Department of Medical Oncology and Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Yale University School of Medicine, New Haven, CT, USA.
BJU Int. 2024 Mar;133(3):297-304. doi: 10.1111/bju.16148. Epub 2023 Sep 1.
To characterise the restrictiveness of eligibility criteria in contemporary renal cell carcinoma (RCC) trials, using recommendations from the American Society of Clinical Oncology (ASCO)-Friends of Cancer Research (FCR) initiative.
vPhase I-III trials assessing systemic therapies in patients with RCC starting between 30 June 2012 and 30 June 2022 were identified. Eligibility criteria regarding brain metastases, prior or concurrent malignancies, hepatitis B virus (HBV) or hepatitis C virus (HCV) infection, and human immunodeficiency virus (HIV) infection were identified and stratified into three groups: exclusion, conditional inclusion, and not reported. Descriptive statistics were used to determine the frequency of eligibility criteria. Fisher's exact test or chi-square test were used to calculate their associations with certain trial characteristics.
A total of 423 RCC trials were initially identified of which 112 (26.5%) had sufficient accessible information. Exclusion of patients with HIV infection, HBV/HCV infection, brain metastases, and prior or concurrent malignancies were reported in 74.1%, 53.6%, 33.0%, and 8.0% of trials, respectively. In the context of HIV and HBV/HCV infection, patients were largely excluded from trials evaluating immunotherapy (94.4% and 77.8%, respectively). In addition, brain metastases were excluded in trials assessing targeted therapy (36.4%), combined therapy (33.3%), and immunotherapy (22.2%). Exclusion of patients with prior or concurrent malignancies was less frequently reported, accounting for 9.1%, 8.3%, and 5.6% targeted therapy, combined therapy and immunotherapy trials, respectively.
A substantial proportion of RCC trials utilise restrictive eligibility criteria, excluding patients with fairly prevalent comorbidities. Implementing the ASCO-FCR recommendations will ensure resulting data are more inclusive and aligned with patient populations in the real-world.
使用美国临床肿瘤学会(ASCO)-癌症研究之友(FCR)倡议的建议,描述当代肾细胞癌(RCC)试验中纳入标准的限制性。
确定了 2012 年 6 月 30 日至 2022 年 6 月 30 日期间开始的评估 RCC 患者系统治疗的 I-III 期 v 期试验。确定并将纳入标准分为三组:排除、有条件纳入和未报告:关于脑转移、既往或同时存在恶性肿瘤、乙型肝炎病毒(HBV)或丙型肝炎病毒(HCV)感染以及人类免疫缺陷病毒(HIV)感染的纳入标准。使用描述性统计确定纳入标准的频率。Fisher 确切检验或卡方检验用于计算它们与某些试验特征的相关性。
共确定了 423 项 RCC 试验,其中 112 项(26.5%)有足够的可获取信息。分别有 74.1%、53.6%、33.0%和 8.0%的试验报告排除了 HIV 感染、HBV/HCV 感染、脑转移和既往或同时存在恶性肿瘤的患者。在 HIV 和 HBV/HCV 感染的背景下,免疫治疗试验主要排除了感染患者(分别为 94.4%和 77.8%)。此外,靶向治疗(36.4%)、联合治疗(33.3%)和免疫治疗(22.2%)试验排除了脑转移患者。既往或同时存在恶性肿瘤患者的排除率报告较少,分别占靶向治疗、联合治疗和免疫治疗试验的 9.1%、8.3%和 5.6%。
相当一部分 RCC 试验使用了限制性纳入标准,排除了相当普遍存在的合并症患者。实施 ASCO-FCR 建议将确保获得的数据更具包容性,并与真实世界中的患者群体一致。