Definitions of biochemical failure in prostate cancer following radiation therapy

Int J Radiat Oncol Biol Phys. 2001 Aug 1;50(5):1212-9. doi: 10.1016/s0360-3016(01)01571-1.

Abstract

Purpose: The American Society for Therapeutic Radiology and Oncology (ASTRO) published a consensus panel definition of biochemical failure following radiation therapy for prostate cancer. In this paper, we develop a series of alternative definitions of biochemical failure. Using data from 688 patients, we evaluated the sensitivity and specificity of the various definitions, with respect to a defined "clinically meaningful" outcome.

Methods and materials: The ASTRO definition of biochemical failure requires 3 consecutive rises in prostate-specific antigen (PSA). We considered several modifications to the standard definition: to require PSA rises of a certain magnitude, to consider 2 instead of 3 rises, to require the final PSA value to be greater than a fixed cutoff level, and to define biochemical failure based on the slope of PSA over 1, 1.5, or 2 years. A clinically meaningful failure is defined as local recurrence, distant metastases, initiation of unplanned hormonal therapy, unplanned radical prostatectomy, or a PSA > 25 later than 6 months after radiation.

Results: Requiring the final PSA in a series of consecutive rises to be larger than 1.5 ng/mL increased the specificity of biochemical failure. For a fixed specificity, defining biochemical failure based on 2 consecutive rises, or the slope over the last year, could increase the sensitivity by up to approximately 20%, compared to the ASTRO definition. Using a rule based on the slope over the previous year or 2 rises leads to a slightly earlier detection of biochemical failure than does the ASTRO definition. Even with the best rule, only approximately 20% of true failures are biochemically detected more than 1 year before the clinically meaningful event time.

Conclusion: There is potential for improvement in the ASTRO consensus definition of biochemical failure. Further research is needed, in studies with long follow-up times, to evaluate the relationship between various definitions of biochemical failure and true clinical outcome.

Publication types

  • Evaluation Study

MeSH terms

  • Adenocarcinoma / blood
  • Adenocarcinoma / radiotherapy*
  • Aged
  • Biomarkers, Tumor / blood*
  • Combined Modality Therapy / statistics & numerical data
  • Endpoint Determination
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Metastasis
  • Neoplasm Proteins / blood*
  • Neoplasm Recurrence, Local / epidemiology
  • Predictive Value of Tests
  • Prostate-Specific Antigen / blood*
  • Prostatic Neoplasms / blood
  • Prostatic Neoplasms / radiotherapy*
  • ROC Curve
  • Radiotherapy, Conformal*
  • Salvage Therapy / statistics & numerical data
  • Sensitivity and Specificity
  • Treatment Failure

Substances

  • Biomarkers, Tumor
  • Neoplasm Proteins
  • Prostate-Specific Antigen