Cancer Incidence in First- and Second-Degree Relatives of BRCA1 and BRCA2 Mutation Carriers. (15th June 2016)
- Record Type:
- Journal Article
- Title:
- Cancer Incidence in First- and Second-Degree Relatives of BRCA1 and BRCA2 Mutation Carriers. (15th June 2016)
- Main Title:
- Cancer Incidence in First- and Second-Degree Relatives of BRCA1 and BRCA2 Mutation Carriers
- Authors:
- Streff, Haley
Profato, Jessica
Ye, Yuanqing
Nebgen, Denise
Peterson, Susan K.
Singletary, Claire
Arun, Banu K.
Litton, Jennifer K. - Abstract:
- Abstract : Background: Mutations in the BRCA1 and BRCA2 genes are associated with increased risk of breast, ovarian, and several other cancers. The purpose of the present study was to evaluate the incidence of cancer in first- and second-degree relatives of BRCA mutation carriers compared with the general population. Materials and Methods: A total of 1, 086 pedigrees of BRCA mutation carriers was obtained from a prospectively maintained, internal review board-approved study of persons referred for clinical genetic counseling at the University of Texas MD Anderson Cancer Center. We identified 9, 032 first- and second-degree relatives from 784 pedigrees that had demonstrated a clear indication of parental origin of mutation. Standardized incidence ratios (SIRs) were used to compare the observed incidence of 20 primary cancer sites to the expected incidence of each cancer based on the calculated risk estimates according to each subject's age, sex, and ethnicity. Results: BRCA1 families had increased SIRs for breast and ovarian cancer ( p < .001) and decreased SIRs for kidney, lung, prostate, and thyroid cancer and non-Hodgkin's lymphoma ( p < .001). BRCA2 families had increased SIRs for breast, ovarian, and pancreatic cancer ( p < .001) and decreased SIRs for kidney, lung, thyroid, and uterine cancer and non-Hodgkin's lymphoma ( p < .0025). Analysis of only first-degree relatives ( n = 4, 099) identified no decreased SIRs and agreed with the increased SIRs observed in theAbstract : Background: Mutations in the BRCA1 and BRCA2 genes are associated with increased risk of breast, ovarian, and several other cancers. The purpose of the present study was to evaluate the incidence of cancer in first- and second-degree relatives of BRCA mutation carriers compared with the general population. Materials and Methods: A total of 1, 086 pedigrees of BRCA mutation carriers was obtained from a prospectively maintained, internal review board-approved study of persons referred for clinical genetic counseling at the University of Texas MD Anderson Cancer Center. We identified 9, 032 first- and second-degree relatives from 784 pedigrees that had demonstrated a clear indication of parental origin of mutation. Standardized incidence ratios (SIRs) were used to compare the observed incidence of 20 primary cancer sites to the expected incidence of each cancer based on the calculated risk estimates according to each subject's age, sex, and ethnicity. Results: BRCA1 families had increased SIRs for breast and ovarian cancer ( p < .001) and decreased SIRs for kidney, lung, prostate, and thyroid cancer and non-Hodgkin's lymphoma ( p < .001). BRCA2 families had increased SIRs for breast, ovarian, and pancreatic cancer ( p < .001) and decreased SIRs for kidney, lung, thyroid, and uterine cancer and non-Hodgkin's lymphoma ( p < .0025). Analysis of only first-degree relatives ( n = 4, 099) identified no decreased SIRs and agreed with the increased SIRs observed in the overall study population. Conclusion: We have confirmed previous reports of an association between breast, ovarian, and pancreatic cancers with BRCA mutations. Additional research to quantify the relative risks of these cancers for BRCA mutation carriers can help tailor recommendations for risk reduction and enhance genetic counseling. Abstract : Previous reports of an association between breast, ovarian, and pancreatic cancers with BRCA mutations have been confirmed. Additional research to quantify the relative risks of these cancers for BRCA mutation carriers can help tailor recommendations for risk reduction and enhance genetic counseling. … (more)
- Is Part Of:
- Oncologist. Volume 21:Number 7(2016)
- Journal:
- Oncologist
- Issue:
- Volume 21:Number 7(2016)
- Issue Display:
- Volume 21, Issue 7 (2016)
- Year:
- 2016
- Volume:
- 21
- Issue:
- 7
- Issue Sort Value:
- 2016-0021-0007-0000
- Page Start:
- 869
- Page End:
- 874
- Publication Date:
- 2016-06-15
- Subjects:
- BRCA -- Genetic counseling -- Familial cancers -- Breast cancer -- Ovarian cancer -- Pancreatic cancer
Oncology -- Periodicals
Tumors -- Periodicals
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Oncology
Tumors
Neoplasms
Electronic journals
Periodicals
Periodicals
616.994 - Journal URLs:
- https://academic.oup.com/oncolo ↗
https://theoncologist.onlinelibrary.wiley.com/journal/1549490x ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1634/theoncologist.2015-0354 ↗
- Languages:
- English
- ISSNs:
- 1083-7159
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6256.890000
British Library DSC - BLDSS-3PM
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- 20726.xml