Sridhara R, Eisenberger M A, Sinibaldi V J, Reyno L M, Egorin M J
Department of Epidemiology and Preventive Medicine, Marlene and Stewart Greenbaum Cancer Center at the University of Maryland, Baltimore 21201, USA.
Cancer Epidemiol Biomarkers Prev. 1998 Jul;7(7):631-4.
Hormone-refractory prostate cancer (HRPC) patients often have nonmeasurable disease. In such patients, predictive biomarkers other than tumor response may be required to compare therapeutic effects. We examined the predictive value for survival of various clinical and laboratory parameters, including prostate-specific antigen (PSA), in HRPC patients treated with suramin. Data from 103 HRPC patients were analyzed using various survival analyses, the likelihood ratio approach, and logistic regression analyses. When pretreatment factors, percentage decrease in PSA at 4 weeks from start of treatment (deltaPSA), and updated survival data were fit by a multivariate Cox proportional hazards model, acid phosphatase, lactate dehydrogenase, and deltaPSA were significant, with risk ratios close to 1. There was a decrease in likelihood ratio with increasing APSA. A logistic regression model was developed to predict the probability of <1 year of survival from the start of treatment. Hemoglobin and deltaPSA were found to be significant variables. However, in view of the complexities involving the relationship between PSA expression and prostate cancer growth and possible selective effect of treatment on PSA, further prospective testing is necessary. Therefore, deltaPSA cannot necessarily be used as a biomarker for survival response in individual patients during the evaluation of the therapeutic response of HRPC to new antineoplastic drugs.
激素难治性前列腺癌(HRPC)患者常出现不可测量的疾病。在此类患者中,可能需要肿瘤反应以外的预测性生物标志物来比较治疗效果。我们研究了在接受苏拉明治疗的HRPC患者中,包括前列腺特异性抗原(PSA)在内的各种临床和实验室参数对生存的预测价值。使用各种生存分析、似然比方法和逻辑回归分析对103例HRPC患者的数据进行了分析。当通过多变量Cox比例风险模型拟合预处理因素、治疗开始后4周时PSA的下降百分比(deltaPSA)以及更新后的生存数据时,酸性磷酸酶、乳酸脱氢酶和deltaPSA具有显著性,风险比接近1。随着APSA的增加,似然比降低。建立了一个逻辑回归模型来预测从治疗开始起生存<1年的概率。发现血红蛋白和deltaPSA是显著变量。然而,鉴于PSA表达与前列腺癌生长之间关系的复杂性以及治疗对PSA可能的选择性作用,有必要进行进一步的前瞻性试验。因此,在评估HRPC对新型抗肿瘤药物的治疗反应时,deltaPSA不一定能用作个体患者生存反应的生物标志物。