Benchmarking the efficacy of salvage systemic therapies for recurrent meningioma: A RANO group systematic review and meta-analysis to guide clinical trial design.

IF 13.4 1区 医学 Q1 CLINICAL NEUROLOGY
Rupesh Kotecha, Eyub Y Akdemir, Tugce Kutuk, Can Ilgın, Manmeet S Ahluwalia, Wenya L Bi, Jaishri Blakeley, Karan S Dixit, Ian F Dunn, Evanthia Galanis, Norbert Galldiks, Raymond Y Huang, Derek R Johnson, Thomas J Kaley, David O Kamson, Sylvia C Kurz, Michael W McDermott, Yazmin Odia, Matthias Preusser, Jeffrey Raizer, David A Reardon, C Leland Rogers, Roberta Ruda, David Schiff, Michael A Vogelbaum, Michael Weller, Patrick Y Wen, Minesh P Mehta
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引用次数: 0

Abstract

Background: Despite advances in our understanding of the molecular underpinnings of meningioma progression and innovations in systemic and local treatments, recurrent meningiomas remain a substantial therapeutic challenge. The objective of this systematic review and meta-analysis is to provide a historical baseline, contemporary analysis, and propose a "rate of probable interest" to inform future clinical trial design and development on behalf of the Response Assessment in Neuro-Oncology meningioma group.

Methods: PubMed, ClinicalTrials.gov, and ASCOpubs databases were screened for clinical trials evaluating the activity of systemic therapies for adults with recurrent meningiomas. The pooled progression-free survival at 6-months and 1-year (PFS-6 and PFS-1 year) values were calculated using the random effects technique with I2 indices.

Results: The pooled PFS-6 and PFS-1 year rates for recurrent WHO grade 1 meningiomas were 43.6% (95% CI: 22.7-67.0%, I2 = 80%) and 21.7% (95% CI: 6.2-53.9%, I2 = 76%), and for grades 2-3 meningiomas, the PFS-6 was 38.0% (95% CI: 28.3-48.8%, I2 = 68%). In the targeted therapy group, PFS-6 and PFS-1 year rates stood at 62.0% (I2 = 58%) and 49.0% (I2 = 63%) for grade 1, while for grades 2-3 tumors, the PFS-6 rates with targeted therapy and immunotherapy were 42.1% (I² = 60%) and 46.0% (I² = 0%), respectively. The benchmarks were set at 67% and 54% for PFS-6 and PFS-1 year for grade 1 tumors, and PFS-6 of 49% for grades 2-3 tumors.

Conclusions: Several studies have reported outcomes in patients with recurrent meningiomas testing a variety of agents with modest, but variable and progressively increasing activity. In this context, we recommend new benchmarks for future trials to define efficacy of future investigational therapies.

对复发性脑膜瘤的挽救性全身治疗的疗效进行基准评价:RANO组系统评价和指导临床试验设计的荟萃分析。
背景:尽管我们对脑膜瘤进展的分子基础的理解有所进展,并且在全身和局部治疗方面有所创新,但复发性脑膜瘤仍然是一个重大的治疗挑战。本系统综述和荟萃分析的目的是提供一个历史基线,当代分析,并提出一个“可能感兴趣的比率”,以代表RANO脑膜瘤组为未来的临床试验设计和开发提供信息。方法:PubMed、ClinicalTrials.gov和ASCOpubs数据库筛选评估成人复发性脑膜瘤全身疗法活性的临床试验。使用i平方指数随机效应技术计算6个月和1年(PFS-6和PFS-1年)的总无进展生存期。结果:WHO 1级脑膜瘤的PFS-6和PFS-1年复发率分别为43.6% (95% CI: 22.7-67.0%, I2=80%)和21.7% (95% CI: 6.2-53.9%, I2=76%), 2-3级脑膜瘤的PFS-6为38.0% (95% CI: 28.3-48.8%, I2=68%)。在靶向治疗组中,1级肿瘤的PFS-6和PFS-1年生存率分别为62.0% (I2=58%)和49.0% (I2=63%),而2-3级肿瘤,靶向治疗和免疫治疗的PFS-6年生存率分别为42.1% (I²=60%)和46.0% (I²=0%)。1级肿瘤PFS-6年和PFS-1年的基准分别为67%和54%,2-3级肿瘤PFS-6年的基准为49%。结论:几项研究报告了复发性脑膜瘤患者检测各种药物的结果,这些药物具有适度但可变且逐渐增加的活性。在这种情况下,我们建议为未来的试验制定新的基准,以确定未来研究性治疗的疗效。
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
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
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