Selumetinib for children with neurofibromatosis type 1 and plexiform neurofibromas: A plain language summary of SPRINT.

IF 3 4区 医学 Q2 ONCOLOGY
Future oncology Pub Date : 2024-05-01 Epub Date: 2024-02-22 DOI:10.2217/fon-2023-0565
Andrea M Gross, Colette Achée, Sarah E Hart, Lindsay Brewer, Andrea Baldwin, Pamela L Wolters, Brigitte C Widemann
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引用次数: 0

Abstract

What is this summary about?: This summary describes a publication about a study called SPRINT. The SPRINT study included 50 children with neurofibromatosis type 1 (NF1) and plexiform neurofibroma (PN) that could not be removed with surgery. PNs are tumors that grow along nerves and can cause various problems for children, such as pain, changes to appearance, and muscle weakness. In SPRINT, the study team wanted to learn whether a medication called selumetinib was able to shrink the PN caused by NF1 (also known as NF1-related PN), and if shrinking PNs helped relieve children of the problems caused by it. To assess how selumetinib might help, children had scans to measure the size of their PN, completed questionnaires, and had a variety of other tests done by their doctor. Their caregivers also completed questionnaires about their child. The children took selumetinib capsules twice a day on an empty stomach.

What were the results?: The results showed that selumetinib was able to shrink the PN for most children (68%). The results also showed that the problems caused by the children's PNs mostly improved while on selumetinib treatment. SPRINT also showed that the side effects of selumetinib were mainly mild and could be managed by doctors.

What do the results mean?: Before SPRINT, there were not many treatment options for children with NF1 and PN as there were no medications that had been shown to shrink PN, and surgery was not always possible. SPRINT showed that this medication shrinks most PNs and could help children with NF1 and PN. In April 2020, selumetinib was approved by the US Food and Drug Administration (FDA) because of the results of SPRINT. Selumetinib was the first and, as of February 2024, is the only medicine that can be prescribed by doctors to help children with NF1-related PN. Clinical Trial Registration: NCT01362803 (SPRINT) (ClinicalTrials.gov).

塞卢米替尼治疗1型神经纤维瘤病和丛状神经纤维瘤患儿:SPRINT 简明摘要。
本摘要是关于什么的? 本摘要介绍了一份关于名为 SPRINT 的研究的出版物。SPRINT研究包括50名患有神经纤维瘤病1型(NF1)和无法通过手术切除的丛状神经纤维瘤(PN)的儿童。神经纤维瘤是沿着神经生长的肿瘤,会给儿童带来各种问题,如疼痛、外观改变和肌肉无力。在 SPRINT 中,研究小组希望了解一种名为赛鲁米替尼的药物是否能够缩小由 NF1 引起的 PN(也称为 NF1 相关 PN),以及缩小 PN 是否有助于缓解儿童因 PN 引起的问题。为了评估色瑞替尼对治疗的帮助,孩子们接受了扫描以测量他们的PN大小,填写了调查问卷,并由他们的医生进行了各种其他测试。他们的看护人也填写了关于孩子的调查问卷。孩子们每天两次空腹服用赛鲁米替尼胶囊:结果表明,塞卢米替尼能够缩小大多数儿童(68%)的PN。结果还显示,在接受塞卢米替尼治疗期间,儿童PN引起的问题大多得到了改善。SPRINT还表明,塞卢米替尼的副作用主要是轻微的,医生可以控制。 SPRINT结果意味着什么? 在SPRINT之前,NF1和PN患儿的治疗选择并不多,因为没有任何药物被证明可以缩小PN,而且手术也不一定可行。SPRINT 表明,这种药物能缩小大多数 PN,可以帮助 NF1 和 PN 儿童。2020 年 4 月,由于 SPRINT 的结果,赛卢米替尼获得了美国食品和药物管理局(FDA)的批准。塞卢米替尼是第一种,也是截至2024年2月唯一一种可由医生处方用于帮助NF1相关PN患儿的药物。临床试验注册:NCT01362803(SPRINT)(ClinicalTrials.gov)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Future oncology
Future oncology ONCOLOGY-
CiteScore
5.40
自引率
3.00%
发文量
335
审稿时长
4-8 weeks
期刊介绍: Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community. The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.
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