drugset / Trial / NCT03080805

Pyrotinib Plus Capecitabine Versus Lapatinib Plus Capecitabine in Patients With HER2+ Metastatic Breast Cancer. (PHOEBE)

NCT03080805 ↗

Phase 3 Unknown 240 enrolled Jiangsu HengRui Medicine Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

Pyrotinib is an oral tyrosine kinase inhibitor targeting both HER-1 and HER-2 receptors. This study is a randomized,open-label,multi-center,active-controlled, parallel design study of the combination of pyrotinib and capecitabine versus Lapatinib plus capecitabine in HER2+ MBC patients, who have prior received taxane and trastuzumab.Patients will be randomized in a 1:1 ratio to one of the following treatment arms.Arm A: pyrotinib (400 mg once daily) + capecitabine (1000 mg/m\^2 twice daily),Arm B: Lapatinib (1250 mg once daily) + capecitabine (1000 mg/m\^2 twice daily).Patients will receive either arm of therapy until disease progression, unacceptable toxicity, or withdrawalof consent.

Timeline

Start
2017-05-03
Primary completion
2019-03-31
Completion
2021-03

Outcome

Met primary endpoint

paper median progression-free survival was significantly longer with pyrotinib plus capecitabine PMID 33581774 ↗

paper than with lapatinib plus capecitabine (6·8 months [5·4-8·1]; hazard ratio 0·39 [95% CI 0·27-0·56]; one-sided p<0·0001). PMID 33581774 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lapatinib Small molecule 1250 mg —
Subject Pyrotinib Small molecule 400 mg Oral
Comparator Capecitabine Small molecule 1000 mg/m2 Oral