Sciarra Alessandro, Voria Giuseppe, Monti Salvatore, Mazzone Luigi, Mariotti Gianna, Pozza Mariangela, D'Eramo Giuseppe, Silverio Franco Di
University La Sapienza, Department of Urology, Rome, Italy.
Prostate. 2004 Mar 1;58(4):421-8. doi: 10.1002/pros.10347.
To evaluate whether the pretreatment determination of serum chromogranin A (CgA) can provide information beyond that obtained with serum prostate specific antigen (PSA) and Gleason score at biopsy as a predictive factor of clinical understaging (T2-pT3) of prostate adenocarcinoma.
In this prospective study, we analyzed 83 consecutive patients with clinical T2N0M0 prostate adenocarcinoma submitted to radical prostatectomy (RRP). On the same day of RRP, before surgery, a blood sample for the determination of serum total PSA and CgA levels (RIA) was obtained.
After RRP, 27 of the 83 cases (32.5%) showed extracapsular disease extension (pT3) at the final pathological examination and were considered clinically understaged. A significant association between serum CgA and pathological stage (r = 0.3830; P = 0.0004) was found. At the multivariate analysis, serum CgA and PSA, but not biopsy Gleason score, were found to be significant pretreatment independent predictors of pT3 at RRP (P = 0.00004 and P = 0.0018, respectively). The relative risk of clinical understaging significantly varied according to serum CgA levels. Using a CgA cut-off value of 60 ng/ml, PPV and NPV for clinical understaging were 0.5161 and 0.7885, respectively (P = 0.0072).
Serum CgA could be incorporated into risk assessment models of newly diagnosed prostate cancer.
评估术前测定血清嗜铬粒蛋白A(CgA)是否能提供超越血清前列腺特异性抗原(PSA)和活检时Gleason评分所获得的信息,作为前列腺腺癌临床分期过低(T2-pT3)的预测因素。
在这项前瞻性研究中,我们分析了83例连续接受根治性前列腺切除术(RRP)的临床T2N0M0前列腺腺癌患者。在RRP当天手术前,采集血样用于测定血清总PSA和CgA水平(放射免疫分析)。
RRP后,83例中的27例(32.5%)在最终病理检查时显示有包膜外疾病扩展(pT3),被认为临床分期过低。发现血清CgA与病理分期之间存在显著相关性(r = 0.3830;P = 0.0004)。在多变量分析中,发现血清CgA和PSA是RRP时pT3的术前独立显著预测因素,而活检Gleason评分不是(P分别为0.00004和0.0018)。临床分期过低的相对风险根据血清CgA水平有显著差异。使用CgA临界值60 ng/ml时,临床分期过低的阳性预测值(PPV)和阴性预测值(NPV)分别为0.5161和0.7885(P = 0.0072)。
血清CgA可纳入新诊断前列腺癌的风险评估模型。