TY - JOUR
T1 - Germline Mutations in 12 Genes and Risk of Ovarian Cancer in Three Population-Based Cohorts
AU - Kotsopoulos, Joanne
AU - Hathaway, Cassandra A.
AU - Narod, Steven A.
AU - Teras, Lauren R.
AU - Patel, Alpa V.
AU - Hu, Chunling
AU - Yadav, Siddhartha
AU - Couch, Fergus J.
AU - Tworoger, Shelley S.
N1 - Publisher Copyright:
©2023 American Association for Cancer Research.
PY - 2023/10/1
Y1 - 2023/10/1
N2 - Background: With the widespread use of multigene panel genetic testing, population-based studies are necessary to accurately assess penetrance in unselected individuals. We evaluated the prevalence of germline pathogenic or likely pathogenic variants (mutations) in 12 cancer-predisposition genes and associations with ovarian cancer risk in three population-based prospective studies [Nurses’ Health Study (NHS), NHSII, Cancer Prevention Study II]. Methods: We included women with epithelial ovarian or peritoneal cancer (n ¼ 776) and controls who were alive and had at least one intact ovary at the time of the matched case diagnosis (n ¼ 1,509). Germline DNA was sequenced for mutations in 12 genes. Conditional logistic regression was used to estimate odds ratios (OR) and 95% confidence intervals (CI) for ovarian cancer risk by mutation status. Results: The mutation frequency across all 12 genes was 11.2% in cases and 3.3% in controls (P < 0.0001). BRCA1 and BRCA2 were the most frequently mutated (3.5% and 3.8% of cases and 0.3% and 0.5% of controls, respectively) and were associated with increased ovarian cancer risk [OR, BRCA1 ¼ 12.38; 95% confidence interval (CI) ¼ 4.72–32.45; OR, BRCA2 ¼ 9.18; 95% CI ¼ 3.98–21.15]. Mutation frequencies for the other genes were ≤1.0% and only PALB2 was significantly associated with risk (OR ¼ 5.79; 95% CI ¼ 1.09–30.83). There was no difference in survival for women with a BRCA germline mutation versus no mutation. Conclusions: Further research is needed to better understand the role of other mutations in ovarian cancer among unselected populations. Impact: Our data support guidelines for germline genetic testing for BRCA1 and BRCA2 among women diagnosed with epithelial ovarian cancer; testing for PALB2 may be warranted.
AB - Background: With the widespread use of multigene panel genetic testing, population-based studies are necessary to accurately assess penetrance in unselected individuals. We evaluated the prevalence of germline pathogenic or likely pathogenic variants (mutations) in 12 cancer-predisposition genes and associations with ovarian cancer risk in three population-based prospective studies [Nurses’ Health Study (NHS), NHSII, Cancer Prevention Study II]. Methods: We included women with epithelial ovarian or peritoneal cancer (n ¼ 776) and controls who were alive and had at least one intact ovary at the time of the matched case diagnosis (n ¼ 1,509). Germline DNA was sequenced for mutations in 12 genes. Conditional logistic regression was used to estimate odds ratios (OR) and 95% confidence intervals (CI) for ovarian cancer risk by mutation status. Results: The mutation frequency across all 12 genes was 11.2% in cases and 3.3% in controls (P < 0.0001). BRCA1 and BRCA2 were the most frequently mutated (3.5% and 3.8% of cases and 0.3% and 0.5% of controls, respectively) and were associated with increased ovarian cancer risk [OR, BRCA1 ¼ 12.38; 95% confidence interval (CI) ¼ 4.72–32.45; OR, BRCA2 ¼ 9.18; 95% CI ¼ 3.98–21.15]. Mutation frequencies for the other genes were ≤1.0% and only PALB2 was significantly associated with risk (OR ¼ 5.79; 95% CI ¼ 1.09–30.83). There was no difference in survival for women with a BRCA germline mutation versus no mutation. Conclusions: Further research is needed to better understand the role of other mutations in ovarian cancer among unselected populations. Impact: Our data support guidelines for germline genetic testing for BRCA1 and BRCA2 among women diagnosed with epithelial ovarian cancer; testing for PALB2 may be warranted.
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U2 - 10.1158/1055-9965.EPI-23-0041
DO - 10.1158/1055-9965.EPI-23-0041
M3 - Article
C2 - 37493628
AN - SCOPUS:85173563205
SN - 1055-9965
VL - 32
SP - 1402
EP - 1410
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 10
ER -