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Capecitabine Plus Radiotherapy for Local Relapse Breast Cancer With Negative Her2 Tumours

Breast Cancer Clinical Trial

Official title:
Multicenter Phase IV.II Trial, for the Administration of Capecitabine Simultaneous to Radiotherapy for Local Relapse Breast Cancer Patients With Negative Her2 Tumours

Clinical Trial Summary

This is a prospective, open-label, multicenter phase IV.II study. Patients with local relapse breast cancer will receive radiotherapy concomitant to the administration of capecitabine.

Clinical Trial Description

Total dose of radiotherapy will be 50 Gy administered in daily session of 200 centigray (cGy). Radiotherapy treatment will not be longer than 6 weeks.

All patients will receive 1650 mg/m2 by mouth, per day (825 mg/m2 twice a day (p.o. bid) for 35 days.

Tissue samples must be analysed to determinate the human epidermal growth factor receptor-2 (HER2) by fluorescent in situ hybridization (FISH) technical. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00434941
Study type Interventional
Source Spanish Breast Cancer Research Group
Contact
Status Terminated
Phase Phase 2
Start date September 2007
Completion date January 2009
View Details
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