Reis Leonardo Oliveira, Zani Emerson Luis, García-Perdomo Herney Andrés
UroScience and Urology Department, Pontifical Catholic University of Campinas, Campinas, São Paulo, Brazil.
UROGIV Research Group, School of Medicine, Universidad del Valle, Cali, Colombia.
Int Urol Nephrol. 2018 Jun;50(6):993-1003. doi: 10.1007/s11255-018-1854-5. Epub 2018 Mar 29.
To evaluate the effectiveness and harms of DES in treating prostate cancer compared to other forms of androgen deprivation therapy (orchiectomy, LHRH agonists, and anti-androgens).
We included clinical trials comparing DES with other forms of ADT (bicalutamide, flutamide, LHRH agonists, or orchiectomy) in PCa treatment. The primary outcomes were overall survival, cancer-specific survival, and progression-free survival, and secondary outcomes were cardiovascular effects. We searched in MEDLINE, EMBASE, Central, and Lilacs from inception to nowadays and saturated information for unpublished data in other sources. We performed a qualitative analysis of all included studies. It was not possible to perform meta-analysis due to low-quality trials and high heterogeneity.
Overall, 1700 references were scanned and 14 prospective randomized trials with a total of 3986 patients were included in the final analysis. Although trials showed DES as similarly effective to another forms of ADT, evidences about cardiovascular toxicity in out of date high doses have discouraged its use. In doses of 1 mg, DES has been used as secondary line PCa treatment with safety.
DES might be similarly effective to other forms of ADT on advanced PCa patients, with potential important roles. Intriguingly, the burden of severe cardiovascular toxicity is mainly related to old-fashioned doses of 5.0 and 3.0 mg. Modern PCa hormonal knowledge warrants stout high-quality prospective randomized trials in the low-dose 1 mg DES scenario.
评估己烯雌酚(DES)与其他形式的雄激素剥夺疗法(睾丸切除术、促性腺激素释放激素(LHRH)激动剂和抗雄激素药物)相比,在治疗前列腺癌方面的有效性和危害。
我们纳入了比较DES与其他形式的雄激素剥夺疗法(比卡鲁胺、氟他胺、LHRH激动剂或睾丸切除术)用于前列腺癌治疗的临床试验。主要结局为总生存期、癌症特异性生存期和无进展生存期,次要结局为心血管效应。我们检索了从创刊至今的MEDLINE、EMBASE、CENTRAL和Lilacs数据库,并在其他来源中获取未发表数据的饱和信息。我们对所有纳入研究进行了定性分析。由于试验质量低和异质性高,无法进行荟萃分析。
总体而言,共筛选了1700篇参考文献,最终分析纳入了14项前瞻性随机试验,共3986例患者。尽管试验表明DES与其他形式的雄激素剥夺疗法效果相似,但关于过时高剂量DES心血管毒性的证据使其使用受到阻碍。在1毫克剂量下,DES已被安全地用作二线前列腺癌治疗。
DES对晚期前列腺癌患者可能与其他形式的雄激素剥夺疗法效果相似,具有潜在的重要作用。有趣的是,严重心血管毒性的负担主要与5.0毫克和3.0毫克的老式剂量有关。现代前列腺癌激素知识需要在低剂量1毫克DES情况下进行强有力的高质量前瞻性随机试验。