Prognostic value of neuroendocrine serum markers and PSA in irradiated patients with pN0 localized prostate cancer

Prostate. 2001 Feb 1;46(2):126-33. doi: 10.1002/1097-0045(20010201)46:2<126::aid-pros1016>3.0.co;2-7.

Abstract

Background: The prognosis of patients with localized prostate cancer depends on clinical stage, histological grade, and pretreatment prostate-specific antigen (PSA). We evaluated the additional prognostic impact of serum levels of neuron-specific enolase (NSE) and chromograninA (CgA) after curative radiotherapy and the importance of serum PSA, analyzed 3 months after irradiation.

Methods: From 1988 to 1995, 161 patients with localized T1-4, pN0M0, prostate adenocarcinoma were treated with external radiation (66Gy, 2Gy/5 fractions per week). Frozen serum samples were assessed for CgA, NSE, and PSA before and 3 months after radiotherapy. CgA was analyzed in only 100 patients. NSE and CgA were determined by a immunometric assay. Total PSA was measured by a time-resolved fluoro-immunometric assay.

Results: Prior to radiotherapy CgA was elevated in 16 of 100 patients, and NSE was elevated in 33 of the 161 patients. There was no association between grade, T category or pretreatment PSA and the levels of neuroendocrine markers. Pretreatment-elevated serum NSE, but not initial CgA, identified patients with an unfavorable prognosis. A < 50% reduction of PSA 3 months after radiotherapy was associated with decreased failure-free 10 years urvival. Multivariate analysis demonstrated an increased risk of failure for patients with elevated pretreatment NSE and PSA values, T3 category, and decline of PSA less than 50% 3 months after radiotherapy. The presence of none or several risk factors (1-4) defined clearly separable groups.

Conclusions: Together with T category and pretreatment serum PSA values, serum NSE values before radiotherapy and decrease of serum PSA 3 months after radiotherapy represent easily assessable prognostic parameters in patients undergoing curative radiation treatment for prostate cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / blood*
  • Adenocarcinoma / immunology
  • Adenocarcinoma / radiotherapy
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / blood*
  • Chromogranin A
  • Chromogranins / blood*
  • Disease-Free Survival
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Staging
  • Phosphopyruvate Hydratase / blood*
  • Prostate-Specific Antigen / blood*
  • Prostatic Neoplasms / blood
  • Prostatic Neoplasms / immunology
  • Prostatic Neoplasms / pathology
  • Prostatic Neoplasms / radiotherapy

Substances

  • Biomarkers, Tumor
  • Chromogranin A
  • Chromogranins
  • Prostate-Specific Antigen
  • Phosphopyruvate Hydratase