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Current status and perspectives of interventional clinical trials for glioblastoma – analysis of ClinicalTrials.gov

机译:胶质母细胞瘤介入临床试验的现状与展望– ClinicalTrials.gov分析

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摘要

The records of 208.777 (100%) clinical trials registered at ClinicalTrials.gov were downloaded on the 19th of February 2016. Phase II and III trials including patients with glioblastoma were selected for further classification and analysis. Based on the disease settings, trials were classified into three groups: newly diagnosed glioblastoma, recurrent disease and trials with no differentiation according to disease setting. Furthermore, we categorized trials according to the experimental interventions, the primary sponsor, the source of financial support and trial design elements. Trends were evaluated using the autoregressive integrated moving average model. Two hundred sixteen (0.1%) trials were selected for further analysis. Academic centers (investigator initiated trials) were recorded as primary sponsors in 56.9% of trials, followed by industry 25.9%. Industry was the leading source of monetary support for the selected trials in 44.4%, followed by 25% of trials with primarily academic financial support. The number of newly initiated trials between 2005 and 2015 shows a positive trend, mainly through an increase in phase II trials, whereas phase III trials show a negative trend. The vast majority of trials evaluate forms of different systemic treatments (91.2%). In total, one hundred different molecular entities or biologicals were identified. Of those, 60% were involving drugs specifically designed for central nervous system malignancies. Trials that specifically address radiotherapy, surgery, imaging and other therapeutic or diagnostic methods appear to be rare. Current research in glioblastoma is mainly driven or sponsored by industry, academic medical oncologists and neuro-oncologists, with the majority of trials evaluating forms of systemic therapies. Few trials reach phase III. Imaging, radiation therapy and surgical procedures are underrepresented in current trials portfolios. Optimization in research portfolio for glioblastoma is needed.Electronic supplementary materialThe online version of this article (doi:10.1186/s13014-016-0740-5) contains supplementary material, which is available to authorized users.
机译:2016年2月19日下载了ClinicalTrials.gov上注册的208.777(100%)个临床试验的记录。选择了包括胶质母细胞瘤患者在内的II期和III期试验以进行进一步的分类和分析。根据疾病情况,将试验分为三类:新诊断的胶质母细胞瘤,复发性疾病和根据疾病背景无差异的试验。此外,我们根据实验干预措施,主要赞助者,资金支持来源和试验设计要素对试验进行了分类。使用自回归综合移动平均模型评估趋势。选择了116个(0.1%)试验进行进一步分析。学术中心(由研究人员发起的试验)在试验中占56.9%为主要发起人,其次是行业,为25.9%。在选定的试验中,工业是获得金钱支持的主要来源,占44.4%,其次是25%的试验,主要是学术上的财政支持。在2005年至2015年之间,新启动的试验数量呈积极趋势,主要是通过增加II期试验,而III期试验则呈负趋势。绝大多数试验评估了不同全身治疗的形式(91.2%)。总共鉴定出一百种不同的分子实体或生物。其中,60%涉及专门为中枢神经系统恶性肿瘤设计的药物。专门针对放射疗法,手术,影像学和其他治疗或诊断方法的试验似乎很少。目前关于胶质母细胞瘤的研究主要由行业,学术医学肿瘤学家和神经肿瘤学家驱动或赞助,大多数试验评估全身疗法的形式。很少有试验达到第三阶段。影像,放射治疗和手术程序在当前的试验产品组合中代表性不足。电子补充材料本文的在线版本(doi:10.1186 / s13014-016-0740-5)包含补充材料,授权用户可以使用。

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