Xu Emily, Patterson Jonathan, Angione Angelo, Li Alexander, Wu David W, Akca Ebrar, Elghawy Omar, Barsouk Alexander, Sussman Jonathan H
Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, 3401 Civic Center Blvd., Philadelphia, PA 19104, USA.
Graduate Group in Genomics and Computational Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Life (Basel). 2024 Sep 9;14(9):1133. doi: 10.3390/life14091133.
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.
低级别胶质瘤(LGG)是一种中枢神经系统恶性肿瘤,通常可通过手术切除和放化疗进行治疗。然而,尽管对标准治疗最初有积极反应,但大多数LGG最终会进展为高级别胶质瘤,而高级别胶质瘤几乎无一例外都是致命的。迫切需要更多的临床试验以及更高的临床试验可及性,以改善LGG的治疗标准来延缓或预防其进展。在本研究中,我们系统地审查了美国开展的LGG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年在ClinicalTrials.gov上注册的已完成LGG试验的试验设计趋势以及报告的人口统计学数据。对纳入标准、研究性治疗、主要结局和初步结果进行了比较和总结。该研究共纳入了14项试验,1067名参与者。大多数试验并非仅针对LGG,14%的试验有特定突变的纳入标准。迄今为止,其中两项试验已带来了美国食品药品监督管理局(FDA)批准的新治疗方法。所有试验都报告了年龄和性别,而只有57%报告了种族,43%报告了族裔。自我认定为黑人或非裔美国人以及亚裔或太平洋岛民的个体在统计学上代表性不足。最后我们调查了美国各地试验点的地理分布,结果显示落基山脉地区和东南部地区存在若干覆盖空白。这些发现表明了LGG临床试验报告和可及性方面需要改进的具体领域。