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May 29, 2026Journal of Clinical Oncology0 citations

Real-world evaluation of germline pathogenic variants (PVs) in cancer-predisposition genes among unselected South Asian women with breast or ovarian cancer.

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SYSiddhartha YadavRPRaja PramanikRSRamila Shilpakar

Key Points

  • To validate the frequency of germline pathogenic variants in cancer-predisposition genes among unselected South Asian women with breast or ovarian cancer.
  • Pooled data from two prospective cohorts: SARAH Consortium and NuGenA.
  • Analyzed 1,711 women with histologically confirmed breast or ovarian cancer, collecting personal and family history questionnaires and blood samples for genetic testing.
  • Identified pathogenic variants in multiple cancer predisposition genes using a multigene panel.
  • Germline pathogenic variants found in 17.7% of breast and 35.9% of ovarian cancer cases.
  • BRCA1/2 pathogenic variants accounted for 13.6% of breast and 28.3% of ovarian cancer cases.
  • Among BRCA1/2 carriers, 74.2% did not report a family history of cancer.

Abstract

10513 Background: Prior reports of high frequency of BRCA1 and BRCA2 ( BRCA1/2 ) PVs among South Asian women from Bangladesh, India, Nepal, and Pakistan with breast or ovarian cancer require validation in large prospective unselected cohorts. Methods: Individual-level anonymized patient data from two prospective cohorts were pooled to evaluate the prevalence of germline PVs among South Asian women: the South Asian Regional Alliance for Hereditary Cancers (SARAH Consortium) in Bangladesh, Nepal, and Pakistan, and the previously reported Nurse-led Genetic Counseling and Awareness (NuGenA) expansion cohort in India. Both studies enrolled consecutive cases of histologically confirmed newly diagnosed breast or epithelial ovarian cancer irrespective of age at diagnosis or family history. In both studies, participants completed questionnaires on personal and family history (first-, second- or third-degree) and provided blood for germline genetic testing after written consent. PVs in cancer predisposition genes including ATM, BARD1, BRCA1, BRCA2, BRIP1, CHEK2, MLH1, MSH2, MSH6, PALB2, RAD51C, RAD51D, and TP53 were identified as part of the studies utilizing a multigene panel and the results were returned to ordering clinicians. The data cutoff date for this analysis was November 30, 2025. Results: The analysis included 1,711 South Asian women with breast (n=1,210) or ovarian (n=501) cancer. A family history of breast or ovarian cancer was noted in 177 (10.3%). Among breast cancers, 94% were invasive, 84% were ductal, 35% were triple-negative and over two-thirds presented with nodal involvement. Germline PVs across 13 predisposition genes were observed in 17.7% of breast and 35.9% of ovarian cancers. Notably, BRCA1/2 PVs accounted for most of these PV (13.6% of breast and 28.3% of ovarian cancer cases) with PVs in all genes except BRCA1/2 under 1%. The frequency of BRCA1/2 PVs was 24.4% in triple-negative breast cancer and 8.0% in ER+/HER2-. BRCA1/2 PV carriers were diagnosed with breast cancer at a younger age than non-carriers (Median age: 42 vs 46 years, P<0.001), with no age difference observed in ovarian cancer (50 vs. 51 years, P=0.79). Notably, among the 306 BRCA1/2 PV carriers identified, 229 (74.2%) did not report a family history of breast or ovarian cancer. Conclusions: We confirm a high prevalence of BRCA1/2 PVs among unselected South Asian women with either breast or ovarian cancer. The observations of younger age at cancer diagnosis, and low rates of family history support the need for population-specific germline genetic testing and risk management strategies in South Asia.

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Cite This Study

Yadav et al. (2026) studied this question.

synapsesocial.com/papers/6a192d7efab5b468c4416545https://doi.org/10.1200/jco.2026.44.16_suppl.10513
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Spectrum of germline pathogenic and novel BRCA1 and BRCA2 gene mutations in a cohort of 1780 breast and ovarian carcinoma patients from east India.2026
  2. 2Prevalence of germline cancer predisposition pathogenic variants in cancer cohorts.2026
  3. 3PREVALENCE OF BRCA1 AND BRCA2 MUTATIONS IN WOMEN WITH EARLY-ONSET BREAST CANCER2025
  4. 4Abstract PS10-02: Association between Germline Mutation Status and Overall Survival among Women with Breast Cancer in Population-based Studies in the United States2024
  5. 5Abstract PO3-09-04: Identification of germline pathogenic variants to guide systemic therapy: Prevalence and spectrum of PVs among Mexican patients with metastatic breast cancer2024