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      Premature Physiologic Aging as a Paradigm for Understanding Increased Risk of Adverse Health Across the Lifespan of Survivors of Childhood Cancer

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          Abstract

          The improvement in survival of childhood cancer observed across the past 50 years has resulted in a growing acknowledgment that simply extending the lifespan of survivors is not enough. It is incumbent on both the cancer research and the clinical care communities to also improve the health span of survivors. It is well established that aging adult survivors of childhood cancer are at increased risk of chronic health conditions, relative to the general population. However, as the first generation of survivors age into their 50s and 60s, it has become increasingly evident that this population is also at risk of early onset of physiologic aging. Geriatric measures have uncovered evidence of reduced strength and speed and increased fatigue, all components of frailty, among survivors with a median age of 33 years, which is similar to adults older than 65 years of age in the general population. Furthermore, frailty in survivors independently increased the risk of morbidity and mortality. Although there has been a paucity of research investigating the underlying biologic mechanisms for advanced physiologic age in survivors, results from geriatric populations suggest five biologically plausible mechanisms that may be potentiated by exposure to cancer therapies: increased cellular senescence, reduced telomere length, epigenetic modifications, somatic mutations, and mitochondrial DNA infidelity. There is now a critical need for research to elucidate the biologic mechanisms of premature aging in survivors of childhood cancer. This research could pave the way for new frontiers in the prevention of these life-changing outcomes.

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          Author and article information

          Journal
          J Clin Oncol
          J. Clin. Oncol
          jco
          jco
          JCO
          Journal of Clinical Oncology
          American Society of Clinical Oncology
          0732-183X
          1527-7755
          20 July 2018
          6 June 2018
          6 June 2018
          : 36
          : 21
          : 2206-2215
          Affiliations
          [1]Kirsten K. Ness, Zhaoming Wang, Mondira Kundu, Kelly McCastlain, Xiujie Li-Harms, Jinghui Zhang, and Gregory T. Armstrong, St. Jude Children’s Research Hospital, Memphis, TN; James L. Kirkland and Tamar Tchkonia, Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN; Maria Monica Gramatges, Texas Children’s Cancer and Hematology Centers at Baylor College of Medicine, Houston, TX; and Saskia Martine Francesca Pluijm, Princess Maxima Center for Pediatric Oncology, Utrecht, the Netherlands.
          Author notes
          Corresponding author: Kirsten K. Ness, MA, MPH, PhD, Mail Stop 735, St. Jude Children’s Research Hospital, 262 Danny Thomas Pl, Memphis, TN 38105; e-mail: kiri.ness@ 123456stjude.org .
          Article
          PMC6553838 PMC6553838 6553838 767467
          10.1200/JCO.2017.76.7467
          6553838
          29874132
          24acc23a-c832-4d76-9235-9b33aca09b40
          © 2018 by American Society of Clinical Oncology
          History
          Page count
          Figures: 5, Tables: 1, Equations: 0, References: 163, Pages: 12
          Categories
          PEDI24, Long Term Survival & Late Effects
          SPECIAL SERIES
          REVIEW ARTICLES
          Pediatric Oncology
          Custom metadata
          v1

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