drugset / Trial / NCT01205217

Lapatinib or Trastuzumab Given Prior to Surgery With Chemotherapy in Patients With Early Breast Cancer

NCT01205217 ↗

Phase 2 Withdrawn GlaxoSmithKline
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will test the safety of a drug called lapatinib and how well it works. Lapatinib (also called Tyverb or Tykerb) will be compared with another drug trastuzumab (also called Herceptin). Trastuzumab is an antibody against the HER2 protein. It binds to part of the HER2 protein to stop it working. Clinical trials have found that adding trastuzumab to chemotherapy lowers the rate of cancer recurrence and improves survival in women with HER2 positive breast cancer. Lapatinib also stops the HER2 protein working and may slow or stop cancer cells from growing and may prevent cancer from returning. Lapatinib has been approved in some countries to treat patients with certain types of breast cancer. However lapatinib has not been approved to treat early breast cancer. This study is one of many being carried out involving lapatinib in early breast cancer and these studies are showing that it is a promising treatment. This study will compare lapatinib and trastuzumab. One group of people will take lapatinib and another group will take trastuzumab. The effects of the drugs, both good and bad, will be compared. This study will compare two different durations of HER2 treatment to see if earlier introduction of HER2 treatment is beneficial. The lapatinib group will receive HER2 treatment from the very beginning for 24 weeks prior to surgery and the trastuzumab group will only receive HER2 therapy for 12 weeks prior to surgery.

Timeline

Start
2010-12
Primary completion
2010-12
Completion
2010-12

Outcome

Outcome not reported

Stopped: “Data presented at SABCS 2010 showing that dual blockade is superior to monotherapy”

Drugs

EvaluationDrugModalityDoseRoute
Subject Lapatinib Small molecule 1000 mg Oral
Comparator Trastuzumab Monoclonal antibody 2 mg/kg Intravenous
Background Cyclophosphamide Other / unclassified 600 mg/m2 Intravenous
Background Epirubicin Small molecule 90 mg/m2 Intravenous
Background Paclitaxel Small molecule 80 mg/m2 Intravenous

Indications