Phase II trial assessing granulocyte-macrophage-colony stimulating factor, ketoconazole plus mitoxantrone in metastatic castration-resistant prostate cancer progressing after docetaxel treatments

Cancer Invest. 2013 Mar;31(3):177-82. doi: 10.3109/07357907.2013.764564. Epub 2013 Feb 12.

Abstract

Introduction: This study evaluated objective response and safety for the combination of granulocyte macrophage-colony stimulating factor (GM-CSF), ketoconazole, and mitoxantrone in castration-resistant prostate cancer (CRPC) patients who previously failed docetaxel-based chemotherapy.

Methods: Treatment consisted of 400 mg TID ketoconazole, 12 mg/m(2) mitoxantrone every 3 weeks, and 250 μg/m(2) GM-CSF.

Results: Twenty-nine patients were evaluable for response. Median overall survival (OS) for all patients was 18.03 months. Patients with a higher PSA decrease experienced an increased OS and progression-free survival (PFS).

Conclusion: This combination demonstrated significant antitumor activity with reversible toxicity in CRPC patients who previously failed docetaxel-based therapy.

Publication types

  • Clinical Trial, Phase II

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Docetaxel
  • Granulocyte-Macrophage Colony-Stimulating Factor / administration & dosage
  • Humans
  • Ketoconazole / administration & dosage
  • Male
  • Middle Aged
  • Mitoxantrone / administration & dosage
  • Orchiectomy
  • Prostate-Specific Antigen / blood
  • Prostatic Neoplasms / blood
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / mortality
  • Taxoids / administration & dosage

Substances

  • Taxoids
  • Docetaxel
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Mitoxantrone
  • Prostate-Specific Antigen
  • Ketoconazole