Carboplatin and oral etoposide in the treatment of patients with advanced breast cancer refractory to anthracyclines

Tumori. 1993 Dec 31;79(6):389-92. doi: 10.1177/030089169307900603.

Abstract

Aims and background: To determine the efficacy and toxicity of the carboplatin and oral etoposide combination in patients with advanced breast cancer previously treated with anthracyclines.

Methods: Twenty-seven patients were treated with a maximum of 6 cycles of carboplatin (300 mg/m2) and etoposide (200 mg/m2) every 4 weeks. Prior treatment with an anthracycline was given as adjuvant in 17 patients and as first line treatment for advanced disease in 10 patients.

Results: Only 12 (44%) patients completed all 6 cycles of chemotherapy. The median administered dose of carboplatin was 72 mg/m2/week and of etoposide 143 mg/m2/week. Two (7.5%) complete and 4 (15%) partial responses were observed. Both complete responses occurred in patients who received only mitoxantrone-containing adjuvant treatment, and lasted for 36 and 92+ weeks. The main toxicities included anemia (56%), leukopenia (56%), nausea/vomiting (50%) and alopecia (79%).

Conclusions: The combination of carboplatin and oral etoposide is effective and should probably be considered as an alternative therapeutic option for patients with advanced breast cancer refractory to anthracyclines.

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Antibiotics, Antineoplastic / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Carboplatin / administration & dosage
  • Drug Resistance
  • Etoposide / administration & dosage
  • Female
  • Humans
  • Middle Aged
  • Survival Analysis
  • Treatment Outcome

Substances

  • Antibiotics, Antineoplastic
  • Etoposide
  • Carboplatin