The risk of rapid prostate specific antigen increase in men with baseline prostate specific antigen 2.0 ng/ml or less

被引:9
作者
Ito, K [1 ]
Yamamoto, T [1 ]
Suzuki, K [1 ]
Kurokawa, K [1 ]
Yamanaka, H [1 ]
机构
[1] Gunma Univ, Sch Med, Dept Urol, Maebashi, Gumma 3718511, Japan
关键词
prostate; prostatic neoplasms; prostate-specific antigen; mass screening;
D O I
10.1097/01.ju.0000100109.23348.6b
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
Purpose: We estimated the risk of a rapid prostate specific antigen (PSA) increase in men with a low baseline PSA range of 0.0 to 2.0 ng/ml to investigate the validity of setting a re-screening interval of more than 1 year. Materials and Methods: Between 1988 and 1999, 6,252 men with baseline PSA 2.0 ng/ml or less without suspicious findings on digital rectal examination (DRE) and 7,304 with the same baseline PSA who did not undergo DRE at the time of baseline PSA measurement were rescreened. The risks of a PSA increase to 4.1 to 10.0, 10.1 to 20.0 and greater than 20.0 ng/ml were investigated and stratified by re-screening interval, baseline DRE status, and subdivided baseline PSA ranges of 0.0 to 1.0 and 1.1 to 2.0 ng/ml. Results: A total of 28 cases (0.2% of 13,556) of prostate cancer were detected after an average re-screening interval of 3.6 years. High PSA above 10 ng/ml at diagnosis was noted in 5 patients (18%), including 2 with a great PSA increase to 1,928 and 298 ng/ml at re-screening intervals of 4 and 6 years, respectively. Conclusions: Setting 4 to 5-year re-screening intervals for PSA measurements in men with PSA 1.0 ng/ml. or less can decrease the cost of PSA tests without lowering sensitivity. A re-screening interval for PSA measurement should be set annually for men with PSA 1.1 to 2.0 ng/ml to minimize the risk of missing aggressive cancer.
引用
收藏
页码:656 / 660
页数:5
相关论文
共 11 条
[1]  
Crawford D, 2002, J UROLOGY, V167, P99
[2]   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 [J].
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 .
INTERNATIONAL JOURNAL OF CANCER, 2002, 97 (02) :237-244
[3]   Natural history of PSA increase with and without prostate cancer [J].
Ito, K ;
Yamamato, T ;
Ohi, M ;
Takeuchi, H ;
Kurokawa, K ;
Suzuki, K ;
Yamanaka, H .
UROLOGY, 2003, 62 (01) :64-69
[4]  
Ito K, 2001, CANCER-AM CANCER SOC, V91, P744, DOI 10.1002/1097-0142(20010215)91:4<744::AID-CNCR1060>3.3.CO
[5]  
2-3
[6]  
ITO K, 1999, KITAKANTO MED J, V49, P81
[7]   NATURAL-HISTORY OF CHANGES IN PROSTATE-SPECIFIC ANTIGEN IN EARLY-STAGE PROSTATE-CANCER [J].
PEARSON, JD ;
CARTER, HB .
JOURNAL OF UROLOGY, 1994, 152 (05) :1743-1748
[8]   Design of the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial [J].
Prorok, PC ;
Andriole, GL ;
Bresalier, RS ;
Buys, SS ;
Chia, D ;
Crawford, ED ;
Fogel, R ;
Gelmann, EP ;
Gilbert, F ;
Hasson, MA ;
Hayes, RB ;
Johnson, CC ;
Mandel, JS ;
Oberman, A ;
O'Brien, B ;
Oken, MM ;
Rafla, S ;
Reding, D ;
Rutt, W ;
Weissfeld, JL ;
Yokochi, L ;
Gohagan, JK .
CONTROLLED CLINICAL TRIALS, 2000, 21 (06) :273S-309S
[9]   The European Randomized Study of Screening for Prostate Cancer (ERSBC):: An update [J].
Schröder, FH ;
Kranse, R ;
Rietbergen, J ;
Hoedemaeker, R ;
Kirkels, W .
EUROPEAN UROLOGY, 1999, 35 (5-6) :539-543
[10]   Longitudinal screening for prostate cancer with prostate-specific antigen [J].
Smith, DS ;
Catalona, WJ ;
Herschman, JD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (16) :1309-1315