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Pyrotinib or placebo in combination with trastuzumab and docetaxel for HER2 positive metastatic breast cancer: long term survival results from randomised phase 3 PHILA trial

  • Fei Ma
  • , Min Yan
  • , Wei Li
  • , Quchang Ouyang
  • , Zhongsheng Tong
  • , Yuee Teng
  • , Yongsheng Wang
  • , Shusen Wang
  • , Cuizhi Geng
  • , Ting Luo
  • , Jincai Zhong
  • , Qingyuan Zhang
  • , Qiang Liu
  • , Xiaohua Zeng
  • , Tao Sun
  • , Qinguo Mo
  • , Shoubing Zhou
  • , Peidong Li
  • , Jing Cheng
  • , Xiaojia Wang
  • Jianyun Nie, Jin Yang, Xinhong Wu, Xinshuai Wang, Huiping Li, Guangyu Yao, Yang Fan, Jiaman Lin, Xiaoyu Zhu, Binghe Xu
  • Chinese Academy of Medical Sciences
  • Zhengzhou University
  • Jilin University
  • Central South University
  • Tianjin Medical University
  • China Medical University
  • Shandong Cancer Hospital
  • Sun Yat-Sen University Cancer Center
  • Hebei Medical University
  • Sichuan University
  • The First Affiliated Hospital of Guangxi Medical University
  • Harbin Medical University
  • Sun Yat-Sen University
  • Chongqing University Cancer Hospital
  • Liaoning Tumor Hospital & Institute
  • Guangxi Medical University
  • The First Affiliated Hospital of University of Science and Technology of China
  • Jilin Cancer Hospital
  • Huazhong University of Science and Technology
  • Zhejiang Cancer Hospital
  • Yunnan Cancer Hospital
  • The First Affiliated Hospital of Xi’an Jiaotong University
  • Hubei Cancer Hospital
  • Henan University of Science and Technology
  • Peking University
  • Southern Medical University
  • Jiangsu Hengrui Medicine

科研成果: 期刊稿件文章同行评审

2 引用 (Scopus)

摘要

AbstractObjectiveTo report updated results of the phase 3 PHILA trial, which evaluated the efficacy and safety of pyrotinib or placebo in combination with trastuzumab and docetaxel in patients with untreated human epidermal growth factor receptor 2 (HER2) positive metastatic breast cancer.DesignMulticentre, double blind, randomised, placebo controlled phase 3 trial.Setting40 centres in China, 6 May 2019 to 17 January 2022.Participants590 female patients with untreated HER2 positive metastatic breast cancer.InterventionsEligible patients were randomly assigned in a 1:1 ratio to receive either the irreversible pan-HER inhibitor pyrotinib (400 mg orally once daily) or placebo, both in combination with intravenous trastuzumab (8 mg/kg for the first cycle, then 6 mg/kg in subsequent cycles) and docetaxel (75 mg/m2) on day 1 of each 21 day treatment cycle.Main outcome measureThe primary endpoint was investigator assessed progression-free survival.Results590 patients were randomised and received treatment (297 in the pyrotinib group and 293 in the placebo group). As of 30 April 2024, during a median follow-up of 35.7 months in the pyrotinib group and 34.3 months in the placebo group, 59 (20%) and 87 (30%) patients died, respectively. Overall survival was longer in the pyrotinib group (hazard ratio 0.64 (95% confidence interval (CI) 0.46 to 0.89); nominal one-sided P=0.004). At end of follow-up, neither group had reached the median overall survival. Improvement in progression-free survival in the pyrotinib group was maintained (22.1 months (95% CI 19.3 to 27.8) v 10.5 months (9.5 to 12.4), hazard ratio 0.44 (95% CI 0.36 to 0.53); nominal one sided P<0.001). Adverse event profiles remained consistent with the interim analysis for type, frequency, and severity. After discontinuation of docetaxel, the overall incidence of adverse events decreased substantially. As of 30 May 2025, with a median follow-up of 45.5 months, the pyrotinib based regimen showed consistent and prolonged survival benefit.ConclusionsThe updated analysis of the phase 3 PHILA trial confirmed the superiority of pyrotinib in combination with trastuzumab and docetaxel over placebo in combination with trastuzumab and docetaxel in sustaining longer progression-free survival and improving overall survival for initial treatment of HER2 positive metastatic breast cancer. The safety profile remained consistent with interim findings, with no new safety signals identified during extended follow-up. This analysis reinforces the efficacy of this dual anti-HER2 (pyrotinib plus trastuzumab) regimen as an effective treatment strategy for this patient population.Trial registrationClinicalTrials.gov NCT03863223.

源语言英语
期刊BMJ (Online)
392
DOI
出版状态已出版 - 2 1月 2026
已对外发布

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  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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