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Efficacy and safety of neoadjuvant treatment of trastuzumab and pyrotinib plus dalpiciclib in HR-negative/HER2-positive breast cancer: an exploratory, open-label phase II study.

International journal of surgery (London, England) 2026 Vol.112(1) p. 865-872

Xiao Z, Chen F, Liao L, Luo S, Liu X, Liu X, Xu T, Hu Y, Luo N, Wang W, Cao J, Wang K, Zhou H, Ding N, Li Y, Huang J, Wang S

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[BACKGROUND] To evaluate the efficacy and safety of a chemotherapy-free regimen consisting of monoclonal antibody trastuzumab, tyrosine kinase inhibitor pyrotinib, and CDK4/6 inhibitor dalpiciclib in

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 95% CI 45.5-78.1
  • 추적기간 20 months

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APA Xiao Z, Chen F, et al. (2026). Efficacy and safety of neoadjuvant treatment of trastuzumab and pyrotinib plus dalpiciclib in HR-negative/HER2-positive breast cancer: an exploratory, open-label phase II study.. International journal of surgery (London, England), 112(1), 865-872. https://doi.org/10.1097/JS9.0000000000003328
MLA Xiao Z, et al.. "Efficacy and safety of neoadjuvant treatment of trastuzumab and pyrotinib plus dalpiciclib in HR-negative/HER2-positive breast cancer: an exploratory, open-label phase II study.." International journal of surgery (London, England), vol. 112, no. 1, 2026, pp. 865-872.
PMID 40968745

Abstract

[BACKGROUND] To evaluate the efficacy and safety of a chemotherapy-free regimen consisting of monoclonal antibody trastuzumab, tyrosine kinase inhibitor pyrotinib, and CDK4/6 inhibitor dalpiciclib in patients with hormone receptor-negative/HER2-positive (HR-HER2+) early breast cancer (EBC).

[MATERIALS AND METHODS] This open-label, single-arm, phase II study was designed using the Simon two-stage method (Registration Number: Chi-CTR-2200060748). Patients with operable HR-HER2+ EBC (T1-3 and N0-2) were enrolled. Eligible patients received trastuzumab (HLX02, 8 mg/kg loading dose, followed by 6 mg/kg every 3 weeks intravenously), pyrotinib (400 mg daily orally), and dalpiciclib (125 mg daily orally for 3 weeks, followed by 1 week off) for 16 weeks. Surgery was performed 3-6 weeks after the completion of drug treatment. The primary endpoint was total pathological complete response (tpCR, ypT0/Tis, and ypN0) rates at surgery, and secondary endpoints included breast pCR (bpCR) rates (ypT0/Tis), residual cancer burden (RCB), objective response rate (ORR), change of Ki-67 scores, survival, and safety.

[RESULTS] Between June 2022 and June 2024, a total of 34 patients with a median age of 55 years (range: 35-67) were enrolled. Thirty patients received all cycles of treatment and underwent surgery with a median follow-up of 20 months. The tpCR was achieved in 19 patients (63.3%; 95% CI, 45.5-78.1%). The bpCR was 66.7% (20/30). The number of patients with RCB-0 or RCB-I was 22 (73.3%). The most common Grade 3 treatment-related adverse events were diarrhea (50.0%), neutropenia (20.6%), and leukopenia (17.7%). No Grade 4 events or treatment-related deaths occurred.

[CONCLUSION] In patients with HR-HER2+ EBC, the neoadjuvant therapy with trastuzumab, pyrotinib, and dalpiciclib has promising activity and manageable toxicity. Further investigation is needed.

MeSH Terms

Humans; Female; Breast Neoplasms; Trastuzumab; Middle Aged; Neoadjuvant Therapy; Adult; Acrylamides; Aged; Erb-b2 Receptor Tyrosine Kinases; Antineoplastic Combined Chemotherapy Protocols; Aminoquinolines; Treatment Outcome; Piperidines; Pyridines; Pyrimidines

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