Staging for prostate cancer - Time to incorporate pretreatment prostate-specific antigen and Gleason score?

被引:13
作者
Roach, Mack, III
Weinberg, Vivian
Sandier, Howard
Thompson, Ian
机构
[1] Univ Calif San Francisco, Ctr Comprehens Canc, Dept Radiat Oncol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, Dept Urol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Ctr Comprehens Canc, Biostat Core, San Francisco, CA 94143 USA
[4] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[5] Univ Texas, Dept Urol, San Antonio, TX 78285 USA
[6] Univ Texas, San Antonio Canc Inst, San Antonio, TX 78285 USA
关键词
prostate cancer; American Joint Committee on Cancer staging system; long-term survival; prostate-specific antigen;
D O I
10.1002/cncr.22403
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The American Joint Committee on Cancer (AJCC) staging system for prostate cancer is based primarily based on clinical tumor (T) classification. In this article, the authors summarize arguments for incorporating additional pretreatment parameters and creating a new staging system for prostate cancer. METHODS. Men with localized prostate cancer who received treatment with external beam radiation alone were analyzed using the 1997 AJCC staging system compared with a system that included pretreatment prostate-specific antigen (pPSA) level and Gleason score (GS). Multivariate analyses using a Cox proportional-hazards model were carried out to evaluate T classification, GS, and pPSA as predictors of overall survival (OS), disease-specific survival (DSS), and freedom from PSA failure (FFPF). RESULTS. Based on pretreatment characteristics in a series of contemporary patients, only 0.6% of patients were classified with AJCC stage I disease, 16.0% were classified with AJCC stage III disease, and 83.4% were classified with AJCC stage 11 disease. Multivariate analyses indicated the independent statistical significance of T classification, GS, and pPSA in predicting OS, DSS, and FFPF (model chi-square value, P <.0001 for each). Using these 3 predictors, subsets of patients who had similar outcomes were combined to provide examples of the insensitivity of the AJCC system for predicting outcomes. Incorporating pPSA and GS allowed the identification of differences in OS, DSS, and FFPF for subsets of patients with AJCC stage 11 disease (P <.0001, P =.005, and P <.0001, respectively). CONCLUSIONS. The current AJCC staging system does not divide contemporary patients with prostate cancer into prognostic subgroups and does not identify patients who have comparable biochemical control and survival. The AJCC staging system for prostate cancer should be changed to incorporate pPSA, GS, and risk stratification.
引用
收藏
页码:213 / 220
页数:8
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