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21‐gene expression assay and clinical outcomes of premenopausal patients with hormone receptor‐positive breast cancer.

Authors :
Hyung, Jaewon
Lee, Sae Byul
Kim, Jisun
Kim, Hee Jeong
Ko, BeomSeok
Lee, Jong Won
Son, Byung‐Ho
Lee, Hee Jin
Gong, Gyungyub
Jeong, Hyehyun
Jeong, Jae Ho
Kim, Jeong Eun
Ahn, Jin‐Hee
Jung, Kyung Hae
Kim, Sung‐Bae
Source :
International Journal of Cancer; Feb2024, Vol. 154 Issue 4, p748-756, 9p
Publication Year :
2024

Abstract

The prognostic role of the recurrence score (RS) based on the 21‐gene expression assay in premenopausal women is not well delineated, and we investigated the association of outcomes and the RS in premenopausal patients who had 21‐gene expression assay at Asan Medical Center, Seoul, Korea, between June 2005 and July 2018. Invasive breast cancer‐free survival (IBCFS) by STEEP version 2.0 was compared according to the RS and clinical risk factors. A total of 554 patients were included in our study and 116 patients (20.9%) had age <40 years, 238 patients (43.0%) had luminal B subtype (Ki67 ≥ 20%), and 83 patients (15.0%) had RS >25. All patients received adjuvant tamoxifen ± chemotherapy. Overall, patients with RS >25 showed trend toward worse IBCFS from multivariable analysis (adjusted HR 1.89 [95% CI: 0.95‐3.73], P =.069). When comparing outcomes according to age and luminal subtypes, patients with luminal B subtype and age <40 years (n = 60) showed significantly worse outcomes compared to the others (luminal A or luminal B + age ≥40 years, n = 494; adjusted HR 2.95 [95% CI: 1.49‐5.82], log‐rank P <.001). Among patients with luminal B subtype and age <40 years, there was no significant association observed between IBCFS and the RS (log‐rank P =.51). In conclusion, while RS >25 showed association with poor outcomes in premenopausal women, it may have less prognostic significance among those with luminal B subtype and age <40 years. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00207136
Volume :
154
Issue :
4
Database :
Complementary Index
Journal :
International Journal of Cancer
Publication Type :
Academic Journal
Accession number :
174325538
Full Text :
https://doi.org/10.1002/ijc.34728