drugset / Trial / NCT01309607

Study of Preoperative Weekly Paclitaxel and Carboplatin With Lapatinib (Tykerb®) in Patients With ErbB2-Positive Stage I-III Breast Cancer

NCT01309607 ↗

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of weekly paclitaxel and carboplatin, in combination with lapatinib, in the neoadjuvant treatment of non-metastatic erbB2-positive breast cancer. Secondary objectives include: * To determine the safety and tolerability of weekly paclitaxel and carboplatin, combined with lapatinib, in an Asian population * To determine breast conservation rates following neoadjuvant paclitaxel/ carboplatin/ lapatinib * To determine clinical response rates and relapse-free survival of patients treated with neoadjuvant paclitaxel/ carboplatin/ lapatinib * To identify predictive tumour biomarkers for pathologic complete response The investigators hypothesize that pathologic complete response rates will be improved from 15% to 35% with the neoadjuvant regimen of carboplatin/ paclitaxel/ lapatinib compared to standard chemotherapy alone in HER2 positive early stage breast cancers.

Timeline

Start
2011-04
Primary completion
2014-12
Completion
2015-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 2 unknown —
Subject Lapatinib Small molecule 750 mg —
Subject Paclitaxel Small molecule 80 mg/m2 —