Mueller-Lisse Ullrich G, Mueller-Lisse Ulrike L, Haller Steffen, Schneede Peter, Scheidler Juergen E, Schmeller Nicolaus, Hofstetter Alfons G, Reiser Maximilian F
Department of Radiology, Klinikum Grosshadern, University of Munich, Germany.
J Comput Assist Tomogr. 2002 May-Jun;26(3):432-7. doi: 10.1097/00004728-200205000-00020.
As a screening test for prostate cancer (PCA), prostate-specific antigen (PSA) may induce unnecessary prostate biopsy in patients with PSA 4.1-10.0 ng/ml. PCA detection may be delayed in patients with PSA < or =4.0 ng/ml. MRI-based PSA density of the prostate (PSAD) and of the prostatic transitional zone (PSAT) could improve differentiation of PCA and benign prostatic hyperplasia.
Total prostate and transitional zone volumes were planimetrically determined in axial, T2-weighted fast spin echo MR images of the prostate. Serum PSA concentration was measured with an automated standardized microparticle enzyme immune assay. PSAD and PSAT were calculated in 17 patients with clinically significant PCA and 42 patients with benign prostatic hypertrophy (BPH) (66 +/- 6 versus 64 +/- 8 years, p = 0.2410, t test) who had PSA levels < or =10.0 ng/ml.
For differentiation of BPH and PCA, PSA alone above the optimal cutoff level of 4.2 ng/ml showed an odds ratio for PCA of 6.7 (95% confidence interval [CI], 1.9-23.2). PSAD showed an odds ratio for PCA of 71.3 (95% CI, 11.8-430.9) above the optimal cutoff level of 0.07 ng/ml/cc. PSAT demonstrated an odds ratio for PCA of 320.0 (95% CI, 27.1-3781.4) above the optimal cutoff level of 0.15 ng/ml/cc.
In patients with PSA < or =10.0 ng/ml, MRI-based PSAD and PSAT appear to improve differentiation of prostate cancer and BPH and are feasible to reduce the frequency of unnecessary prostate biopsy.
作为前列腺癌(PCA)的筛查试验,前列腺特异性抗原(PSA)可能会导致PSA水平在4.1 - 10.0 ng/ml的患者进行不必要的前列腺活检。PSA水平≤4.0 ng/ml的患者中PCA检测可能会延迟。基于磁共振成像(MRI)的前列腺PSA密度(PSAD)和前列腺移行区PSA密度(PSAT)可改善PCA与良性前列腺增生的鉴别。
在前列腺的轴位T2加权快速自旋回波MR图像上通过平面测量法确定前列腺总体积和移行区体积。采用自动化标准化微粒酶免疫测定法测量血清PSA浓度。计算了17例具有临床意义的PCA患者和42例良性前列腺增生(BPH)患者(年龄分别为66±6岁和64±8岁,p = 0.2410,t检验)的PSAD和PSAT,这些患者的PSA水平≤10.0 ng/ml。
对于BPH和PCA的鉴别,单独PSA高于最佳临界值4.2 ng/ml时,PCA的优势比为6.7(95%置信区间[CI],1.9 - 23.2)。PSAD高于最佳临界值0.07 ng/ml/cc时,PCA的优势比为71.3(95% CI,11.8 - 430.9)。PSAT高于最佳临界值0.15 ng/ml/cc时,PCA的优势比为320.0(95% CI,27.1 - 3781.4)。
在PSA水平≤10.0 ng/ml的患者中,基于MRI的PSAD和PSAT似乎可改善前列腺癌与BPH的鉴别,并且在减少不必要的前列腺活检频率方面是可行的。