Department of Urology, Hasan Sadikin Academic Medical Center, Universitas Padjajaran Bandung, Indonesia.
Asian Pac J Cancer Prev. 2021 Oct 1;22(10):3101-3107. doi: 10.31557/APJCP.2021.22.10.3101.
This systematic review aimed to determine the efficacy of ketoconazole in the treatment of metastatic castration-resistant prostate cancer (mCRPC).
A literature search was performed on four databases of PubMed, Google Scholar, Cochrane Database of Systematic Reviews, and Directory of Open Access Journals (DOAJ). The initial search resulted in 602 articles, which were progressively eliminated based on duplication, irrelevancy, and unsuitable methodology. A total of seventeen articles were included in the final analysis, including four randomized controlled trials, nine retrospective cohorts, and four prospective cohorts, with a total population of 1,095 patients. A 200-400 mg, tid dose of ketoconazole was used in these studies along with corticoid replacement therapy with hydrocortisone, 20-30 mg in the morning and 10-20 mg in the evening, or prednisone, 5 mg, bid.
Based on our findings, 8 out of 17 studies reported PSA decrease of >50% in approximately half of the population, with a more significant PSA response at 400 mg ketoconazole dosage, and the average progression-free survival (PFS) of 2.6-14.5 months, or time to progression of 3.2-6.7 months.
Ketoconazole with corticosteroid could be an effective alternative for the treatment of mCRPC with a satisfactory PSA response and disease progression.
本系统评价旨在确定酮康唑治疗转移性去势抵抗性前列腺癌(mCRPC)的疗效。
在 PubMed、Google Scholar、Cochrane 系统评价数据库和开放获取期刊目录(DOAJ)这四个数据库中进行了文献检索。最初的搜索结果为 602 篇文章,根据重复、不相关和不适当的方法逐步淘汰。最终分析共纳入 17 篇文章,包括 4 项随机对照试验、9 项回顾性队列研究和 4 项前瞻性队列研究,总共有 1095 例患者。这些研究中使用的酮康唑剂量为 200-400mg,tid,同时合用皮质类固醇替代疗法,即氢化可的松,早晨 20-30mg,晚上 10-20mg,或泼尼松,5mg,bid。
根据我们的研究结果,17 项研究中有 8 项报告了约一半人群 PSA 下降>50%,酮康唑剂量为 400mg 时 PSA 反应更显著,平均无进展生存期(PFS)为 2.6-14.5 个月,或进展时间为 3.2-6.7 个月。
酮康唑联合皮质类固醇可能是治疗 mCRPC 的有效替代方案,具有令人满意的 PSA 反应和疾病进展。