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Real-World Outcomes of First-Line Palbociclib Plus Endocrine Therapy for HR+/HER2- Metastatic Breast Cancer in Japan:
Keiko Yanagihara1, Masato Yoshida2, Kensaku Awaji2
1Department of Breast Surgery and Oncology, Nippon Medical School Tama-Nagayama Hospital, 1-7-1 Nagayama, Tama-shi, Tokyo, 206-8512, Japan.
Background:
Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors have transformed the management of hormone receptor-positive/HER2-negative (HR+/HER2-) advanced breast cancer, yet evidence for elderly or poor-performance patients remains limited. This study examined real-world outcomes of palbociclib plus endocrine therapy in Asian patients, with additional subgroup analyses by age and performance status.
Methods:
We retrospectively analyzed 46 consecutive Asian patients with recurrent or de novo HR+/HER2- breast cancer treated with first-line palbociclib plus ET between April 2021 and March 2025. The primary endpoint was progression-free survival (PFS). Secondary endpoints included overall response rate (ORR), disease control rate (DCR), and safety. Subgroup analyses were performed by age (<70 vs. ≥70 years) and performance status (PS; 0-1 vs. 2-3).
Results:
The median PFS was 26.6 months (range, 1.4-69.5). Stratified by age, median PFS was 26.9 months in patients <70 years and 26.2 months in those ≥70 years (p = 0.760). By PS, PFS was 26.9 months for PS 0-1 and 17.8 months for PS 2-3 (p = 0.099). ORR was 60.9% and DCR 93.5%; notably, all PS 2-3 patients achieved disease control. Hematologic toxicities were common, with neutropenia (80.4%) and leukopenia (86.7%) predominating, but grade ≥ 3 anemia was rare (2.2%). Elderly patients experienced anemia more frequently, while overall toxicity remained manageable. Dose reductions occurred in 47.8% without loss of efficacy.
Conclusions:
In routine Japanese practice, palbociclib plus ET provided prolonged PFS and high disease control consistent with pivotal trials and international real-world evidence. Importantly, elderly patients tolerated treatment well, and selected PS 2-3 patients also derived clinical benefit. These findings indicate that neither age nor PS alone should preclude the use of palbociclib in carefully monitored real-world patients.
Insights
Palbociclib plus endocrine therapy (ET) shows prolonged progression-free survival (PFS) in Asian patients with advanced hormone receptor-positive/HER2-negative breast cancer. Elderly and poor-performance status patients benefit, with manageable toxicity.
Area of Science:
- Oncology
- Pharmacology
- Clinical Medicine
Background:
- Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors, including palbociclib, have improved outcomes for advanced hormone receptor-positive/HER2-negative (HR+/HER2-) breast cancer.
- Limited real-world data exists for elderly patients or those with poor performance status (PS).
Purpose of the Study:
- To evaluate the real-world effectiveness and safety of palbociclib plus endocrine therapy (ET) in Asian patients with HR+/HER2- advanced breast cancer.
- To conduct subgroup analyses based on age and performance status.
Main Methods:
- Retrospective analysis of 46 Asian patients with HR+/HER2- breast cancer treated with first-line palbociclib plus ET.
- Primary endpoint: progression-free survival (PFS). Secondary endpoints: overall response rate (ORR), disease control rate (DCR), and safety.
- Subgroup analyses by age (<70 vs. ≥70 years) and PS (0-1 vs. 2-3).
Main Results:
- Median PFS was 26.6 months, with no significant difference between age groups (26.9 vs. 26.2 months).
- Patients with PS 0-1 had a median PFS of 26.9 months, compared to 17.8 months for PS 2-3 (p=0.099).
- ORR was 60.9%, DCR was 93.5%, with all PS 2-3 patients achieving disease control. Common toxicities included neutropenia and leukopenia; anemia was rare. Elderly patients had more anemia, but toxicity was manageable.
Conclusions:
- Palbociclib plus ET demonstrates prolonged PFS and high disease control in real-world Asian practice, consistent with clinical trials.
- Elderly patients and selected PS 2-3 patients tolerated treatment well and derived clinical benefit.
- Age and PS should not solely preclude palbociclib use in carefully monitored patients.
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