The role of the digital rectal examination in subsequent screening visits in the European Randomized Study of Screening for Prostate Cancer (ERSPC), Rotterdam

被引:86
作者
Gosselaar, Claartje [1 ]
Roobol, Monique J. [1 ]
Roemeling, Stijn [1 ]
Schroder, Fritz H. [1 ]
机构
[1] Univ Med Ctr, Erasmus MC, Dept Urol, NL-3000 CA Rotterdam, Netherlands
关键词
digital rectal examination; prostate cancer; screening;
D O I
10.1016/j.eururo.2008.03.104
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: The value of digital rectal examination (DRE) as a screening test for prostate cancer (PC) is controversial in the current prostate-specific antigen (PSA) era. Objectives: To determine (1) the additional value of a suspicious DRE for the detection of PC in men with an elevated PSA level in subsequent screenings and (2) the tumour characteristics of PCs detected in men with a suspicious DRE. Design, setting, participants: Within the screening study, from 1997-2006 men aged 55-75 years were invited for an every 4-yr PSA determination. A PSA level > 3.0 ng/ml prompted a DRE and a transrectal ultrasound (TRUS)-guided, lateralized sextant biopsy. Throughout the three screenings of the ERSPC, Rotterdam, 5040 biopsy sessions were evaluated. Measurements: We deter-mined the positive predictive values (PPVs) of a suspicious DRE and normal DRE, which entailed, respectively, the proportion of PCs detected in men with a suspicious DRE or normal DRE divided by, respectively, all biopsied men with a suspicious DRE or normal DRE. Results and limitations: At initial screening, the PPV of a suspicious DRE, in conjunction with an elevated PSA level, to detect PC was 48.6% compared to 22.4% for men with a normal DRE. Both PPVs decreased in consecutive screens: respectively, 29.9% versus 17.1% (screen 2) and 21.2% versus 18.2% (screen 3). Respectively, 71.0% (p < 0.001), 68.8% (p < 0.001), and 85.7% (p = 0.002) of all PCs with a Gleason score > 7 were detected in men with a suspicious DRE at screens 1, 2, and 3. A limitation is that only biopsied men were evaluated. Conclusions: At initial and subsequent screenings, the chance of having cancer at biopsy was higher in men with a suspicious DRE compared to men with a normal DRE (to a lesser extent in subsequent screenings), and the combination of a PSA level > 3.0 ng/ml with a suspicious DRE resulted in detecting significantly more PCs with Gleason score > 7. DRE may be useful in more selective screening procedures to decrease unnecessary biopsies and overdiagnosis. (C) 2008 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:581 / 588
页数:8
相关论文
共 40 条
[31]   Interval cancers in prostate cancer screening:: Comparing 2- and 4-year screening intervals in the European randomized study of screening for prostate cancer, Gothenburg and Rotterdam [J].
Roobol, Monique J. ;
Grenabo, Anna ;
Schroeder, Fritz H. ;
Hugosson, Jonas .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (17) :1296-1303
[32]   The story of the European Randomized study of screening for prostate cancer [J].
Schröder, FH ;
Denis, LJ ;
Roobol, M .
BJU INTERNATIONAL, 2003, 92 :1-13
[33]   Evaluation of the digital rectal examination as a screening test for prostate cancer [J].
Schroder, FH ;
van der Maas, P ;
Beemsterboer, P ;
Kruger, AB ;
Hoedemaeker, R ;
Rietbergen, J ;
Kranse, R .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (23) :1817-1823
[34]   INTEREXAMINER VARIABILITY OF DIGITAL RECTAL EXAMINATION IN DETECTING PROSTATE-CANCER [J].
SMITH, DS ;
CATALONA, WJ .
UROLOGY, 1995, 45 (01) :70-74
[35]   MAKING THE MOST OUT OF 6 SYSTEMATIC SEXTANT BIOPSIES [J].
STAMEY, TA .
UROLOGY, 1995, 45 (01) :2-12
[36]   Prediction of indolent prostate cancer:: Validation and updating of a prognostic nomogram [J].
Steyerberg, E. W. ;
Roobol, M. J. ;
Kattan, M. W. ;
van der Kwast, T. H. ;
de Koning, H. J. ;
Schroder, F. H. .
JOURNAL OF UROLOGY, 2007, 177 (01) :107-112
[37]   Assessing prostate cancer risk: Results from the prostate cancer prevention trial [J].
Thompson, IM ;
Ankerst, DP ;
Chi, C ;
Goodman, PJ ;
Tangen, CM ;
Lucia, MS ;
Feng, ZD ;
Parnes, HL ;
Coltman, CA .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (08) :529-534
[38]   Tumor characteristics and prognostic factors in two subsequent screening rounds with four-year interval within prostate cancer screening trial, ERSPC Rotterdam [J].
Van Der Cruijsen-Koeter, Ingrid W. ;
Roobol, Monique J. ;
Wildhagen, Mark F. ;
Van Der Kwast, T. H. ;
Kirkels, W. J. ;
Schroeder, Fritz H. .
UROLOGY, 2006, 68 (03) :615-620
[39]   Interval carcinomas in the European Randomized Study of Screening for Prostate Cancer (ERSPC)-Rotterdam [J].
van der Cruijsen-Koeter, IW ;
van der Kwast, TH ;
Schröder, FH .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (19) :1462-1466
[40]   A model for the number of cores per prostate biopsy based on patient age and prostate gland volume [J].
Vashi, AR ;
Wojno, KJ ;
Gillespie, B ;
Oesterling, JE .
JOURNAL OF UROLOGY, 1998, 159 (03) :920-924