Inverse birth cohort effects in ovarian cancer: Increasing risk in BRCA1/2 mutation carriers and decreasing risk in the general populationVos, J. R., Mourits, M. J., Teixeira, N., Jansen, L., Oosterwijk, J. C. & de Bock, G. H., Feb-2016, In : Gynecologic Oncology. 140, 2, p. 289-294 6 p.
Research output: Contribution to journal › Article › Academic › peer-review
Objective. BRCA1/2 carriers are at increased risk of ovarian cancer, and some reports suggest an increasing risk in more recent birth cohorts. In contrast, decreasing incidences have been observed in the general population. The aim was to assess the birth cohort effect on ovarian cancer risk in BRCA1/2 carriers relative to their background general population.
Methods. Data on ovarian cancer incidence was collected for a cohort of 1050 BRCA1/2 mutation carriers ascertained by our regional clinic and retrieved from the general Dutch population cancer registry. Birth cohorts were categorized as pre-1935, 1935-1953, post-1953. Birth cohort effects on the ovarian cancer risk were estimated using hazard ratios (HRs) in BRCA1/2 carriers and Poisson rate ratios in the general population. Standardized incidence ratios (SIRs) were calculated to compare populations. HRs were adjusted for mutation position and family history.
Results. Compared to the pre-1935 cohort, BRCA1 carriers in the 1935-1953 and post-1953 cohorts had an increased ovarian cancer risk of HRadjusted 1.54 (95% CI 1.11-2.14) and 2.40 (95% C11.56-3.69), respectively. BRC42 carriers in the 1935-1953 cohort had an HRadiusted of 3.01 (95% CI 1.47-6.13). The SIRs for the 1935-1953 and post-1953 cohorts were 1.7 and 2.7, respectively, for the BRCA1 carriers and 1.6 times and 2.4 times, respectively, for BRCA2 carriers.
Conclusions. Mutation carriers, particularly BRCA1 carriers, born in the most recent cohorts, have the highest additional ovarian cancer risk as compared to the general population. (C) 2015 Elsevier Inc. All rights reserved.
|Number of pages||6|
|Publication status||Published - Feb-2016|
- Ovarian cancer, BRCA1 gene, BRCA2 gene, Risk assessment, Birth cohort, BREAST-CANCER, COLLABORATIVE REANALYSIS, SALPINGO-OOPHORECTOMY, PHYSICAL-ACTIVITY, FAMILY-HISTORY, WOMEN, PENETRANCE, SERIES, PROPORTION, NUTRITION