Metastatic disease of screen-detected prostate cancer -: Characteristics at diagnosis

被引:0
|
作者
Roemeling, Stijn
Kranse, Ries
Vis, Andre N.
Gosselaar, Claartje
van der Kwast, Theo H.
Schroder, Fritz H.
机构
[1] Univ Med Ctr, Dept Urol, Erasmus MC, NL-3000 CA Rotterdam, Netherlands
[2] Ctr Comprehens Canc, Rotterdam, Netherlands
[3] Univ Med Ctr, Dept Pathol, Erasmus MC, Rotterdam, Netherlands
[4] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
关键词
prostate cancer; mass screening; neoplasm metastasis; prognostic factors; survival;
D O I
10.1002/cncr.22374
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Screening for prostate cancer has not only led to a stage migration, but also to a higher incidence of the disease. A decrease in mortality has occurred in several countries during the same time period. Risk stratification of screen-detected cancers at diagnosis has become more important for the anticipation and interpretation of changing incidence/mortality ratios. METHODS. From 1993 to 1998, 633 men were diagnosed with nonmetastatic prostate cancer in the prevalence screen of the Rotterdam section of the European Randomized study of Screening for Prostate Cancer (ERSPC). The characteristics at diagnosis of men who developed metastatic disease were compared with men without evidence of metastases during follow-tip. RESULTS. During the median follow-tip of 7.5 years, 41 men developed metastatic disease. After 10 years the metastasis-free survival rate was 89.6%, the overall survival 64.7%. In a Cox-model 2logPSA (prostate-specific antigen), biopsy Gleason score and the number of biopsy cores with prostate cancer were independent predictors for the development of metastases; the latter only predicted metastases that presented within 60 months of follow-up. CONCLUSION. The metastasis-free survival of men with prostate cancer detected in a prevalence screening was very high. Whether this was related to the beneficial effects of screening or to overdiagnosis due to screening (or both) remains unclear. The prognostic factors known for clinically diagnosed disease also hold for screen-detected disease.
引用
收藏
页码:2779 / 2785
页数:7
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