单中心病例研究系列,评估神经纤维瘤病相关丛状神经纤维瘤患者使用赛鲁米尼的效果。

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2024-10-22 eCollection Date: 2024-01-01 DOI:10.1093/noajnl/vdae177
João Passos, Marta P Soares, Duarte Salgado, Sofia Nunes, Daniela Cavaco, Pedro M Garrido, Mónica Coutinho, Inês Patrocínio Carvalho, Miguel Vilares, Mafalda Ferreira, Cristina Lacerda
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引用次数: 0

摘要

背景:神经纤维瘤病1型(NF1)是一种常见的遗传性疾病,表型多变,具有年龄依赖性渗透。本研究描述了在真实世界临床环境中使用赛鲁米替尼治疗丛状神经纤维瘤(PN)的大型患者队列的诊断、临床特征、管理和疗效:这项单中心观察性研究连续招募了2018年4月至2023年期间接受赛鲁米替尼治疗的NF1-PN患者。基线时记录了临床特征、肿瘤类型和位置以及基因检测结果等数据;记录了使用赛鲁米替尼和手术干预进行疾病管理的详情以及疾病演变情况,包括影像学数据以及疼痛和功能评估:共纳入54名患者,中位年龄(范围)为16.4(4.5-58.0)岁。大多数患者有皮肤表现(88.9%),包括皮肤神经纤维瘤和PN。患者在治疗前接受了[18F]氟脱氧葡萄糖(FDG)-PET/CT成像,以排除恶性病变。初步评估包括定向磁共振成像(MRI),这有助于今后的比较,并可评估 PN 的可切除性。使用色瑞替尼进行药物治疗(配合手术,不配合手术)后,获得疾病稳定(58.8%,54.3%)、部分应答(29.4%,28.6%)以及疼痛改善(58.8%,37.1%)、畸形改善(17.6%,20.0%)和功能改善(17.6%,20.0%)的患者比例分别如下:这项研究的结果表明,NF1-PN可通过手术干预与赛鲁米替尼进行有效治疗。大多数患者的肿瘤得到了稳定,症状控制也得到了改善,而且大多数患者仍在继续接受治疗。通过FDG-PET/CT和MRI成像的个体化应用以及有针对性的资源分配,实现了有效的诊断和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A single-center case study series assessing the effect of selumetinib use in patients with neurofibromatosis-related plexiform neurofibromas.

Background: Neurofibromatosis type 1 (NF1) is a common genetic disorder of phenotypic variability with age-dependent penetrance. This study describes the diagnosis, clinical characterization, management, and outcomes of a large patient cohort with plexiform neurofibroma (PN) treated with selumetinib in a real-world clinical setting.

Methods: This single-center observational study consecutively enrolled patients with NF1-PN treated with selumetinib from April 2018 to 2023. Data on clinical features, tumor types and locations, and results from genetic tests were recorded at baseline; details of disease management with selumetinib and surgical intervention and disease evolution including imaging data and evaluations of pain and function were documented.

Results: Overall, 54 patients with a median age (range) of 16.4 (4.5-58.0) years were enrolled. Most had cutaneous manifestations (88.9%), including cutaneous neurofibromas and PN. Patients underwent [18F]fluorodeoxyglucose (FDG)-PET/CT imaging before treatment to rule out malignant lesions. Initial evaluations included directed magnetic resonance imaging (MRI), which facilitated future comparisons and allowed for the assessment of PN resectability. Pharmacological treatment with selumetinib (with surgery, without surgery) resulted in the following proportion of patients achieving stable disease (58.8%, 54.3%), partial response (29.4%, 28.6%), and improved pain (58.8%, 37.1%), deformity (17.6%, 20.0%), and functional (17.6%, 20.0%) outcomes, respectively.

Conclusions: Results from this study demonstrate that NF1-PN can be managed effectively with selumetinib with surgical intervention in some patients. Most patients achieved tumor stability and improved symptom control, and the majority of patients continue under treatment. Effective diagnosis and management were achieved through individualized utility of FDG-PET/CT and MRI imaging and targeted resource allocation.

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