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Mini Oral session: Breast cancer

4MO - Prognostic implication of 21-gene expression assay in luminal B type hormone receptor-positive breast cancer patients younger than 40 years

Date

03 Dec 2022

Session

Mini Oral session: Breast cancer

Topics

Tumour Site

Breast Cancer

Presenters

Jaewon Hyung

Citation

Annals of Oncology (2022) 33 (suppl_9): S1431-S1435. 10.1016/annonc/annonc1118

Authors

J. Hyung1, S. Lee2, J. Kim2, H.J. Kim2, B. Ko2, B. Son2, J. Lee2, H.J. Lee3, G. Gong3, H. Lee1, H. Jeong1, J. Jeong1, J.E. Kim1, J. Ahn1, K.H. Jung1, S. Kim1

Author affiliations

  • 1 Oncology, Asan Medical Center, 138-931 - Seoul/KR
  • 2 Surgery, Asan Medical Center, 138-736 - Seoul/KR
  • 3 Pathology, Asan Medical Center, 138-931 - Seoul/KR

Resources

This content is available to ESMO members and event participants.

Abstract 4MO

Background

Recurrence score (RS) based on 21-gene expression assay is widely used to evaluate prognosis and potential benefits of adjuvant chemotherapy (AC) for hormone-receptor positive (HR+) breast cancer (BC) patients (pts). In this study, we investigated clinical significance of RS in premenopausal HR+ BC pts.

Methods

HR+ BC pts with age < 50 years at diagnosis who had at least 3 years of follow-up duration from surgery and had 21-gene expression assay in Asan Medical Center, Seoul, Korea, between June 2005 to July 2018 were included. Recurrence-free survival (RFS) by STEEP version 2.0 was compared according to the RS and other clinicopathologic variables.

Results

Among total 567 pts included in this analysis, 117 pts (20.6%) had age < 40 years and 238 pts (42.0%) had luminal B type BC (LB) by 4-IHC, 85 pts (15.0%) had RS > 25, 301 pts (53.8%) had high clinical risk BC as defined by tumor size, lymph node and histologic grade and 92 pts (16.2%) had AC. On univariate analysis, pts with RS > 25 showed poor RFS (log-rank, p = 0.007). Also, pts with age < 40 years (log-rank, p = 0.008), high clinical risk (log-rank, p = 0.030) and LB (log-rank, p = 0.002) had poor RFS. On multivariate analysis, age < 40 years and LB were associated with significantly poor RFS with HR of 2.49 (95% CI 1.16-5.36, p = 0.020) and 2.59 (95% CI 1.11-6.04, p = 0.028), respectively while RS > 25 was not associated with RFS. When compared according to age group (< 40 years vs. 40 years) and luminal types (luminal A (LA) vs. LB), pts with age < 40 years and LB showed significantly poor RFS (HR 4.52, [95% CI 2.08-9.84], p < 0.001) compared to pts with age 40 years or LA. Pts with < 40 years with LB had higher proportion of pts who received AC (35.0% vs. 14.0%, p < 0.001) compared to pts with age 40 years or LA. While RS > 25 was associated with poor RFS among pts with age 40 years or LA (HR 3.20, [95% CI 1.20-8.53], p = 0.020), RS > 25 was not associated with RFS in pts with age < 40 years and LB (HR 1.31, [95% CI 0.34-5.10], p = 0.699).

Conclusions

The RS alone was not prognostic among premenopausal HR+ BC pts especially with age < 40 years and LB, which showed significantly poor RFS compared to pts with age 40 years or LA despite of higher proportion of pts who received AC.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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