Long-lasting control of triple-negative metastatic breast cancer with the novel drug combination ixabepilone and capecitabine--case report

Onkologie. 2010;33(1-2):53-6. doi: 10.1159/000264615. Epub 2010 Jan 5.

Abstract

Background: The optimal duration of ixabepilone and capecitabine chemotherapy combination is currently not known and will most likely be patient-specific based on efficacy, toxicity, quality of life, and patient preference.

Case report: We report an extremely long duration of chemotherapy with ixabepilone and capecitabine (42 cycles) in a patient with triple-negative metastatic breast cancer previously treated with anthracyclines and taxanes. Partial remission was achieved, and acceptable toxicity was observed.

Conclusions: This report adds to the pool of knowledge regarding the use of this important new metastatic breast cancer regimen, especially with respect to the optimal duration of its use.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Biomarkers, Tumor / genetics
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Capecitabine
  • Carcinoma, Ductal / drug therapy
  • Carcinoma, Ductal / genetics
  • Carcinoma, Ductal / secondary*
  • Carcinoma, Papillary / drug therapy
  • Carcinoma, Papillary / genetics
  • Carcinoma, Papillary / secondary*
  • Combined Modality Therapy
  • Deoxycytidine / administration & dosage
  • Deoxycytidine / adverse effects
  • Deoxycytidine / analogs & derivatives
  • Disease Progression
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Epothilones / administration & dosage
  • Epothilones / adverse effects
  • Female
  • Fluorouracil / administration & dosage
  • Fluorouracil / adverse effects
  • Fluorouracil / analogs & derivatives
  • Follow-Up Studies
  • Humans
  • Long-Term Care
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / secondary*
  • Middle Aged
  • Neoplasms, Second Primary / drug therapy*
  • Neoplasms, Second Primary / genetics
  • Randomized Controlled Trials as Topic
  • Receptor, ErbB-2 / genetics
  • Receptors, Estrogen / genetics
  • Receptors, Progesterone / genetics

Substances

  • Biomarkers, Tumor
  • Epothilones
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Deoxycytidine
  • Capecitabine
  • Receptor, ErbB-2
  • ixabepilone
  • Fluorouracil