Large-scale randomized prostate cancer screening trials:: Program performances in the European randomized screening for prostate cancer trial and the prostate, lung, colorectal and ovary cancer trial

被引:218
作者
de Koning, HJ
Auvinen, A
Sanchez, AB
da Silva, FC
Ciatto, S
Denis, L
Gohagan, JK
Hakama, M
Hugosson, J
Kranse, R
Nelen, V
Prorok, PC
Schröder, FH
机构
[1] Erasmus Univ, Dept Publ Hlth, NL-3000 DR Rotterdam, Netherlands
[2] Inst Stat Canc Res, Finnish Canc Registry, Helsinki, Finland
[3] Hosp Univ Getafe, Madrid, Spain
[4] Hosp Desterro, Lisbon, Portugal
[5] Ctr Studio & Prevenz Oncol, Dept Diagnost Med Imaging, I-50131 Florence, Italy
[6] Oncol Ctr Antwerp, Antwerp, Belgium
[7] NCI, Early Detect Branch, NIH, Bethesda, MD 20892 USA
[8] Univ Tampere, Dept Publ Hlth, FIN-33101 Tampere, Finland
[9] Sahlgrenska Univ Hosp Ostra, Dept Urol, Gothenburg, Sweden
[10] Rotterdam Canc Registry, Rotterdam, Netherlands
[11] Prov Inst Hyg, Antwerp, Belgium
[12] NCI, Screening Sect, Biometry Branch, NIH, Bethesda, MD 20892 USA
[13] Erasmus Univ, Dept Urol, NL-3000 DR Rotterdam, Netherlands
[14] Acad Hosp Rotterdam, Rotterdam, Netherlands
关键词
prostate cancer screening trials; randomized; controlled trial; PSA;
D O I
10.1002/ijc.1588
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Two large-scale randomized screening trials, the Prostate, Lung, Colorectal and Ovary (PLCO) cancer trial in the USA and the European Randomized Screening for Prostate Cancer (ERSPC) trial in Europe are currently under way, aimed at assessing whether screening reduces prostate cancer mortality. Up to the end of 1998, 102,691 men have been randomized to the intervention arm and 115,322 to the control arm (which represents 83% of the target sample size) from 7 European countries and 10 screening centers in the USA. The principal screening method at all centers is determination of serum prostate-specific antigen (PSA). The PLCO trial and some European centers use also digital rectal examination (DRE) as an ancillary screening test. In the core age group (55-69 years), 3,362 of 32,486 men screened (10%) had a serum PSA concentration of 4 ng/ml or greater, which is 1 cut-off for biopsy (performed in 84%). An additional 6% was referred for further assessment based on other criteria, with much less efficiency. Differences in PSA by country are largely attributable to the age structure of the study population. The mean age-specific PSA levels are lower in the PLCO trial (1.64 ng/ml [in the age group 55-59 years], 1.80 [60-64 years] and 2.18 [65-69 years) than in the ERSPC trial (1.28-1.71 [55-59], 1.75-2.87 [60-64] and 2.48-3.06 [65-69 years]). Detection rates at the first screen in the ERSPC trial range from 11 to 42/1,000 men screened and reflect underlying differences in incidence rates and screening procedures. In centers with consent to randomization design, adherence in the screening arm is 91%, but less than half of the men in the target population are enrolled in the trial. In population-based centers in which men were randomized prior to consent, all eligible subjects are enrolled, but only about two-thirds of the men in the intervention arm undergo screening. Considerable progress has been made in both trials. Enrollment will be completed in 2001. A substantial number of early prostate cancers have been detected. The differences between countries seem to reflect both underlying prostate cancer incidence and screening policy. The trials have the power to show definitive results in 2005-2008. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:237 / 244
页数:8
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