Shelley M D, Kumar S, Coles B, Wilt T, Staffurth J, Mason M D
Cochrane Urological Cancers Unit, Research Department, Velindre NHS Trust, Cardiff CF14 2TL, UK.
Cancer Treat Rev. 2009 Nov;35(7):540-6. doi: 10.1016/j.ctrv.2009.05.001. Epub 2009 Jun 2.
Adjuvant hormone therapy (AHT) following radiotherapy or surgery is a treatment option frequently offered to men with localised or locally advanced prostate cancer. We performed a systematic review of published randomised trials to assess the effectiveness of AHT.
We searched MEDLINE, EMBASE, the Cochrane library, SCI, LILACS and SIGLE for randomised trials comparing AHT plus primary therapy (radiotherapy or prostatectomy) with primary therapy alone. Data on study design, participants interventions and outcomes were extracted from relevant studies and where possible pooled for meta-analysis.
AHT following radiotherapy improved overall survival (at 5 years OR fixed effect model 1.29, 95% CI 1.07-1.56, p=0.007), disease-specific survival (OR 2.10, 95% CI 1.53-2.88, p<0.00001) and disease-free survival (OR 1.91, 95% CI 1.16-2.23, p<0.00001). A random effect model favoured adjuvant hormone therapy but did not reach significance. After prostatectomy, there was no significant overall survival advantage with AHT, although one study reported a significant improvement in disease-specific survival (HR 4.09, p=0.0004). Disease-free survival was also better with AHT (OR 3.73, 95% CI 2.30-6.03, p<0.00001). AHT-induced toxicities included gynaecomastia, impotence, gastrointestinal and haematological.
There are significant clinical benefits associated with the use of AHT for early prostate cancer. Patients should make an informed decision to accept AHT based on its effectiveness and side-effects.
放疗或手术后的辅助激素治疗(AHT)是经常为局限性或局部晚期前列腺癌男性患者提供的一种治疗选择。我们对已发表的随机试验进行了系统评价,以评估AHT的有效性。
我们检索了MEDLINE、EMBASE、Cochrane图书馆、SCI、LILACS和SIGLE,查找比较AHT加主要治疗(放疗或前列腺切除术)与单纯主要治疗的随机试验。从相关研究中提取关于研究设计、参与者干预措施和结果的数据,并在可能的情况下进行汇总以进行荟萃分析。
放疗后的AHT改善了总生存期(5年时,固定效应模型的比值比为1.29,95%可信区间为1.07 - 1.56,p = 0.007)、疾病特异性生存期(比值比为2.10,95%可信区间为1.53 - 2.88,p < 0.00001)和无病生存期(比值比为1.91,95%可信区间为1.16 - 2.23,p < 0.00001)。随机效应模型支持辅助激素治疗,但未达到显著水平。前列腺切除术后,AHT在总生存期方面没有显著优势,尽管一项研究报告疾病特异性生存期有显著改善(风险比为4.09,p = 0.0004)。AHT组的无病生存期也更好(比值比为3.73,95%可信区间为2.30 - 6.03,p < 0.00001)。AHT引起的毒性包括男性乳房发育、阳痿、胃肠道和血液系统问题。
早期前列腺癌使用AHT有显著的临床益处。患者应根据其有效性和副作用做出明智的决定,以接受AHT。