Improved survival in BRCA2 carriers with ovarian cancer

被引:55
作者
Pal, Tuya
Permuth-Wey, Jenny
Kapoor, Rachna
Cantor, Alan
Sutphen, Rebecca
机构
[1] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, MRC,CANCONT,Div Canc Prevent & Control, Tampa, FL 33612 USA
[2] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Biostat Core, Tampa, FL 33612 USA
[3] Univ S Florida, Coll Med, Dept Interdisciplinary Oncol, Tampa, FL USA
[4] Univ S Florida, All Childrens Hosp, Dept Pediat, St Petersburg, FL 33701 USA
关键词
hereditary ovarian cancer carcinoma; BRCA1; BRCA2; Survival;
D O I
10.1007/s10689-006-9112-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objectives The objective of this study was to investigate survival of ovarian cancer patients with BRCA1 and BRCA2 mutations compared to those without mutations in a population-based sample of incident epithelial ovarian cancer cases. Methods Follow-up for vital status was performed on a population-based sample of 232 women with incident epithelial ovarian cancer recruited between December 13, 2000 and September 30, 2003 in the Tampa Bay area. Survival analysis using Cox regression was performed on (1) all 232 cases and (2) the 209 invasive epithelial ovarian cancer cases. Results of the two analyses were similar, thus data involving the 209 invasive epithelial cancer cases are presented, as this was judged to be more clinically relevant. Results In the multivariate analysis, BRCA status and stage were statistically significant, and were adjusted for in the survival analysis model. The Kaplan-Meier method estimated expected survival at 4 years of 83% of BRCA2 carriers compared to 37% of BRCA1 carriers and 12% of non-carriers. There was a statistically significant difference between BRCA2 carriers and non-carriers (p = 0.013). No statistically significant survival differences were seen for BRCA1 carriers when compared with either BRCA2 carriers or non-carriers. Conclusion These data suggest that BRCA2 mutation carriers with ovarian cancer may have better survival than BRCA1 carriers and non-carriers. The etiology of this possible survival advantage is currently unknown. Larger studies are needed to confirm these results and to clarify their etiology and clinical significance.
引用
收藏
页码:113 / 119
页数:7
相关论文
共 50 条
[1]
Aida H, 1998, CLIN CANCER RES, V4, P235
[2]
*AM CANC SOC INC, 2005, CANC FACTS FIG 2005
[3]
Characteristics of BRCA1 mutations in a population-based case series of breast and ovarian cancer [J].
Anton-Culver, H ;
Cohen, PF ;
Gildea, ME ;
Ziogas, A .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (10) :1200-1208
[4]
Effect of BRCA mutations on the length of survival in epithelial ovarian tumors [J].
Ben David, Y ;
Chetrit, A ;
Hirsh-Yechezkel, G ;
Friedman, E ;
Beck, BD ;
Beller, U ;
Ben-Baruch, G ;
Fishman, A ;
Levavi, H ;
Lubin, F ;
Menczer, J ;
Piura, B ;
Struewing, JP ;
Modan, B .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (02) :463-466
[5]
Berchuck A, 1998, CLIN CANCER RES, V4, P2433
[6]
BRCA1 mutations in ovarian cancer and borderline tumours in Norway:: a nested case-control study [J].
Bjorge, T ;
Lie, AK ;
Hovig, E ;
Gislefoss, RE ;
Hansen, S ;
Jellum, E ;
Langseth, H ;
Nustad, K ;
Tropé, CG ;
Dorum, A .
BRITISH JOURNAL OF CANCER, 2004, 91 (10) :1829-1834
[7]
Clinicopathologic features of BRCA-linked and sporadic ovarian cancer [J].
Boyd, J ;
Sonoda, Y ;
Federici, MG ;
Bogomolniy, F ;
Rhei, E ;
Maresco, DL ;
Saigo, PE ;
Almadrones, LA ;
Barakat, RR ;
Brown, CL ;
Chi, DS ;
Curtin, JP ;
Poynor, EA ;
Hoskins, WJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (17) :2260-2265
[8]
FAMILIAL OVARIAN-CANCER [J].
BULLER, RE ;
ANDERSON, B ;
CONNOR, JP ;
ROBINSON, R .
GYNECOLOGIC ONCOLOGY, 1993, 51 (02) :160-166
[9]
Improved survival in women with BRCA-associated ovarian carcinoma [J].
Cass, I ;
Baldwin, RL ;
Varkey, T ;
Moslehi, R ;
Narod, SA ;
Karlan, BY .
CANCER, 2003, 97 (09) :2187-2195
[10]
Requirement of ATM-dependent phosphorylation of BRCA1 in the DNA damage response to double-strand breaks [J].
Cortez, D ;
Wang, Y ;
Qin, J ;
Elledge, SJ .
SCIENCE, 1999, 286 (5442) :1162-1166