Docetaxel in castration-resistant prostate cancer: a single-centre experience

Cancer Invest. 2014 Nov;32(9):445-50. doi: 10.3109/07357907.2014.958233. Epub 2014 Sep 26.

Abstract

We present a single-institution experience reporting the efficacy and safety of docetaxel, administered as first-line chemotherapy, in castration-resistant prostate cancer (CRPC), focusing on patients and treatment parameters. From November 2004 to January 2012, 51 patients received chemotherapy with docetaxel. With a mean follow-up time (from the beginning of CHT) of 1.6 years (range 0.1-5.1 years), 35 patients (68.6%) died for prostate cancer and 48 patients (94.1%) showed progression of the disease. Five factors influenced overall survival: nodal status at diagnosis, neoadjuvant hormonal therapy, number of cycles of docetaxel administered, schedule of docetaxel and ECOG performance status before starting chemotherapy.

Keywords: Bladder; Chemotherapy; Prostate cancer; Therapy.

MeSH terms

  • Administration, Intravenous
  • Aged
  • Aged, 80 and over
  • Anemia / chemically induced
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use
  • Docetaxel
  • Drug Administration Schedule
  • Fatigue / chemically induced
  • Humans
  • Kaplan-Meier Estimate
  • Leukopenia / chemically induced
  • Male
  • Middle Aged
  • Outcome Assessment, Health Care / statistics & numerical data
  • Proportional Hazards Models
  • Prostatic Neoplasms, Castration-Resistant / drug therapy*
  • Taxoids / administration & dosage
  • Taxoids / adverse effects
  • Taxoids / therapeutic use*

Substances

  • Antineoplastic Agents
  • Taxoids
  • Docetaxel