Men with BRCA2 mutations have been found to be at increased risk of developing prostate cancer. There is a recent report that BRCA2 carriers with prostate cancer have poorer survival than noncarrier prostate cancer patients. In this study, we compared survival of men with a BRCA2 mutation and prostate cancer with that of men with a BRCA1 mutation and prostate cancer. We obtained the age at diagnosis, age at death or current age from 182 men with prostate cancer from families with a BRCA2 mutation and from 119 men with prostate cancer from families with a BRCA1 mutation. The median survival from diagnosis was 4.0 years for men with a BRCA2 mutation vs 8.0 years for men with a BRCA1 mutation, and the difference was highly significant (P<0.01). It may be important to develop targeted chemotherapies to treat prostate cancer in men with a BRCA2 mutation

Rapid progression of prostate cancer in men with a BRCA2 mutation

PASINI, Barbara;
2008-01-01

Abstract

Men with BRCA2 mutations have been found to be at increased risk of developing prostate cancer. There is a recent report that BRCA2 carriers with prostate cancer have poorer survival than noncarrier prostate cancer patients. In this study, we compared survival of men with a BRCA2 mutation and prostate cancer with that of men with a BRCA1 mutation and prostate cancer. We obtained the age at diagnosis, age at death or current age from 182 men with prostate cancer from families with a BRCA2 mutation and from 119 men with prostate cancer from families with a BRCA1 mutation. The median survival from diagnosis was 4.0 years for men with a BRCA2 mutation vs 8.0 years for men with a BRCA1 mutation, and the difference was highly significant (P<0.01). It may be important to develop targeted chemotherapies to treat prostate cancer in men with a BRCA2 mutation
2008
99(2)
2
371
374
http://www.nature.com/bjc/journal/v99/n2/pdf/6604453a.pdf
prostate cancer; BRCA1; BRCA2
Narod, Sa; Neuhausen, S; Vichodez, G; Armel, S; Lynch, Ht; Ghadirian, P; Cummings, S; Olopade, O; Stoppa-Lyonnet, D; Couch, F; Wagner, T; Warner, E; Foulkes, Wd; Saal, H; Weitzel, J; Tulman, A; Poll, A; Nam, R; Sun, P; Hereditary, Breast Cancer Study Group; Danquah, J; Domchek, S; Tung, N; Ainsworth, P; Horsman, D; Kim-Sing, C; Maugard, C; Eisen, A; Daly, M; Mckinnon, W; Wood, M; Isaacs, C; Gilchrist, D; Karlan, B; Nedelcu, R; Meschino, W; Garber, J; Pasini, B; Manoukian, S; Bellati, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/58117
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