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Review Series Open Access Address correspondence to: Shahrukh K. Phone: Find articles by Shafqat, S. Find articles by Arana Chicas, E. Find articles by Shafqat, A. Find articles by Hashmi, S. Published July 1, - More info. Recent improvements in cancer treatment have increased the lifespan of pediatric and adult cancer survivors.
However, cancer treatments accelerate aging in survivors, which manifests clinically as the premature onset of chronic diseases, such as endocrinopathies, osteoporosis, cardiac dysfunction, subsequent cancers, and geriatric syndromes of frailty, among others. Therefore, cancer treatment—induced early aging accounts for significant morbidity, mortality, and health expenditures among cancer survivors.
One major mechanism driving this accelerated aging is cellular senescence; cancer treatments induce cellular senescence in tumor cells and in normal, nontumor tissue, thereby helping mediate the onset of several chronic diseases.
Studies on clinical monitoring and therapeutic targeting of cellular senescence have made considerable progress in recent years. Large-scale clinical trials are currently evaluating senotherapeutic drugs, which inhibit or eliminate senescent cells to ameliorate cancer treatment—related aging.