RETRACTED: Risk Factors for Ovarian Cancers With and Without Microsatellite Instability (Retracted Article)

被引:5
作者
Segev, Yakir [1 ,2 ,3 ]
Pal, Tuya [1 ]
Rosen, Barry [2 ,3 ]
McLaughlin, John R. [4 ]
Sellers, Thomas A. [5 ]
Risch, Harvey A. [6 ]
Zhang, Shiyu [1 ]
Ping, Sun [1 ]
Narod, Steven A. [1 ]
Schildkraut, Joellen [7 ]
机构
[1] Womens Coll Res Inst, Familial Breast Canc Res, Toronto, ON M5G 1N8, Canada
[2] Univ Toronto, Canada Dept Obstet & Gynecol, Toronto, ON, Canada
[3] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[4] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[5] Univ S Florida, H Lee Moffitt Canc Ctr, Dept Canc Epidemiol, Tampa, FL 33682 USA
[6] Yale Univ, Sch Publ Hlth, Dept Chron Dis Epidemiol, New Haven, CT USA
[7] Duke Univ, Duke Sch Med, Durham, NC USA
关键词
Ovarian cancer; Microsatellite instability; Risk factors; MISMATCH REPAIR; BRCA2; MUTATIONS; TUBAL-LIGATION; CARRIERS; METAANALYSIS; WOMEN; CARCINOMAS; FREQUENCY; OBESITY; COHORT;
D O I
10.1097/IGC.0b013e31829a5527
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The objective of this study was to evaluate the association between microsatellite instability (MSI) status and (1) ovarian cancer risk factors and (2) the distribution of the specific histologic subtypes in a population-based sample of epithelial ovarian cancers. Methods: Participants were drawn from 3 population-based studies of primary epithelial ovarian cancer. Tumor DNA was analyzed using 5 standardized microsatellite markers to assess MSI status. Patients were divided into 3 groups (MSI-high, MSI-low, and MSI-stable) according to National Cancer Institute criteria. We compared the prevalence of specific known risk and protective factors among the 3 subgroups, including body mass index, smoking history, parity, BRCA1 and BRCA2 mutation status, past oral contraceptive use, and tubal ligation. Similarly, we compared the distribution of the histologic subtypes among the 3 subgroups. Results: A total of 917 ovarian cancer patients were included. One hundred twenty-seven (13.8%) cancers were MSI-high. Subgroup analyses according to smoking, body mass index, parity, past oral contraceptive use, and past tubal ligation did not reveal any statistically significant differences among the groups. Among the 29 patients with BRCA1 mutations, 20.7% had MSI-high cancers compared with 5.9% among 17 BRCA2-mutation patients. The proportions of different ovarian cancer histologic findings among the various MSI subgroups were similar. Conclusions: The prevalence of risk and protective factors among ovarian cancer patients is similar for cancers with and without MSI. The distributions of MSI do not differ significantly among ovarian cancers with different histologic findings. Ovarian cancer patients with BRCA1 mutations had a 21% rate of MSI-high tumors, compared with 6% among patients with BRCA2 mutations, but this difference was not statistically significant.
引用
收藏
页码:1010 / 1015
页数:6
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