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BRCA1/2 mutation carriers vs the general breast cancer population (N = 799,986): 21-gene assay-based molecular characterization.

Authors :
Yerushalmi R
Pomerantz A
Lewin R
Paluch-Shimon S
Soussan-Gutman L
Baehner FL
Voet H
Bareket-Samish A
Kedar I
Goldberg Y
Peretz-Yablonski T
Kadouri L
Source :
Breast cancer research and treatment [Breast Cancer Res Treat] 2024 Jul; Vol. 206 (1), pp. 67-76. Date of Electronic Publication: 2024 Apr 03.
Publication Year :
2024

Abstract

Purpose: We compared 21-gene recurrence score (RS) distribution and expression of the single-gene/gene groups within this assay between BC patients with pathogenic variants (PV) in BRCA1/2 vs the general 21-gene-tested BC population.<br />Methods: This retrospective study included consecutive 21-gene-tested female ER + HER2-negative BC patients with germline PVs in BRCA1/2. RS/gene expression data were compared to a previously described commercial use database (CDB, N = 799,986). Chi-square and 1-sample t test were used to compare RS distribution and single-gene/gene group scores between the study group and the CDB.<br />Results: Study group patients (N = 81) were younger and their RS results were higher compared to the CDB (age: median [IQR], 56 [47-61.5] vs 60 [51-67] years; p < 0.001; proportion of patients with RS ≥ 26: 49.4% vs 16.4%, p < 0.001). Expression of 12/16 cancer genes in the assay and the ER, proliferation, and invasion gene group scores differed significantly between the study group and the CDB, all in a direction contributing to higher RS. The differences between the study group and the CDB were mostly retained, upon stratifying the patients by menopausal status.<br />Conclusion: BC patients with PVs in BRCA1/2 have higher RS results that stem from distinct gene expression profiles in the majority of genes in the 21-gene assay.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1573-7217
Volume :
206
Issue :
1
Database :
MEDLINE
Journal :
Breast cancer research and treatment
Publication Type :
Academic Journal
Accession number :
38568368
Full Text :
https://doi.org/10.1007/s10549-024-07271-4