Lead Time and Overdiagnosis in Prostate-Specific Antigen Screening: Importance of Methods and Context

被引:599
作者
Draisma, Gerrit [1 ]
Etzioni, Ruth [2 ]
Tsodikov, Alex [3 ]
Mariotto, Angela [4 ]
Wever, Elisabeth [1 ]
Gulati, Roman [2 ]
Feuer, Eric [4 ]
de Koning, Harry [1 ]
机构
[1] Univ Med Ctr, Erasmus MC, Dept Publ Hlth, NL-3000 CA Rotterdam, Netherlands
[2] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA
[3] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[4] NCI, Div Canc Control & Populat Sci, Bethesda, MD 20892 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2009年 / 101卷 / 06期
关键词
CANCER INCIDENCE; POPULATION-MODEL; MEN; PSA; MORTALITY; DIAGNOSIS; DISEASE; TRENDS; LUNG; SIZE;
D O I
10.1093/jnci/djp001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The time by which prostate-specific antigen (PSA) screening advances prostate cancer diagnosis, called the lead time, has been reported by several studies, but results have varied widely, with mean lead times ranging from 3 to 12 years. A quantity that is closely linked with the lead time is the overdiagnosis frequency, which is the fraction of screen-detected cancers that would not have been diagnosed in the absence of screening. Reported overdiagnosis estimates have also been variable, ranging from 25% to greater than 80% of screen-detected cancers. Methods We used three independently developed mathematical models of prostate cancer progression and detection that were calibrated to incidence data from the Surveillance, Epidemiology, and End Results program to estimate lead times and the fraction of overdiagnosed cancers due to PSA screening among US men aged 54-80 years in 1985-2000. Lead times were estimated by use of three definitions. We also compared US and earlier estimates from the Rotterdam section of the European Randomized Study of Screening for Prostate Cancer (ERSPC) that were calculated by use of a microsimulation screening analysis (MISCAN) model. Results The models yielded similar estimates for each definition of lead time, but estimates differed across definitions. Among screen-detected cancers that would have been diagnosed in the patients' lifetimes, the estimated mean lead time ranged from 5.4 to 6.9 years across models, and overdiagnosis ranged from 23% to 42% of all screen-detected cancers. The original MISCAN model fitted to ERSPC Rotterdam data predicted a mean lead time of 7.9 years and an overdiagnosis estimate of 66%; in the model that was calibrated to the US data, these were 6.9 years and 42%, respectively. Conclusion The precise definition and the population used to estimate lead time and overdiagnosis can be important drivers of study results and should be clearly specified.
引用
收藏
页码:374 / 383
页数:10
相关论文
共 39 条
[1]   Competing risk analysis of men aged 55 to 74 years at diagnosis managed conservatively for clinically localized prostate cancer [J].
Albertsen, PC ;
Hanley, JA ;
Gleason, DF ;
Barry, MJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (11) :975-980
[2]  
[Anonymous], CANC FACTS FIG 2007
[3]  
[Anonymous], NAT HLTH INT SURV 20
[4]   Lead-time in prostate cancer screening (Finland) [J].
Auvinen, A ;
Määttänen, L ;
Stenman, UH ;
Tammela, T ;
Rannikko, S ;
Aro, J ;
Juusela, H ;
Hakama, M .
CANCER CAUSES & CONTROL, 2002, 13 (03) :279-285
[5]   Modeling cancer detection: tumor size as a source of information on unobservable stages of carcinogenesis [J].
Bartoszynski, R ;
Edler, L ;
Hanin, L ;
Kopp-Schneider, A ;
Pavlova, L ;
Tsodikov, A ;
Zorin, A ;
Yakovlev, AY .
MATHEMATICAL BIOSCIENCES, 2001, 171 (02) :113-142
[6]   SIMPLIFIED MODELS OF SCREENING FOR CHRONIC DISEASE - ESTIMATION PROCEDURES FROM MASS-SCREENING PROGRAMS [J].
DAY, NE ;
WALTER, SD .
BIOMETRICS, 1984, 40 (01) :1-14
[7]   Prostate cancer mortality reduction by screening:: Power and time frame with complete enrollment in the European Randomised Screening for Prostate Cancer (ERSPC) trial [J].
de Koning, HJ ;
Liem, MK ;
Baan, CA ;
Boer, R ;
Schröder, FH ;
Alexander, FE .
INTERNATIONAL JOURNAL OF CANCER, 2002, 98 (02) :268-273
[8]   Lead times and overdetection due to prostate-specific antigen screening:: Estimates from the European randomized study of screening for prostate cancer [J].
Draisma, G ;
Boer, R ;
Otto, SJ ;
van der Cruijsen, IW ;
Damhuis, RAM ;
Schröder, FH ;
de Koning, HJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (12) :868-878
[9]   MISCAN: estimating lead-time and over-detection by simulation [J].
Draisma, G ;
De Koning, HJ .
BJU INTERNATIONAL, 2003, 92 :106-111
[10]   Gleason score, age and screening:: Modeling dedifferentiation in prostate cancer [J].
Draisma, Gerrit ;
Postma, Renske ;
Schroder, Fritz H. ;
van der Kwast, Theo H. ;
de Koning, Harry J. .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (10) :2366-2371