PSA markers in prostate cancer detection

被引:78
作者
Gretzer, MB [1 ]
Partin, AW [1 ]
机构
[1] Johns Hopkins Univ Hosp, James Buchanan Brady Urol Inst, Baltimore, MD 21287 USA
关键词
DIGITAL RECTAL EXAMINATION; OPERATING CHARACTERISTIC CURVES; MULTICENTER CLINICAL-TRIAL; ANTIGEN LEVELS; TRANSITION ZONE; 4.0; NG/ML; REFERENCE RANGES; MOLECULAR-FORMS; PRECURSOR FORM; SERUM;
D O I
10.1016/S0094-0143(03)00057-0
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
The prostate-specific antigen (PSA) revolution that has occurred over the previous 2 decades has positively impacted the detection and treatment of men with prostate cancer. Although methods to improve specificity have shown promise (eg, PSA density, age-specific PSA, and PSA velocity), meaningful interpretation has yet to be uniformly accepted within clinical practice. The identification of other molecular forms of PSA within serum has led to a new era in PSA markers. Initial application employing the percentage of free to total PSA has provided improved discrimination between benign and malignant prostatic disease; however, questions remain regarding the ultimate threshold value. The discovery of various free forms of PSA-such as proPSA, benign PSA, and intact PSA-also have introduced the potential for improved specificity in detection. Although early results are encouraging, further evaluation is anticipated. The development of improved methods to detect and measure complexed PSA has demonstrated provocative results, and exhibits the potential to replace PSA as a standard diagnostic test in cancer screening.
引用
收藏
页码:677 / +
页数:11
相关论文
共 96 条
[51]   BPSA, a specific molecular form of free prostate-specific antigen, is found predominantly in the transition zone of patients with nodular benign prostatic hyperplasia [J].
Mikolajczyk, SD ;
Millar, LS ;
Wang, TJ ;
Rittenhouse, HG ;
Wolfert, RL ;
Marks, LS ;
Song, WT ;
Wheeler, TM ;
Slawin, KM .
UROLOGY, 2000, 55 (01) :41-45
[52]  
Morris DL, 1998, J CLIN LAB ANAL, V12, P65
[53]  
Morris DL, 1996, CLIN CHEM, V42, P98
[54]  
NISHIYA M, 1994, CANCER-AM CANCER SOC, V74, P3002, DOI 10.1002/1097-0142(19941201)74:11<3002::AID-CNCR2820741118>3.0.CO
[55]  
2-G
[56]  
Nurmikko P, 2000, CLIN CHEM, V46, P1610
[57]  
Nurmikko P, 2001, CLIN CHEM, V47, P1415
[58]   THE USE OF AGE-SPECIFIC REFERENCE RANGES FOR SERUM PROSTATE-SPECIFIC ANTIGEN IN MEN 60 YEARS OLD OR OLDER [J].
OESTERLING, JE ;
JACOBSEN, SJ ;
COONER, WH .
JOURNAL OF UROLOGY, 1995, 153 (04) :1160-1163
[59]   SERUM PROSTATE-SPECIFIC ANTIGEN IN A COMMUNITY-BASED POPULATION OF HEALTHY-MEN - ESTABLISHMENT OF AGE-SPECIFIC REFERENCE RANGES [J].
OESTERLING, JE ;
JACOBSEN, SJ ;
CHUTE, CG ;
GUESS, HA ;
GIRMAN, CJ ;
PANSER, LA ;
LIEBER, MM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 270 (07) :860-864
[60]   Comparison of two investigative assays for the complexed prostate-specific antigen in total prostate-specific antigen between 4.1 and 10.0 ng/mL [J].
Okegawa, T ;
Noda, H ;
Nutahara, K ;
Higashihara, E .
UROLOGY, 2000, 55 (05) :700-704