Candido-dos-Reis Francisco J, Song Honglin, Goode Ellen L, Cunningham Julie M, Fridley Brooke L, Larson Melissa C, Alsop Kathryn, Dicks Ed, Harrington Patricia, Ramus Susan J, de Fazio Anna, Mitchell Gillian, Fereday Sian, Bolton Kelly L, Gourley Charlie, Michie Caroline, Karlan Beth, Lester Jenny, Walsh Christine, Cass Ilana, Olsson Håkan, Gore Martin, Benitez Javier J, Garcia Maria J, Andrulis Irene, Mulligan Anna Marie, Glendon Gord, Blanco Ignacio, Lazaro Conxi, Whittemore Alice S, McGuire Valerie, Sieh Weiva, Montagna Marco, Alducci Elisa, Sadetzki Siegal, Chetrit Angela, Kwong Ava, Kjaer Susanne K, Jensen Allan, Høgdall Estrid, Neuhausen Susan, Nussbaum Robert, Daly Mary, Greene Mark H, Mai Phuong L, Loud Jennifer T, Moysich Kirsten, Toland Amanda E, Lambrechts Diether, Ellis Steve, Frost Debra, Brenton James D, Tischkowitz Marc, Easton Douglas F, Antoniou Antonis, Chenevix-Trench Georgia, Gayther Simon A, Bowtell David, Pharoah Paul D P
Department of Gynecology and Obstetrics, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo, Brazil.
Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, United Kingdom.
Clin Cancer Res. 2015 Feb 1;21(3):652-7. doi: 10.1158/1078-0432.CCR-14-2497. Epub 2014 Nov 14.
To analyze the effect of germline mutations in BRCA1 and BRCA2 on mortality in patients with ovarian cancer up to 10 years after diagnosis.
We used unpublished survival time data for 2,242 patients from two case-control studies and extended survival time data for 4,314 patients from previously reported studies. All participants had been screened for deleterious germline mutations in BRCA1 and BRCA2. Survival time was analyzed for the combined data using Cox proportional hazard models with BRCA1 and BRCA2 as time-varying covariates. Competing risks were analyzed using Fine and Gray model.
The combined 10-year overall survival rate was 30% [95% confidence interval (CI), 28%-31%] for non-carriers, 25% (95% CI, 22%-28%) for BRCA1 carriers, and 35% (95% CI, 30%-41%) for BRCA2 carriers. The HR for BRCA1 was 0.53 at time zero and increased over time becoming greater than one at 4.8 years. For BRCA2, the HR was 0.42 at time zero and increased over time (predicted to become greater than 1 at 10.5 years). The results were similar when restricted to 3,202 patients with high-grade serous tumors and to ovarian cancer-specific mortality.
BRCA1/2 mutations are associated with better short-term survival, but this advantage decreases over time and in BRCA1 carriers is eventually reversed. This may have important implications for therapy of both primary and relapsed disease and for analysis of long-term survival in clinical trials of new agents, particularly those that are effective in BRCA1/2 mutation carriers.
分析BRCA1和BRCA2种系突变对卵巢癌患者诊断后长达10年死亡率的影响。
我们使用了两项病例对照研究中2242例患者未发表的生存时间数据,以及先前报道研究中4314例患者的延长生存时间数据。所有参与者均接受了BRCA1和BRCA2有害种系突变的筛查。使用Cox比例风险模型,将BRCA1和BRCA2作为时变协变量,对合并数据的生存时间进行分析。使用Fine和Gray模型分析竞争风险。
非携带者的10年总生存率合并为30%[95%置信区间(CI),28%-31%],BRCA1携带者为25%(95%CI,22%-28%),BRCA2携带者为35%(95%CI,30%-41%)。BRCA1在时间为零时的风险比为0.53,并随时间增加,在4.8年时大于1。对于BRCA2,风险比在时间为零时为0.42,并随时间增加(预计在10.5年时大于1)。当仅限于3202例高级别浆液性肿瘤患者和卵巢癌特异性死亡率时,结果相似。
BRCA1/2突变与较好的短期生存相关,但这种优势会随着时间的推移而降低,在BRCA1携带者中最终会逆转。这可能对原发性和复发性疾病的治疗以及新药临床试验中的长期生存分析具有重要意义,特别是那些对BRCA1/2突变携带者有效的药物。