Low-Grade Glioma Clinical Trials in the United States: A Systematic Review.

IF 3.2 3区 生物学 Q1 BIOLOGY
Life-Basel Pub Date : 2024-09-09 DOI:10.3390/life14091133
Emily Xu, Jonathan Patterson, Angelo Angione, Alexander Li, David W Wu, Ebrar Akca, Omar Elghawy, Alexander Barsouk, Jonathan H Sussman
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引用次数: 0

Abstract

Low-grade glioma (LGG) is a malignancy of the central nervous system that is often treatable with surgical resection and chemoradiation. However, despite an initial positive response to standard therapy, most LGG eventually progress to high-grade gliomas which are nearly uniformly fatal. There is a pressing need for more clinical trials and greater clinical trial accessibility to improve the standard of care of LGG to delay or prevent its progression. In this study, we systematically examined the scope and inclusion of clinical trials for LGG based in the United States. This cross-sectional study analyzes trends in trial design and reported demographic data from completed LGG trials registered on ClinicalTrials.gov between 2010 to 2023. Inclusion criteria, investigational therapies, primary outcomes, and preliminary results were compared and summarized. A total of 14 trials with 1067 participants were included in the study. Most of the trials were not exclusive to LGGs and 14% had mutation-specific inclusion criteria. To date, two of the trials have led to new FDA-approved treatments. All trials reported age and sex, while only 57% reported race and 43% reported ethnicity. Individuals identifying as Black or African American and Asian or Pacific Islander were statistically underrepresented. Lastly, we investigated the geographic distributions of trial sites across the United States, which demonstrated several coverage gaps in the Rocky Mountain and Southeast regions. These findings suggest specific areas for improvement in LGG clinical trial reporting and accessibility.

美国的低级别胶质瘤临床试验:系统回顾。
低级别胶质瘤(LGG)是一种中枢神经系统恶性肿瘤,通常可以通过手术切除和化学放疗来治疗。然而,尽管最初对标准疗法有积极反应,但大多数低级别胶质瘤最终会发展为高级别胶质瘤,而高级别胶质瘤几乎都是致命的。目前迫切需要更多的临床试验和更大的临床试验可及性,以改善LGG的标准治疗,延缓或防止其进展。在这项研究中,我们系统地考察了美国针对 LGG 的临床试验的范围和纳入情况。这项横断面研究分析了 2010 年至 2023 年期间在 ClinicalTrials.gov 上注册的已完成 LGG 试验的试验设计趋势和报告的人口统计学数据。对纳入标准、研究疗法、主要结果和初步结果进行了比较和总结。研究共纳入了14项试验,1067名参与者。大多数试验并非只针对LGGs,14%的试验有特定突变的纳入标准。迄今为止,其中两项试验已开发出获得美国食品药品管理局批准的新疗法。所有试验都报告了年龄和性别,但只有 57% 的试验报告了种族,43% 的试验报告了民族。据统计,黑人或非裔美国人以及亚裔或太平洋岛民所占比例较低。最后,我们调查了全美试验点的地理分布情况,结果显示落基山和东南部地区存在一些覆盖缺口。这些发现表明,在 LGG 临床试验报告和可及性方面有一些具体领域需要改进。
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
Life-Basel
Life-Basel Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
4.30
自引率
6.20%
发文量
1798
审稿时长
11 weeks
期刊介绍: Life (ISSN 2075-1729) is an international, peer-reviewed open access journal of scientific studies related to fundamental themes in Life Sciences, especially those concerned with the origins of life and evolution of biosystems. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers.
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