# Impact of HER2-Low Expression on Clinical Outcomes in Metastatic Breast Cancer Treated with CDK4/6 Inhibitors

**Authors:** Şahin Bedir, Tanju Kapagan, Burçin Çakan Demirel, Merve Tokocin, Çiğdem Yıldırım, Semra Taş, Yakup Bozkaya, Abdilkerim Oyman, Nilufer Bulut, Gökmen Umut Erdem

PMC · DOI: 10.3390/jcm15051898 · 2026-03-02

## TL;DR

This study found that low HER2 expression in breast cancer patients treated with CDK4/6 inhibitors does not affect treatment response or survival.

## Contribution

The study clarifies that HER2-low status has no prognostic or predictive value in HR+/HER2− metastatic breast cancer treated with CDK4/6 inhibitors.

## Key findings

- HER2-low and HER2-zero patients had similar overall response rates to CDK4/6 inhibitors.
- There was no significant difference in progression-free survival between HER2-low and HER2-zero patients.
- HER2 status did not independently predict overall survival in multivariable analyses.

## Abstract

Background: The prognostic significance of low-level human epidermal growth factor receptor 2 (HER2) expression in hormone receptor-positive/HER2-negative (HR+/HER2−) metastatic breast cancer remains unclear, particularly in patients treated with cyclin-dependent kinase 4/6 inhibitors (CDK4/6i). This study aimed to evaluate the impact of HER2-low status on treatment response and survival outcomes in this setting. Methods: This multicenter retrospective cohort study included patients with HR+/HER2− metastatic breast cancer who received first-line endocrine therapy combined with palbociclib or ribociclib between January 2018 and May 2025. HER2-low tumors were defined as immunohistochemistry (IHC) 1+ or 2+ with negative in situ hybridization, while HER2-zero tumors were classified as IHC 0. Treatment response, progression-free survival (PFS), and overall survival (OS) were compared between groups using Kaplan–Meier analysis and Cox regression models. Results: A total of 309 patients were analyzed, including 122 (39.5%) with HER2-low disease and 187 (60.5%) with HER2-zero disease. Baseline clinicopathological characteristics were well balanced between groups. The overall response rate was 75.4% in the HER2-low group and 72.7% in the HER2-zero group (p > 0.05). Median PFS was 23.9 months for HER2-low patients and 25.2 months for HER2-zero patients (log-rank p = 0.785). Median OS was 49.5 and 53.1 months, respectively, with no statistically significant difference (log-rank p = 0.649). HER2 status was not an independent predictor of PFS or OS in multivariable analyses. Conclusions: In patients with HR+/HER2− metastatic breast cancer treated with first-line endocrine therapy plus CDK4/6 inhibitors, HER2-low expression was not associated with differences in treatment response or survival outcomes. These findings suggest that HER2-low status does not have prognostic or predictive relevance in this endocrine-sensitive population.

## Linked entities

- **Proteins:** ERBB2 (erb-b2 receptor tyrosine kinase 2)
- **Chemicals:** palbociclib (PubChem CID 5330286), ribociclib (PubChem CID 44631912)
- **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:** Breast Cancer (MESH:D001943), tumors (MESH:D009369)
- **Chemicals:** CDK4/6 Inhibitors (-), ribociclib (MESH:C000589651), palbociclib (MESH:C500026)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12986363/full.md

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Source: https://tomesphere.com/paper/PMC12986363