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  • Risks of first and subseque...
    Mai, Phuong L.; Best, Ana F.; Peters, June A.; DeCastro, Rosamma M.; Khincha, Payal P.; Loud, Jennifer T.; Bremer, Renée C.; Rosenberg, Philip S.; Savage, Sharon A.

    Cancer, December 1, 2016, Letnik: 122, Številka: 23
    Journal Article

    BACKGROUND Li‐Fraumeni syndrome (LFS) is an autosomal dominant cancer predisposition syndrome characterized by a very high lifetime cancer risk and an early age at diagnosis of a wide cancer spectrum. Precise estimates for the risk of first and subsequent cancers are lacking. METHODS The National Cancer Institute's Li‐Fraumeni Syndrome Study includes families meeting the diagnostic criteria for LFS or Li‐Fraumeni‐like syndrome, and individuals with a germline TP53 mutation, choroid plexus carcinoma, adrenocortical carcinoma, or ≥3 cancers. Herein, we estimated the cumulative risk and annual hazards for first and second cancers among TP53 mutation carriers (TP53 positive TP53+) using MATLAB statistical software. RESULTS This study evaluated 286 TP53+ individuals from 107 families. The cumulative cancer incidence was 50% by age 31 years among TP53+ females and 46 years among males, and nearly 100% by age 70 years for both sexes. Cancer risk was highest after age 20 years for females, mostly due to breast cancer, whereas among males the risk was higher in childhood and later adulthood. Among females, the cumulative incidence rates by age 70 years for breast cancer, soft tissue sarcoma, brain cancer, and osteosarcoma were 54%, 15%, 6%, and 5%, respectively. Among males, the incidence rates were 22%, 19%, and 11%, respectively, for soft tissue sarcoma, brain cancer, and osteosarcoma. Approximately 49% of those with 1 cancer developed at least another cancer after a median of 10 years. The average age‐specific risk of developing a second cancer was comparable to that of developing a first cancer. CONCLUSIONS The cumulative cancer risk in TP53 + individuals was very high and varied by sex, age, and cancer type. Additional work, including prospective risk estimates, is needed to better inform personalized risk management. Cancer 2016;122:3673‐81. © 2016 American Cancer Society. In this study, the cumulative cancer risk among individuals with a germline TP53‐positive mutation appears to be high and varies by sex, age, and cancer type. Approximately 50% of those with one cancer developed at least one other cancer, at an average age‐specific risk comparable to that of the first cancer.