Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri; Koç University School of Medicine, Istanbul, Turkey.
University of Washington School of Medicine, Seattle, Washington.
Pediatr Neurol. 2022 Sep;134:1-6. doi: 10.1016/j.pediatrneurol.2022.06.003. Epub 2022 Jun 10.
The neurofibromatoses comprise three different genetic conditions causing considerable morbidity and mortality: neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and schwannomatosis (SWN). This review summarizes recent and ongoing clinical trials involving patients with neurofibromatoses to better understand the current state of clinical trial research centered around these conditions and inform areas of need.
A search was conducted using the Cochrane Central Register of Controlled Trials and clinicaltrials.gov databases. Inclusion and exclusion criteria were designed to identify clinical trials focused on patients with NF1, NF2, or SWN completed in or after 2010 and in process as of December 31, 2021. Information was collected using standardized guidelines.
A total of 134 clinical trials were included, with 75 (56%) completed and 59 (44%) in process. For completed trials, 74% (n = 56) involved patients with NF1, and of those based on specific tumors (n = 26, 46%), the majority focused on plexiform neurofibromas (PNs) (n = 12, 46%). For ongoing trials, 79% (n = 47) involve patients with NF1, and of those based on specific tumors (n = 29, 61%), the majority are focused on PNs (n = 13, 45%).
Both recent and ongoing clinical trials have primarily focused on patients with NF1 and the treatment of PNs. This research has led to the first FDA-approved drug for NF1-PN and has changed management of these tumors, allowing for systemic therapy rather than reliance on only a surgical modality. Trials evaluating comorbid psychiatric conditions and quality of life among patients with any of the neurofibromatoses appear less common. These areas may warrant focus in future studies to improve clinical management.
神经纤维瘤病包括三种不同的遗传疾病,会导致相当大的发病率和死亡率: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)。本综述总结了最近和正在进行的涉及神经纤维瘤病患者的临床试验,以更好地了解围绕这些疾病的临床试验研究现状,并确定需要关注的领域。
使用 Cochrane 中央对照试验注册库和 clinicaltrials.gov 数据库进行了搜索。纳入和排除标准旨在确定 2010 年及以后完成或正在进行的、针对 NF1、NF2 或 SWN 患者的临床试验,并于 2021 年 12 月 31 日截止。使用标准化指南收集信息。
共纳入 134 项临床试验,其中 75 项(56%)已完成,59 项(44%)正在进行中。对于已完成的试验,74%(n=56)涉及 NF1 患者,其中基于特定肿瘤的试验(n=26,46%),大多数集中在丛状神经纤维瘤(PNs)(n=12,46%)。对于正在进行的试验,79%(n=47)涉及 NF1 患者,其中基于特定肿瘤的试验(n=29,61%),大多数集中在 PNs(n=13,45%)。
最近和正在进行的临床试验主要集中在 NF1 患者和 PNs 的治疗上。这项研究导致了第一个 FDA 批准用于 NF1-PN 的药物,并改变了这些肿瘤的治疗方法,允许进行系统治疗,而不仅仅依赖于手术方式。评估任何一种神经纤维瘤病患者伴发的共病性精神疾病和生活质量的试验似乎较少。这些领域可能需要在未来的研究中重点关注,以改善临床管理。