Breast Cancer Research and Treatment

, Volume 66, Issue 1, pp 83–87

Phase II study of weekly gemcitabine in patients with metastatic breast cancer relapsing or failing both an anthracycline and a taxane

Authors

  • C.H. Smorenburg
    • Department of Medical OncologyRotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
  • M. Bontenbal
    • Department of Medical OncologyRotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
  • C. Seynaeve
    • Department of Medical OncologyRotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
  • C. van Zuylen
    • Department of Medical OncologyRotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
  • G. de Heus
    • Department of Medical OncologyRotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
  • J. Verweij
    • Department of Medical OncologyRotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
  • R. de Wit
    • Department of Medical OncologyRotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam
Article

DOI: 10.1023/A:1010679127390

Cite this article as:
Smorenburg, C., Bontenbal, M., Seynaeve, C. et al. Breast Cancer Res Treat (2001) 66: 83. doi:10.1023/A:1010679127390

Abstract

A phase II study was performed to investigate the efficacy and tolerability of gemcitabine as third-line chemotherapy for patients with metastatic breast cancer, previously treated with both an anthracycline - and taxane-containing regimen. Twenty-three patients were treated with gemcitabine 1200 mg/m2 in a 30-min infusion on day 1, 8 and 15 of a 28 day cycle. Seventy-four percent of the patients had visceral metastases. No complete or partial responses were observed. Six patients (26%) had stable disease with a median duration of 4.0 months. The median time to progression was 1.9 months and the median survival time was 7.8 months. Neutropenia grade 3 and 4 was observed in four patients (18%). Non-hematological toxicity grade 3 included nausea and vomiting in 14%, skin toxicity in 9% and elevation of transaminases in 23% of the patients. Gemcitabine is ineffective as third-line single agent therapy in patients failing anthracycline and taxane treatment for metastatic breast cancer.

breast cancerchemotherapygemcitabinethird-line treatment
Download to read the full article text

Copyright information

© Kluwer Academic Publishers 2001