TY - JOUR
T1 - Pyrotinib or placebo in combination with trastuzumab and docetaxel for HER2 positive metastatic breast cancer
T2 - long term survival results from randomised phase 3 PHILA trial
AU - Ma, Fei
AU - Yan, Min
AU - Li, Wei
AU - Ouyang, Quchang
AU - Tong, Zhongsheng
AU - Teng, Yuee
AU - Wang, Yongsheng
AU - Wang, Shusen
AU - Geng, Cuizhi
AU - Luo, Ting
AU - Zhong, Jincai
AU - Zhang, Qingyuan
AU - Liu, Qiang
AU - Zeng, Xiaohua
AU - Sun, Tao
AU - Mo, Qinguo
AU - Zhou, Shoubing
AU - Li, Peidong
AU - Cheng, Jing
AU - Wang, Xiaojia
AU - Nie, Jianyun
AU - Yang, Jin
AU - Wu, Xinhong
AU - Wang, Xinshuai
AU - Li, Huiping
AU - Yao, Guangyu
AU - Fan, Yang
AU - Lin, Jiaman
AU - Zhu, Xiaoyu
AU - Xu, Binghe
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
PY - 2026/1/2
Y1 - 2026/1/2
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105033559149
U2 - 10.1136/bmj-2025-087259
DO - 10.1136/bmj-2025-087259
M3 - 文章
C2 - 41839514
AN - SCOPUS:105033559149
SN - 1756-1833
VL - 392
JO - BMJ (Online)
JF - BMJ (Online)
ER -