Seidenfeld J, Samson D J, Hasselblad V, Aronson N, Albertsen P C, Bennett C L, Wilt T J
Blue Cross and Blue Shield Association Technology Evaluation Center, Chicago, Illinois 60601-7680, USA.
Ann Intern Med. 2000 Apr 4;132(7):566-77. doi: 10.7326/0003-4819-132-7-200004040-00009.
To compare luteinizing hormone-releasing hormone (LHRH) agonists with orchiectomy or diethylstilbestrol, and to compare antiandrogens with any of these three alternatives.
A search of the MEDLINE, Cancerlit, EMBASE, and Cochrane Library databases from 1966 to March 1998 and Current Contents to 24 August 1998 for articles comparing the outcomes of the specified treatments. The search was limited to studies on prostatic neoplasms in humans. Total yield was 1477 studies.
Reports of efficacy outcomes were limited to randomized, controlled trials. Twenty-four trials involving more than 6600 patients, phase II studies that reported on withdrawals from therapy (the most reliable indicator of adverse effects), and all studies reporting on quality of life were abstracted.
Two independent reviewers abstracted each article by following a prospectively designed protocol. The meta-analysis combined data on 2-year overall survival by using a random-effects model and; reported results as a hazard ratio relative to orchiectomy.
Ten trials of LHRH agonists involving 1908 patients reported no significant difference in overall survival. The hazard ratio showed LHRH agonists to be essentially equivalent to orchiectomy (hazard ratio, 1.1262 [corrected] [95% CI, 0.915 to 1.386]). There was no evidence of difference in overall survival among the LHRH agonists, although CIs were wider for leuprolide (hazard ratio, 1.0994 [CI, 0.207 to 5.835]) and buserelin (hazard ratio, 1.1315 [CI, 0.533 to 2.404]) than for goserelin (hazard ratio, 1.1172 [CI, 0.898 to 1.390]). Evidence from 8 trials involving 2717 patients suggests that nonsteroidal antiandrogens were associated with lower overall survival. The CI for the hazard ratio approached statistical significance (hazard ratio, 1.2158 [CI, 0.988 to 1.496]). Treatment withdrawals were less frequent with LHRH agonists (0% to 4%) than with nonsteroidal antiandrogens (4% to 10%).
Survival after therapy with an LHRH agonist was equivalent to that after orchiectomy. No evidence shows a difference in effectiveness among the LHRH agonists. Survival rates may be somewhat lower if a nonsteroidal antiandrogen is used as monotherapy.
比较促黄体生成激素释放激素(LHRH)激动剂与睾丸切除术或己烯雌酚,并比较抗雄激素药物与这三种治疗方法中的任何一种。
检索1966年至1998年3月的MEDLINE、Cancerlit、EMBASE和Cochrane图书馆数据库以及截至1998年8月24日的《现刊目次》,以查找比较指定治疗方法疗效的文章。检索仅限于关于人类前列腺肿瘤的研究。共检索到1477项研究。
疗效结果报告仅限于随机对照试验。提取了24项涉及6600多名患者的试验、报告治疗退出情况(不良反应最可靠指标)的II期研究以及所有报告生活质量的研究。
两名独立审阅者按照预先设计的方案提取每篇文章的数据。荟萃分析采用随机效应模型合并2年总生存数据,并将结果报告为相对于睾丸切除术的风险比。
10项涉及1908例患者的LHRH激动剂试验报告总生存无显著差异。风险比显示LHRH激动剂与睾丸切除术基本等效(风险比,1.1262[校正][95%CI,0.915至1.386])。虽然亮丙瑞林(风险比,1.0994[CI,0.207至5.835])和布舍瑞林(风险比,1.1315[CI,0.533至2.404])的CI比戈舍瑞林(风险比,1.1172[CI,0.898至1.390])宽,但没有证据表明LHRH激动剂之间总生存存在差异。8项涉及2717例患者的试验证据表明,非甾体类抗雄激素药物与较低的总生存率相关。风险比的CI接近统计学显著性(风险比,1.2158[CI,0.988至1.496])。LHRH激动剂的治疗退出率(0%至4%)低于非甾体类抗雄激素药物(4%至10%)。
LHRH激动剂治疗后的生存率与睾丸切除术后相当。没有证据表明LHRH激动剂之间疗效存在差异。如果将非甾体类抗雄激素药物作为单一疗法,生存率可能会略低。