# A real-world study of palbociclib plus endocrine therapy with or without a short course chemotherapy in the first-line treatment of HR-positive HER2-negative metastatic breast cancer

**Authors:** Xiangjun Li, Yuhua Song, Meng Lv, Yongmei Wang, Xueqiang Gao, Tianyi Ma, Teng Ma, Changgen Liu, Xinyi Sun, Haibo Wang, Yan Mao

PMC · DOI: 10.3389/fonc.2025.1512496 · 2025-07-09

## TL;DR

This study compares starting palbociclib plus hormone therapy versus using it after chemotherapy for metastatic breast cancer, finding similar short-term outcomes but better long-term survival with the initial treatment.

## Contribution

The study provides real-world evidence that early use of palbociclib plus endocrine therapy improves overall survival in metastatic breast cancer patients.

## Key findings

- No significant difference in progression-free survival between initial and post-chemotherapy treatment groups.
- Initial palbociclib plus endocrine therapy was significantly correlated with improved overall survival.
- Disease control rates were high in both groups, with group B achieving 100%.

## Abstract

To investigate the efficacy of palbociclib plus endocrine therapy (ET) as the initial treatment compared with post-chemotherapy maintenance therapy in the first-line treatment of hormone receptor-positive (HR-positive), human epidermal growth factor receptor 2-negative (HER2-negative) metastatic breast cancer (MBC).

A total of 110 patients with HR-positive HER2-negative MBC were enrolled in this study between 2018 and 2023. Progression-free-survivals (PFS) and Overall Survival (OS) of palbociclib plus ET as the initial treatment (group A, n:78) or as post-chemotherapy maintenance therapy (group B, n:32) were calculated. We used the multivariable Cox model to investigate the relationship between each factor and prognosis and performed subgroup analysis.

The median duration of follow-up across the cohort was 45.3 months (95% CI, 42.7 to 50.9 months) in all patients. Statistical analysis revealed no significant difference in PFS between the two groups (p=0.21). 50% was the objective response rate (ORR) for both groups. The disease control rate (DCR) for group A was 95.1% (95%CI 0.88 to 0.98), and for group B, it was 100% (95% CI 0.89 to 1.00). Multivariate Cox regression analysis indicated that the initial administration of palbociclib plus ET was significantly correlated with improved OS (Hazard Ratio [HR] = 0.36, 95% CI, 1.20 to 11.14, p < 0.05).

This real-world study revealed that the commencement of therapy with palbociclib in synergy with ET was preferable to effective chemotherapy followed by palbociclib plus ET.

## Linked entities

- **Chemicals:** palbociclib (PubChem CID 5330286)

## Full-text entities

- **Genes:** NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** MBC (MESH:D001943)
- **Chemicals:** palbociclib (MESH:C500026)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12283718/full.md

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Source: https://tomesphere.com/paper/PMC12283718