Clinical efficacy and safety of front-line CDK4/6 inhibitor therapy in HR+/HER2- advanced breast cancer patients with visceral metastases: A retrospective study.

e13074 Background: The introduction of CDK4/6 inhibitors (CDK4/6i) has significantly improved the prognosis of patients with hormone receptor-positive, HER2-negative metastatic breast cancer (HR+/HER2- MBC). Despite these advances, many HR+/HER2- MBC patients still experience disease progression, particularly those with visceral metastases or endocrine resistance. Managing these high-risk subgroups remains a critical challenge in improving patient outcomes. Methods: This single-center, retrospective real-world study included 244 HR+/HER2- MBC patients with visceral metastases, who received frontline (1st-2nd line) CDK4/6i combined with endocrine therapy (ET) between January 2022 and August 2024. Progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and safety were evaluated. Results: The overall mPFS was 29.4 months (95% CI: 22.2-37.0 months), with an ORR of 48.8% and a DCR of 96.3%. Subgroup analysis showed better prognosis in patients with lung metastases (mPFS = 42.1 months). Multivariate analysis confirmed adjuvant chemotherapy as an independent prognostic risk factor and demonstrated that CDK4/6i combined with exemestane significantly reduced the risk of disease progression or death (HR = 0.475, P = 0.017). Additionally, both endocrine-sensitive and endocrine-resistant patients showed therapeutic response to CDK4/6i combined with ET. Patients receiving sequential chemotherapy followed by CDK4/6i also achieved favorable clinical benefit. Hematologic toxicity was the most common adverse events (AEs), but overall safety was manageable. Conclusions: This study provides valuable real-world evidence on the efficacy of CDK4/6i combined with ET in HR+/HER2- MBC patients with visceral metastases, with or without endocrine resistance. Future research could explore optimizing ET selection with CDK4/6i and improving AE management to support better therapeutic outcomes.

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Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e13074
Primary Topic
Advanced Breast Cancer Therapies
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article
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article

Clinical efficacy and safety of front-line CDK4/6 inhibitor therapy in HR+/HER2- advanced breast cancer patients with visceral metastases: A retrospective study.

Xiuwen Guan, Wenna Wang, Peng Yuan, Maiyue He et al.
1 links
Journal of Clinical Oncology
Advanced Breast Cancer Therapies
article

Clinical efficacy and safety of front-line CDK4/6 inhibitor therapy in HR+/HER2- advanced breast cancer patients with visceral metastases: A retrospective study.

Xiuwen Guan, Wenna Wang, Peng Yuan, Maiyue He, Mingxia Jiang, Nilupai Abudureheiyimu, Qiao Li, Qi Zhao, Mengqi Zhang, Xu B, Pin Zhang, Jiaxuan Liu, Shihan Zhou, Fei Ma
article en

Abstract

e13074 Background: The introduction of CDK4/6 inhibitors (CDK4/6i) has significantly improved the prognosis of patients with hormone receptor-positive, HER2-negative metastatic breast cancer (HR+/HER2- MBC). Despite these advances, many HR+/HER2- MBC patients still experience disease progression, particularly those with visceral metastases or endocrine resistance. Managing these high-risk subgroups remains a critical challenge in improving patient outcomes. Methods: This single-center, retrospective real-world study included 244 HR+/HER2- MBC patients with visceral metastases, who received frontline (1st-2nd line) CDK4/6i combined with endocrine therapy (ET) between January 2022 and August 2024. Progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and safety were evaluated. Results: The overall mPFS was 29.4 months (95% CI: 22.2-37.0 months), with an ORR of 48.8% and a DCR of 96.3%. Subgroup analysis showed better prognosis in patients with lung metastases (mPFS = 42.1 months). Multivariate analysis confirmed adjuvant chemotherapy as an independent prognostic risk factor and demonstrated that CDK4/6i combined with exemestane significantly reduced the risk of disease progression or death (HR = 0.475, P = 0.017). Additionally, both endocrine-sensitive and endocrine-resistant patients showed therapeutic response to CDK4/6i combined with ET. Patients receiving sequential chemotherapy followed by CDK4/6i also achieved favorable clinical benefit. Hematologic toxicity was the most common adverse events (AEs), but overall safety was manageable. Conclusions: This study provides valuable real-world evidence on the efficacy of CDK4/6i combined with ET in HR+/HER2- MBC patients with visceral metastases, with or without endocrine resistance. Future research could explore optimizing ET selection with CDK4/6i and improving AE management to support better therapeutic outcomes.

Journal of Clinical OncologyVol. 43(16_suppl)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN)
Openalex Percentile: Top 80%
Advanced Breast Cancer Therapies
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