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PMID: 22274685 已发表 · ppublish 英语

Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer.

JAMA ·第 307 卷 ·第 4 期 ·2012-01-26

Bolton Kelly L, Chenevix-Trench Georgia, Goh Cindy, Sadetzki Siegal, Ramus Susan J, Karlan Beth Y, Lambrechts Diether, Despierre Evelyn, Barrowdale Daniel, McGuffog Lesley, Healey Sue, Easton Douglas F, Sinilnikova Olga, Benítez Javier, García María J, Neuhausen Susan, Gail Mitchell H, Hartge Patricia, Peock Susan, Frost Debra, Evans D Gareth, Eeles Rosalind, Godwin Andrew K, Daly Mary B, Kwong Ava, Ma Edmond S K, Lázaro Conxi, Blanco Ignacio, Montagna Marco, D'Andrea Emma, Nicoletto Maria Ornella, Johnatty Sharon E, Kjær Susanne Krüger, Jensen Allan, Høgdall Estrid, Goode Ellen L, Fridley Brooke L, Loud Jennifer T, Greene Mark H, Mai Phuong L, Chetrit Angela, Lubin Flora, Hirsh-Yechezkel Galit, Glendon Gord, Andrulis Irene L, Toland Amanda E, Senter Leigha, Gore Martin E, Gourley Charlie, Michie Caroline O, Song Honglin, Tyrer Jonathan, Whittemore Alice S, McGuire Valerie, Sieh Weiva, Kristoffersson Ulf, Olsson Håkan, Borg Åke, Levine Douglas A, Steele Linda, Beattie Mary S, Chan Salina, Nussbaum Robert L, Moysich Kirsten B, Gross Jenny, Cass Ilana, Walsh Christine, Li Andrew J, Leuchter Ronald, Gordon Ora, Garcia-Closas Montserrat, Gayther Simon A, Chanock Stephen J, Antoniou Antonis C, Pharoah Paul D P, , ,

摘要

Approximately 10% of women with invasive epithelial ovarian cancer (EOC) carry deleterious germline mutations in BRCA1 or BRCA2. A recent article suggested that BRCA2-related EOC was associated with an improved prognosis, but the effect of BRCA1 remains unclear.,To characterize the survival of BRCA carriers with EOC compared with noncarriers and to determine whether BRCA1 and BRCA2 carriers show similar survival patterns.,A pooled analysis of 26 observational studies on the survival of women with ovarian cancer, which included data from 1213 EOC cases with pathogenic germline mutations in BRCA1 (n = 909) or BRCA2 (n = 304) and from 2666 noncarriers recruited and followed up at variable times between 1987 and 2010 (the median year of diagnosis was 1998).,Five-year overall mortality.,The 5-year overall survival was 36% (95% CI, 34%-38%) for noncarriers, 44% (95% CI, 40%-48%) for BRCA1 carriers, and 52% (95% CI, 46%-58%) for BRCA2 carriers. After adjusting for study and year of diagnosis, BRCA1 and BRCA2 mutation carriers showed a more favorable survival than noncarriers (for BRCA1: hazard ratio [HR], 0.78; 95% CI, 0.68-0.89; P < .001; and for BRCA2: HR, 0.61; 95% CI, 0.50-0.76; P < .001). These survival differences remained after additional adjustment for stage, grade, histology, and age at diagnosis (for BRCA1: HR, 0.73; 95% CI, 0.64-0.84; P < .001; and for BRCA2: HR, 0.49; 95% CI, 0.39-0.61; P < .001). The BRCA1 HR estimate was significantly different from the HR estimated in the adjusted model (P for heterogeneity = .003).,Among patients with invasive EOC, having a germline mutation in BRCA1 or BRCA2 was associated with improved 5-year overall survival. BRCA2 carriers had the best prognosis.

文献信息
期刊
JAMA
期刊简称
JAMA
发表日期
2012-01-26
收录日期
2012-01-25
更新日期
2016-12-03
语言
英语
国家/地区
United States
NLM ID
7501160
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