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Risk factors for ovarian cancers with and without microsatellite instability.

Publication ,  Journal Article
Segev, Y; Pal, T; Rosen, B; McLaughlin, JR; Sellers, TA; Risch, HA; Zhang, S; Sun, P; Narod, SA; Schildkraut, J
Published in: Int J Gynecol Cancer
May 2014

OBJECTIVE: In a population-based sample of epithelial ovarian cancers, the objective of this study was to evaluate the association between microsatellite instability (MSI) status and the following factors: (1) ovarian cancer risk factors and (2) the distribution of the specific histologic subtypes. PATIENTS AND 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 the MSI status. Patients were divided into 3 groups (MSI-high, MSI-low, and MSI-stable) according to the 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 cases of cancer (13.8%) 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 significance differences among the groups. Among the 29 patients with BRCA1 mutations, 20.7% had MSI-high cancers compared with 5.9% among 17 patients with BRCA2 mutations. The proportions of different ovarian cancer histologies 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 histologies. 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.

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Published In

Int J Gynecol Cancer

DOI

EISSN

1525-1438

Publication Date

May 2014

Volume

24

Issue

4

Start / End Page

664 / 669

Location

England

Related Subject Headings

  • United States
  • Syndrome
  • Risk Factors
  • Prognosis
  • Ovarian Neoplasms
  • Oncology & Carcinogenesis
  • Neoplasm Staging
  • Mutation
  • Middle Aged
  • Microsatellite Repeats
 

Citation

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Chicago
ICMJE
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Segev, Y., Pal, T., Rosen, B., McLaughlin, J. R., Sellers, T. A., Risch, H. A., … Schildkraut, J. (2014). Risk factors for ovarian cancers with and without microsatellite instability. Int J Gynecol Cancer, 24(4), 664–669. https://doi.org/10.1097/IGC.0000000000000134
Segev, Yakir, Tuya Pal, Barry Rosen, John R. McLaughlin, Thomas A. Sellers, Harvey A. Risch, Shiyu Zhang, Ping Sun, Steven A. Narod, and Joellen Schildkraut. “Risk factors for ovarian cancers with and without microsatellite instability.Int J Gynecol Cancer 24, no. 4 (May 2014): 664–69. https://doi.org/10.1097/IGC.0000000000000134.
Segev Y, Pal T, Rosen B, McLaughlin JR, Sellers TA, Risch HA, et al. Risk factors for ovarian cancers with and without microsatellite instability. Int J Gynecol Cancer. 2014 May;24(4):664–9.
Segev, Yakir, et al. “Risk factors for ovarian cancers with and without microsatellite instability.Int J Gynecol Cancer, vol. 24, no. 4, May 2014, pp. 664–69. Pubmed, doi:10.1097/IGC.0000000000000134.
Segev Y, Pal T, Rosen B, McLaughlin JR, Sellers TA, Risch HA, Zhang S, Sun P, Narod SA, Schildkraut J. Risk factors for ovarian cancers with and without microsatellite instability. Int J Gynecol Cancer. 2014 May;24(4):664–669.
Journal cover image

Published In

Int J Gynecol Cancer

DOI

EISSN

1525-1438

Publication Date

May 2014

Volume

24

Issue

4

Start / End Page

664 / 669

Location

England

Related Subject Headings

  • United States
  • Syndrome
  • Risk Factors
  • Prognosis
  • Ovarian Neoplasms
  • Oncology & Carcinogenesis
  • Neoplasm Staging
  • Mutation
  • Middle Aged
  • Microsatellite Repeats