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Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026

Accelerated aging and risk of subsequent neoplasms in survivors of childhood cancer: a report from the Childhood Cancer Survivor Study.

СтатьяНазвание и аннотация: Перевод в очереди
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Berkman Amy M, Bhatia Shalini, Mirzaei Sedigheh, Li Kendrick, Im Cindy, Leisenring Wendy M, Williams AnnaLynn M, Esbenshade Adam J, Hayek Samah, Chow Eric J, Turcotte Lucie M, Neglia Joseph P, Arnold Michael A, Srivastava Deokumar, Nolan Vikki G, Ness Kirsten K, Hudson Melissa M, Armstrong Gregory T

Аннотация

BACKGROUND: Survivors of childhood cancer face elevated risks for treatment‑related late effects, including subsequent malignant neoplasms (SMNs). In the general population, accelerated aging is associated with increased malignancy risk, however this has not been evaluated in survivors.

METHODS: Survivors enrolled in the Childhood Cancer Survivor Study with measures of physiologic frailty, Cumulative Illness Burden for Geriatrics (CIRS-G), or Deficit Accumulation Index (DAI) data were included. Associations between these measures of accelerated aging with SMNs, benign meningiomas, and non-melanoma skin cancers (NMSC) were estimated with piecewise exponential models, adjusted for sociodemographic, treatment, and modifiable factors.

RESULTS: Physiologic frailty and CIRS‑G were not associated with risk of SMNs, meningiomas, or NMSCs. Higher DAI was only associated with increased risk of benign meningioma, but not SMNs or NMSCs.

CONCLUSIONS: Accelerated aging measures were not consistently associated with SMN risk in survivors of childhood cancer.

IMPACT: Our results confirm that established risk factors, especially treatment exposures, remain critical in the development of SMN in survivors, reinforcing the importance of risk‑adapted therapies and long‑term surveillance in survivorship care.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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