Smith J A, Lange P H, Janknegt R A, Abbou C C, deGery A
Department of Urologic Surgery, Vanderbilt University, Nashville, Tennessee, USA.
J Urol. 1997 Apr;157(4):1329-34.
Prostate specific antigen (PSA), prostatic acid phosphatase and alkaline phosphatase were analyzed in 2 large prospective multicenter and multinational trials to assess their correlation with time to progression and overall survival after hormonal therapy for metastatic carcinoma of the prostate.
A total of 868 patients who underwent medical or surgical castration was randomized to receive an oral antiandrogen (nilutamide) or placebo. The serum markers under study were measured at baseline and at 1, 3, 6 and every 6 months thereafter.
At baseline the strongest predictive factor was serum alkaline phosphatase. Patients with an alkaline phosphatase of 2 or less times normal lived almost twice as long as those with a level of more than 2 times normal (p < 0.0001). The longer survival was observed in patients whose PSA became normal 3 months after initiation of hormonal therapy compared to those whose PSA never reached normal (p < 0.0001).
Serum markers at baseline and during the few months after initiation of hormonal therapy can provide prognostic information for the clinical treatment of patients with metastatic carcinoma of the prostate. In addition, the PSA level at month 3 can serve as a surrogate end point in clinical trials.
在两项大型前瞻性多中心和跨国试验中,对前列腺特异性抗原(PSA)、前列腺酸性磷酸酶和碱性磷酸酶进行分析,以评估它们与前列腺癌激素治疗后疾病进展时间和总生存期的相关性。
共有868例接受药物或手术去势的患者被随机分为两组,分别接受口服抗雄激素药物(尼鲁米特)或安慰剂治疗。在基线时以及之后的第1、3、6个月和此后每6个月测量所研究的血清标志物。
在基线时,最强的预测因素是血清碱性磷酸酶。碱性磷酸酶水平为正常上限2倍及以下的患者的生存期几乎是该水平高于正常上限2倍患者的两倍(p < 0.0001)。与PSA从未恢复正常的患者相比,激素治疗开始3个月后PSA恢复正常的患者生存期更长(p < 0.0001)。
基线时以及激素治疗开始后的几个月内的血清标志物可为前列腺癌转移患者的临床治疗提供预后信息。此外,第3个月时的PSA水平可作为临床试验中的替代终点。