allergies, skin rash may be attributable to CRS-induced increased fragility of the capillary endothelium. The population at high risk of developing allergic reactions includes those who may be hypersensitive to (1) in vitro culture reagents during CAR T production, (2) viral vector impurity, and (3) T-cell activation resulting from a pre-CAR T unresolved inflammatory background.

Management principles include the following: (1) exclusion of patients with hypersensitivity at enrollment; (2) strict control of the procedure and reagents during CAR T-cell manufacturing; (3) antimicrobial therapy before infusion to eliminate an in vivo inflammatory background; and (4) prophylactic use of anti-allergic agents (e.g., diphenhydramine or promethazine) 106 .

Excessive CAR T-cell proliferation

CAR T-cell levels should be monitored within the first month after CAR T-cell infusion. Blood samples should be collected once every 2–3 days within the first 2 weeks and once per week thereafter. Excessive CAR T-cell proliferation should be highly suspected under the following conditions 107 : (1) white blood cell counts in peripheral blood ≥ 10 × 10 9 /L; (2) lymphocyte percentage in white blood cells ≥ 70%; and (3) absolute CAR+ T-cell counts > 600 cells/μL. Indications that should be considered for identifying this condition include the following:

Is the expansion of CAR T cells consistent with the changes in tumor size?

Do CAR T cells localize to or expand at other sites in additional to the peripheral blood?

Is the uncontrolled proliferation of activated T cells caused by viral infection?

Management practices to control excessive CAR T-cell proliferation include glucocorticoids and other immunosuppressive agents (e.g., anti-thymocyte globulin or anti-CD52 antibodies). A combination of 2 or more immunosuppressive agents may be used in severe cases.

Secondary malignancies

On the basis of previous studies, the incidence of secondary malignancies after CAR T-cell therapy is approximately 15% 59 , 108 , a percentage similar to that of patients receiving other antitumor therapies 109 – 113 . Acute myeloid leukemia and myelodysplastic syndromes are the most commonly observed secondary hematologic malignancies 28 , 59 , 108 . Secondary malignancies usually develop after the first year of CAR T-cell therapy 114 , 115 , and regular follow-up is important for early recognition of these disorders after CAR T-cell therapy. Some studies have suggested that combination therapy with epigenetic drugs, such as decitabine, may improve patient prognosis.

Conclusions

CAR T-cell therapy is a potentially curative treatment for patients with r/r B-NHL. However, CAR T-cell-associated toxicities may decrease the survival benefit from CAR T-cell therapy. To date, a thorough recommendation for management of CAR T-associated toxicities in B-NHL is lacking. In response to this need, we compiled this consensus on the basis of our current understanding and clinical experience from multiple domestic institutions. The consensus refines the CRS grading system and classification and provides comprehensive and detailed practice recommendations for grading, monitoring, and managing toxicities observed in CAR T-cell therapy for B-NHL. We hope that the consensus will be useful for CAR T-cell therapy for B-NHL by helping clinicians effectively manage CAR T-cell-associated toxicities.

The consensus has several limitations. First, most of the evidence provided was derived from clinical studies on CAR T cells, mostly targeting CD19, yet toxicity profiles and features can vary across CAR T-cell products and individuals. Second, some exploratory recommendations proposed herein are based on case/case series reports or clinical experience, without sufficient evidence. Future multicenter prospective clinical trials and real-world studies are needed to develop more appropriate toxicity mitigation and optimization strategies.

Grant support

This work was supported by funds from the National Natural Science Foundation of China (Grant Nos. 81830002, 81830004, 82070168, and 32070951), the Translational Research grant of NCRCH (Grant No. 2020ZKZC04), and National Key R&D Program of China (Grant No. 2021YFA1100800).

Conflict of interest statement

No potential conflicts of interest are disclosed.

Author contributions

Conceived and designed the analysis: Aibin Liang, Weidong Han, Wenbin Qian.

Collected the data: Ping Li, Yang Liu, Yajing Zhang, Fengxia Shi, Yun Liang.

Contributed data or analysis tools: Aibin Liang, Weidong Han, Wenbin Qian, Ping Li, Yang Liu, Yun Liang, Jian Bo, Sujun Gao, Yongxian Hu, Yu Hu, He Huang, Xiaojun Huang, Hongmei Jing, Xiaoyan Ke, Jianyong Li, Yuhua Li, Qifa Liu, Peihua Lu, Heng Mei, Ting Niu, Yongping Song, Yuqin Song, Liping Su, Sanfang Tu, Jianxiang Wang, Depei Wu, Zhao Wang, Kailin Xu, Zhitao Ying, Qingming Yang, Yajing Zhang, Fengxia Shi, Bin Zhang, Huilai Zhang, Xi Zhang, Mingfeng Zhao, Weili Zhao, Xiangyu Zhao, Liang Huang, Jun Zhu.

Performed the analysis: Ping Li, Yang Liu, Yajing Zhang, Fengxia Shi, Yun Liang.

Wrote the paper: Ping Li, Yang Liu, Yajing Zhang, Fengxia Shi, Yun Liang.

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