Department of General Paediatrics, Sophia's Children's Hospital, Rotterdam, the Netherlands; ENCORE, Erasmus MC Rotterdam, the Netherlands.
Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust London, UK.
Eur J Med Genet. 2021 Sep;64(9):104281. doi: 10.1016/j.ejmg.2021.104281. Epub 2021 Jul 5.
Neurofibromatosis (NF) is the umbrella term for neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) and schwannomatosis (SWN). EU-PEARL aims to create a framework for platform trials in NF. The aim of this systematic review is to create an overview of recent clinical drug trials in NF, to identify learning points to guide development of the framework. We searched Embase, Medline and Cochrane register of trials on October 1, 2020 for publications of clinical drug trials in NF patients. We excluded publications published before 2010, systematic reviews, secondary analyses and studies with <10 patients. Data was extracted on manifestations studied, study design, phase, number of participating centres and population size. Full-text review resulted in 42 articles: 31 for NF1, 11 for NF2, none for SWN. Most NF1 trials focused on plexiform neurofibromas (32%). Trials in NF2 solely studied vestibular schwannomas. In NF1, single-arm trials (58%) were most common, and the majority was phase II (74%). For NF2 most trials were single-arm (55%) and exclusively phase II. For both diseases, trials were predominantly single-country and included five centres or less. Study population sizes were small, with the majority including ≤50 patients (74%). In conclusion, NF research is dominated by studies on a limited number out of the wide range of manifestations. We need more trials for cutaneous manifestations and high-grade gliomas in NF1, manifestations other than vestibular schwannoma in NF2 and trials for SWN. Drug development in NF may profit from innovative trials on multiple interventions and increased international collaboration.
神经纤维瘤病(NF)是神经纤维瘤病 1 型(NF1)、神经纤维瘤病 2 型(NF2)和许旺细胞瘤病(SWN)的统称。EU-PEARL 旨在为 NF 平台试验创建一个框架。本系统评价的目的是对 NF 近期临床药物试验进行概述,以确定指导框架制定的学习要点。我们于 2020 年 10 月 1 日在 Embase、Medline 和 Cochrane 试验注册库中搜索了 NF 患者临床药物试验的出版物。我们排除了 2010 年前发表的出版物、系统评价、二次分析和纳入患者数<10 人的研究。提取了研究中研究的表现、研究设计、阶段、参与中心数量和人口规模的数据。全文审查结果为 42 篇文章:31 篇用于 NF1,11 篇用于 NF2,无 SWN。大多数 NF1 试验集中在丛状神经纤维瘤(32%)上。NF2 的试验仅研究前庭神经鞘瘤。在 NF1 中,单臂试验(58%)最常见,多数为 II 期(74%)。对于 NF2,大多数试验为单臂(55%)且仅为 II 期。两种疾病的试验主要为单中心,纳入 5 个中心或更少。研究人群规模较小,多数纳入患者数≤50 例(74%)。总之,NF 研究主要集中在少数临床表现上,而临床表现范围广泛。我们需要更多针对 NF1 的皮肤表现和高级别胶质瘤、NF2 中除前庭神经鞘瘤以外的表现以及 SWN 的试验。NF 的药物开发可能受益于针对多种干预措施的创新试验和增加的国际合作。