Ontology highlight
ABSTRACT: Purpose
There are deficient data on prevalence of germline mutations in breast cancer susceptibility genes 1 and 2 (BRCA1/BRCA2) in Indian patients with ovarian cancer who are not selected by clinical features.Methods
This prospective, cross-sectional, noninterventional study in nine Indian centers included patients with newly diagnosed or relapsed epithelial ovarian, primary peritoneal, or fallopian tube cancer. The primary objective was to assess the prevalence of BRCA1/BRCA2 mutations, and the secondary objective was to correlate BRCA1/BRCA2 status with clinicopathologic characteristics. Mutation testing was performed by a standard next-generation sequencing assay.Results
Between March 2018 and December 2018, 239 patients
SUBMITTER: Gupta S
PROVIDER: S-EPMC8457852 | biostudies-literature | 2021 Jun
REPOSITORIES: biostudies-literature