Docetaxel and cisplatin combination chemotherapy in metastatic breast cancer patients with previous exposure to anthracyclines

Breast. 2005 Aug;14(4):304-9. doi: 10.1016/j.breast.2005.02.006. Epub 2005 Apr 18.

Abstract

We evaluated the efficacy and safety of the combination of docetaxel and cisplatin in metastatic breast cancer (MBC) patients previously treated with anthracycline-containing regimens. Between June 1999 and December 2002, 50 female MBC patients (median age 43 years; range 29-64) received docetaxel 75 mg/m(2) and cisplatin 75 mg/m(2) on day 1 of each 4-week cycle. A total of 226 cycles (median four cycles per patient) were administered as first-line (23 patients) or second-line (27 patients) treatment. Five patients (10%) achieved a complete response (CR) and 15 (30%) had partial responses (PR), giving an overall response rate of 40% (95% CI, 26.4 approximately 53.6%). The median duration of response was 6.1 months (range, 2.3 approximately 29.2(+) months). With a median follow-up of 15.9 months, median time to progression was 6.2 months (range 1 approximately 22.5(+) months). Toxicities included grades III and IV neutropenia in nine (18%) and ten (20%) patients, respectively, and febrile neutropenia in seven patients (14%). In conclusion, our data show that docetaxel plus cisplatin is effective with the manageable toxicity profile in MBC patients previously treated with anthracyclines.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology*
  • Cisplatin / administration & dosage
  • Disease Progression
  • Docetaxel
  • Female
  • Humans
  • Middle Aged
  • Neoplasm Metastasis*
  • Neutropenia / chemically induced
  • Survival Analysis
  • Taxoids / administration & dosage
  • Treatment Outcome

Substances

  • Taxoids
  • Docetaxel
  • Cisplatin