Department of Clinical & Movement Neurosciences, UCL Institute of Neurology, London WC1N 3BG, UK.
Faculty of Health, University of Plymouth, Plymouth PL4 9AA, UK.
Brain. 2023 Jul 3;146(7):2717-2722. doi: 10.1093/brain/awad063.
An increase in the efficiency of clinical trial conduct has been successfully demonstrated in the oncology field, by the use of multi-arm, multi-stage trials allowing the evaluation of multiple therapeutic candidates simultaneously, and seamless recruitment to phase 3 for those candidates passing an interim signal of efficacy. Replicating this complex innovative trial design in diseases such as Parkinson's disease is appealing, but in addition to the challenges associated with any trial assessing a single potentially disease modifying intervention in Parkinson's disease, a multi-arm platform trial must also specifically consider the heterogeneous nature of the disease, alongside the desire to potentially test multiple treatments with different mechanisms of action. In a multi-arm trial, there is a need to appropriately stratify treatment arms to ensure each are comparable with a shared placebo/standard of care arm; however, in Parkinson's disease there may be a preference to enrich an arm with a subgroup of patients that may be most likely to respond to a specific treatment approach. The solution to this conundrum lies in having clearly defined criteria for inclusion in each treatment arm as well as an analysis plan that takes account of predefined subgroups of interest, alongside evaluating the impact of each treatment on the broader population of Parkinson's disease patients. Beyond this, there must be robust processes of treatment selection, and consensus derived measures to confirm target engagement and interim assessments of efficacy, as well as consideration of the infrastructure needed to support recruitment, and the long-term funding and sustainability of the platform. This has to incorporate the diverse priorities of clinicians, triallists, regulatory authorities and above all the views of people with Parkinson's disease.
在肿瘤学领域,通过使用多臂、多阶段试验,可以同时评估多种治疗候选药物,并为那些通过中期疗效信号的候选药物无缝招募到 3 期临床试验,成功地提高了临床试验的效率。在帕金森病等疾病中复制这种复杂的创新试验设计很有吸引力,但除了与评估帕金森病中单一潜在疾病修正干预措施的任何试验相关的挑战外,多臂平台试验还必须特别考虑到疾病的异质性,以及可能测试具有不同作用机制的多种治疗方法的愿望。在多臂试验中,需要适当地对治疗组进行分层,以确保每个组都与共享的安慰剂/标准治疗组进行比较;然而,在帕金森病中,可能更倾向于在一个臂中富集一组最有可能对特定治疗方法有反应的患者。解决这个难题的办法在于为每个治疗组制定明确的纳入标准,并制定一个分析计划,该计划考虑了预先定义的感兴趣亚组,同时评估每种治疗方法对更广泛的帕金森病患者群体的影响。除此之外,还必须有强有力的治疗选择流程和共识衍生的措施来确认靶点的参与以及中期疗效评估,以及考虑支持招募所需的基础设施,以及平台的长期资金和可持续性。这必须包含临床医生、试验者、监管机构的不同优先事项,最重要的是帕金森病患者的观点。