RETRACTED: EPCA-2: A highly specific serum marker for prostate cancer (Retracted Article)

被引:83
作者
Leman, Eddy S.
Cannon, Grant W.
Trock, Bruce J.
Sokoll, Lori J.
Chan, Daniel W.
Mangold, Leslie
Partin, Alan W.
Getzenberg, Robert H. [1 ]
机构
[1] Brady Urol Inst, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21287 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.urology.2007.01.097
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
OBJECTIVES To describe the initial assessment of early prostate cancer antigen (EPCA)-2 as a serum marker for the detection of prostate cancer and to examine its sensitivity and specificity. METHODS Serum samples were obtained from 385 men: those with prostate-specific antigen (PSA) levels less than 2.5 ng/mL, PSA levels of 2.5 ng/mL or greater with negative biopsy findings, benign prostatic hyperplasia, organ-confined prostate cancer, non-organ-confined disease, and prostate cancer with PSA levels less than 2.5 ng/mL. In addition, a diverse group of controls was assessed with an enzyme-linked immunosorbent assay to detect an epitope of the EPCA-2 protein, EPCA-2.22. RESULTS Using a cutoff of 30 ng/mL, the EPCA-2.22 assay had a 92% specificity (95% confidence interval 85% to 96%) for healthy men and men with benign prostatic hyperplasia and 94% sensitivity (95% confidence interval [CI] 93% to 99%) for overall prostate cancer. The specificity for PSA in these selected groups of patients was 65% (95% Cl 55% to 75%). Additionally, EPCA-2.22 was highly accurate in differentiating between localized and extracapsular disease (area under the curve 0.89, 95% CI 0.82 to 0.97, P <0.0001) in contrast to PSA (area under the curve 0.62, 95% C1 0.50 to 0.75, P = 0.05). CONCLUSIONS The results of our study have shown that EPCA-2 is a novel biomarker associated with prostate cancer that has high sensitivity and specificity and accurately differentiates between men with organ-confined and non-organ-confined disease.
引用
收藏
页码:714 / 720
页数:7
相关论文
共 11 条
[1]  
Carter HB., 2002, CAMPBELLS UROLOGY, VEighth, P3055
[2]   Delineation of prognostic biomarkers in prostate cancer [J].
Dhanasekaran, SM ;
Barrette, TR ;
Ghosh, D ;
Shah, R ;
Varambally, S ;
Kurachi, K ;
Pienta, KJ ;
Rubin, MA ;
Chinnaiyan, AM .
NATURE, 2001, 412 (6849) :822-826
[3]  
GETZENBERG RH, 1991, CANCER RES, V51, P6514
[4]   Differential nuclear matrix protein expression in prostate cancers: Correlation with pathologic stage [J].
Lakshmanan, Y ;
Subong, ENP ;
Partin, AW .
JOURNAL OF UROLOGY, 1998, 159 (04) :1354-1358
[5]   Characterization of the nuclear matrix proteins in a transgenic mouse model for prostate cancer [J].
Leman, ES ;
Arlotti, JA ;
Dhir, R ;
Greenberg, N ;
Getzenberg, RH .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2002, 86 (02) :203-212
[6]   Detection of prostate cancer using serum proteomics pattern in a histologically confirmed population [J].
Li, JN ;
White, N ;
Zhang, Z ;
Rosenzweig, J ;
Mangold, LA ;
Partin, AW ;
Chan, DW .
JOURNAL OF UROLOGY, 2004, 171 (05) :1782-1787
[7]   Confidence bounds when the estimated ROC area is 1.0 [J].
Obuchowski, NA ;
Lieber, ML .
ACADEMIC RADIOLOGY, 2002, 9 (05) :526-530
[8]  
PARTIN AW, 1993, CANCER RES, V53, P744
[9]   A COMMON SET OF NUCLEAR MATRIX PROTEINS IN PROSTATE-CANCER CELLS [J].
PIENTA, KJ ;
LEHR, JE .
PROSTATE, 1993, 23 (01) :61-67
[10]   Prevalence of prostate cancer among men with a prostate-specific antigen level ≤4.0 ng per milliliter [J].
Thompson, IM ;
Pauler, DK ;
Goodman, PJ ;
Tangen, CM ;
Lucia, MS ;
Parnes, HL ;
Minasian, LM ;
Ford, LG ;
Lippman, SM ;
Crawford, ED ;
Crowley, JJ ;
Coltman, CA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (22) :2239-2246