Hannah Louise Bromley, Mohini Varughese, Duncan C Gilbert, Peter J Hoskin, I. F. Tannock, Kimberley Reeves, Ananya Choudhury
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引用次数: 0
摘要
回顾低剂量与标准剂量恩杂鲁胺、阿帕鲁胺或达罗鲁胺治疗转移性前列腺癌的疗效和安全性。关键词检索:MEDLINE和EMBASE(截至2023年6月1日),并对可能相关的研究进行正向和反向引文检索。如果研究报告了接受减量恩杂鲁胺、阿帕鲁胺或达鲁胺治疗的转移性前列腺癌患者的主要结果数据,则纳入该研究。搜索仅限于原始全文和英文研究。主要结果包括总生存期(OS)、无进展生存期(PFS)、前列腺特异性抗原反应和治疗相关不良事件。该综述根据 Cochrane 快速综述方法小组指南进行。共确定了 10 项符合资格标准的研究:5 项 I 期研究、2 项 III 期试验的事后分析和 3 项回顾性分析。未发现OS、PFS与药物剂量之间存在一致的关联。本综述提供的证据表明,恩杂鲁胺、阿帕鲁胺或达罗鲁胺的用药剂量可低于标准推荐剂量,且不会丧失抗肿瘤活性。应进行前瞻性近等效随机试验,比较这些药物的注册剂量和较低剂量。
Comparison of standard-dose and reduced-dose treatment of metastatic prostate cancer with enzalutamide, apalutamide or darolutamide: a rapid review
To review the efficacy and safety of low-dose versus standard-dose enzalutamide, apalutamide or darolutamide treatment for metastatic prostate cancer.Keyword searches in MEDLINE and EMBASE up to 1 June 2023, with forward and backward citation searches of potentially relevant studies. Studies were included if primary outcome data were reported for patients with metastatic prostate cancer who had received reduced doses of enzalutamide, apalutamide or darolutamide. Searches were limited to original full-text and English-language studies. Key outcomes included overall survival (OS), progression-free survival (PFS), prostate-specific antigen response and treatment-related adverse events. The review was performed in accordance with Cochrane Rapid Reviews Methods Group guidelines.Ten studies were identified that met the eligibility criteria: five phase I studies, two post-hoc analyses of phase III trials and three retrospective analyses. No consistent association between OS, PFS and drug dose was identified. Fewer severe treatment-related adverse events were observed at lower drug doses.This review provides evidence that enzalutamide, apalutamide or darolutamide could be given at a lower than the standard recommended dose without loss of antitumour activity. A prospective near-equivalence randomised trial should be undertaken to compare registered and lower doses of these agents.CRD42023440371.