The association between measures of progression and survival in castrate-metastatic prostate cancer

Clin Cancer Res. 2007 Mar 1;13(5):1488-92. doi: 10.1158/1078-0432.CCR-06-1885.

Abstract

Purpose: To explore the association between progression-free survival and overall survival time in patients with castration-resistant prostate cancer treated with microtubule-targeted therapies.

Experimental design: We retrospectively studied patients treated in three trials evaluating a taxane or an epothilone for progressive castration-resistant prostate cancer. Study subjects were 98 patients with bone metastases; 63 of them also had soft tissue lesions. All scans were reviewed independently. Associations of radiographic progression-free survival and prostate-specific antigen (PSA) progression-free survival with survival time were measured using Kendall's tau, adjusted for right censoring. A smoothing procedure was applied to estimate Kendall's tau within each neighborhood of the follow-up process.

Results: The overall associations between progression-free survival time and overall survival time were moderate: 0.4 for radiographic progression-free survival and 0.33 for PSA progression-free survival. The association between radiographic progression-free survival and overall survival was weakest early in the follow-up process, whereas the PSA association was weakest when the progression-free survival-related event (PSA progression, death, or censoring) occurred after 6 months from the start of treatment.

Conclusions: Current measures of progression-free survival time for men with castration-resistant prostate cancer are not strongly concordant with survival time. Factors that attenuate the association include interval censoring and the discontinuation of therapy early in the follow-up due to imaging changes that may not reflect true failure of the treatment. For radiographic progression-free survival, the association may be increased by requiring confirmation of progression with a second scan, as is routinely done when assessing response.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / mortality*
  • Adenocarcinoma / secondary*
  • Androgen Antagonists / therapeutic use
  • Antineoplastic Agents / therapeutic use
  • Antineoplastic Agents, Hormonal / therapeutic use
  • Bone Neoplasms / secondary
  • Clinical Trials as Topic
  • Disease Progression
  • Disease-Free Survival
  • Epothilones / therapeutic use
  • Humans
  • Male
  • Prostate-Specific Antigen / blood
  • Prostatic Neoplasms / drug therapy
  • Prostatic Neoplasms / mortality*
  • Prostatic Neoplasms / secondary*
  • Retrospective Studies
  • Soft Tissue Neoplasms / secondary
  • Survival Rate
  • Taxoids / therapeutic use

Substances

  • Androgen Antagonists
  • Antineoplastic Agents
  • Antineoplastic Agents, Hormonal
  • Epothilones
  • Taxoids
  • Prostate-Specific Antigen