Impact of germline BRCA1 mutations and overexpression of p53 on prognosis and response to treatment following breast carcinoma -: 10-year follow-up data

被引:86
作者
Goffin, JR
Chappuis, PO
Bégin, LR
Wong, N
Brunet, JS
Hamel, N
Paradis, AJ
Boyd, J
Foulkes, WD
机构
[1] McGill Univ, Ctr Hlth, Div Med Genet, Dept Med, Montreal, PQ, Canada
[2] McGill Univ, Dept Pathol & Surg, Montreal, PQ, Canada
[3] McGill Univ, Canc Prevent Ctr, Sir MB Davis Jewish Gen Hosp, Montreal, PQ, Canada
[4] Algorithme Pharma, Montreal, PQ, Canada
[5] McGill Univ, Program Canc Genet, Dept Oncol, Montreal, PQ, Canada
[6] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[7] McGill Univ, Inst Res, Ctr Hlth, Montreal, PQ, Canada
[8] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10021 USA
[9] McGill Univ, Dept Oncol, Montreal, PQ, Canada
关键词
breast neoplasms; BRCA1; protein p53; adjuvant chemotherapy; tamoxifen; prognosis; neoplastic syndromes; hereditary;
D O I
10.1002/cncr.11080
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Overexpression of p53 has been associated with poor survival following breast carcinoma. BRCAI interacts biochemically with p53 and may also contribute to poor outcome when constitutionally mutated. The joint effect of both abnormalities has not been studied. The primary objective of this study was to assess the impact of germline BRCA1 mutations and p53 overexpression on survival after 10 years of follow-up. METHODS. A historical cohort of Ashkenazi Jewish women 65 years or younger with invasive breast carcinoma was tested for BRCA1 founder mutations. p53 overexpression was assessed by immunohistochemistry. Clinicopathologic information was obtained by chart review. RESULTS. in total, 278 women were analyzed. On univariate analysis, p53 overexpression (n = 63) was prognostic for worse overall survival (relative risk [RR] 2.6, P = 0.001) whereas BRCA1 germline mutations (n = 30) were of borderline significance (RR 1.9, P = 0.052). In the lymph node-negative subpopulation, BRCAI mutation status conferred a higher mortality on univariate (RR 5.6, P < 0.001) and multivariate (RR 3.5, P = 0.03) analyses. There was a trend in favor of a worse prognosis for women who carried a germline BRCA1 mutation and whose tumor overexpressed p53. When compared with noncarriers, BRCAI mutation carriers had a worse overall survival if they did not receive adjuvant chemotherapy (RR 3.3, P= 0.01) or adjuvant hormonal therapy (RR 2.3, P = 0.02). CONCLUSIONS. Germline BRCA1 mutations and p53 overexpresion carry a negative prognosis that is not additive to known prognostic factors. Given the experimental sensitivity of BRCA1-mutated cells to chemotherapy, the worse survival among BRCA1 mutation-carrying lymph node-negative breast carcinoma patients may be partly explained by the significantly lower proportion of lymph node-negative patients who received adjuvant chemotherapy (P < 0.001). Cancer 2003;97: 527-36. (C) 2003 American Cancer Society.
引用
收藏
页码:527 / 536
页数:10
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