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在涉及免疫疗法的膀胱癌临床试验中研究患者特征。

Examining Patient Characteristics in Bladder Cancer Clinical Trials Involving Immunotherapy.

作者信息

Ikhapoh Izuagie, Atairu Usomine, Reich Amanda Jane, Mantia Charlene M, Wei Xiao X, Sekar Rishi, Clinton Timothy N, Mossanen Matthew

机构信息

Department of Medical Science, Harvard Medical School, Boston, MA 02115, USA.

Department of Medical Microbiology and Immunology, Creighton School of Medicine, Omaha, NE 68178, USA.

出版信息

J Clin Med. 2025 Jan 29;14(3):879. doi: 10.3390/jcm14030879.

Abstract

: Comprehending the patient composition of bladder cancer (BC) clinical trials is crucial for effectively designing clinical trials and contextualizing the generated science. In this study, we reviewed publicly available data and explored the demographic information of BC studies administering immune checkpoint inhibitors (ICIs). : Trial eligibility was irrespective of government or private sponsorship, and trial activation dates were limited to between 2013 and 2023. The main inclusion criteria were use of ICIs and trials reporting endpoints that include progression-free survival (PFS), overall survival (OS), disease-free survival (DFS), and event-free survival (EFS). The key exclusion terms were review articles and meta-analysis. : We identified a total of 109 clinical trials with an aggregate total of 8936 enrolled patients. Ninety-six percent identified as Caucasian or White European, and 23% identified as female. Further analyses revealed that 65% of the patients were aged 65 years or older. One-third of the trials listed similar comorbidities, such as cardiovascular disease and diabetes, that were exhibited by approximately 30 percent of the patients. : Our data suggest that recruitment strategies should be mindful of comorbidities that may interfere with ICI treatments. Additionally, our results are consistent with findings from other reviews that indicate that certain patient groups may be under-represented in BC trials.

摘要

了解膀胱癌(BC)临床试验的患者构成对于有效设计临床试验以及将所产生的科学成果置于具体情境中至关重要。在本研究中,我们回顾了公开可用的数据,并探究了使用免疫检查点抑制剂(ICI)的BC研究的人口统计学信息。:试验资格不受政府或私人赞助的影响,试验启动日期限于2013年至2023年之间。主要纳入标准是使用ICI以及报告包括无进展生存期(PFS)、总生存期(OS)、无病生存期(DFS)和无事件生存期(EFS)等终点的试验。关键排除术语是综述文章和荟萃分析。:我们共确定了109项临床试验,总计有8936名入组患者。96%的患者被确定为白种人或欧洲白人,23%的患者被确定为女性。进一步分析显示,65%的患者年龄在65岁及以上。三分之一的试验列出了类似的合并症,如心血管疾病和糖尿病,约30%的患者患有这些疾病。:我们的数据表明,招募策略应考虑到可能干扰ICI治疗的合并症。此外,我们的结果与其他综述的结果一致,这些综述表明某些患者群体在BC试验中的代表性可能不足。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5428/11818695/8a700785f2c3/jcm-14-00879-g001.jpg

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