# Survival outcomes in trial defined high-risk hormone receptor-positive/human epidermal growth factor receptor II-negative early breast cancer: impact of adjuvant chemotherapy

**Authors:** Ta-Chung Chao, Deanna Gracia, Chan-Heng Ho, Hao-Yang Chen, Chi-Cheng Huang, Ling-Ming Tseng

PMC · DOI: 10.1007/s12672-025-02601-4 · Discover Oncology · 2025-05-16

## TL;DR

This study examines survival outcomes in high-risk hormone receptor-positive breast cancer patients and the impact of adjuvant chemotherapy.

## Contribution

The study identifies distinct high-risk subgroups and evaluates chemotherapy's effectiveness in these subgroups.

## Key findings

- Adjuvant chemotherapy reduced recurrence risk in M-high patients (HR: 0.24).
- Chemotherapy showed no benefit for N-high patients except stage III cases (HR: 0.2).
- M-low/N-high patients had better survival outcomes (96.8% OS) compared to M-high/N-high (94.8% OS).

## Abstract

Clinical trials have shown the efficacy of adding CDK4/6 inhibitors to standard endocrine therapy in hormone receptor (HR)-positive, human epidermal growth factor receptor II (HER2)-negative high-risk early breast cancer.

HR+ /HER2− early breast cancers were retrieved from cancer registry. The primary endpoints were overall survival (OS) and recurrence-free survival (RFS) among trial-defined high-risk patients, as well as the impact of adjuvant chemotherapy.

Among 2758 registered cases, 511 and 1207 patients met MonarchE (M) and NATALEE (N) high-risk criteria, respectively. OS was 94.8% for M-high/N-high, 96.8% for M-low/N-high, 90.7% for M-high/N-low, and 98.9% for M-low/N-low patients, with a hazard ratio (HR) of 2.3 and 2.8 for M-high and N-high, respectively. For RFS, chemotherapy reduced recurrence risk in M-high patients (HR: 0.24) but showed no benefit for N-high patients overall, except for stage III N-high cases (HR: 0.2).

Adjuvant chemotherapy significantly reduced recurrence risk in M-high patients with early breast cancer. Further stratification of M-low/N-high patients is needed to guide tailored chemotherapy approaches alongside CDK4/6 inhibition.

The online version contains supplementary material available at 10.1007/s12672-025-02601-4.

## Linked entities

- **Proteins:** Cdk4 (Cyclin-dependent kinase 4)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}
- **Diseases:** cancer (MESH:D009369), breast cancer (MESH:D001943), III N (MESH:C536631)
- **Chemicals:** CDK4/6 inhibitors (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12084447