Phase II Trial of Eribulin in Patients With Metastatic Hormone Refractory Prostate Cancer: A Trial of the ECOG-ACRIN

Mark N Stein1, Yu-Hui Chen2, Michael A Carducci3

  • 1Columbia University Medical Center, New York, NY.

Abstract

Insights

Eribulin mesylate showed limited efficacy in treating metastatic castration-resistant prostate cancer (CRPC). The study concluded that eribulin is not suitable for further investigation in this patient population.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Eribulin mesylate is a novel synthetic analog of halichondrin B.
  • It functions as a tubulin-binding agent, inhibiting cancer cell proliferation.
  • Demonstrates potent anti-cancer activity at low nanomolar concentrations.

Purpose of the Study:

  • To evaluate the efficacy of eribulin mesylate in patients with metastatic castration-resistant prostate cancer (CRPC).
  • To assess response rates and progression-free survival in different patient strata.
  • To determine the safety and tolerability of eribulin in this population.

Main Methods:

  • A multicenter ECOG trial treated patients with progressive metastatic CRPC.
  • Patients received eribulin 1.4 mg/m² intravenously on days 1 and 8 of a 21-day cycle.
  • The study stratified patients into chemotherapy-naive, prior-taxane, or two-prior-cytotoxic chemotherapy arms.

Main Results:

  • Confirmed PSA response rates were 29% (chemotherapy-naive), 10% (prior-taxane), and 4% (two-prior-chemotherapy).
  • Median progression-free survival ranged from 2.3 to 3.7 months across strata.
  • Common toxicities included fatigue, neuropathy, alopecia, nausea, anorexia, and hematological changes.

Conclusions:

  • Eribulin did not demonstrate adequate activity in chemotherapy-naive or pretreated metastatic CRPC patients.
  • The study concluded that eribulin is not supported for further investigation in this setting.
  • The observed efficacy did not meet prespecified study endpoints.

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