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评估评估系统治疗评估系统治疗的肾细胞癌试验的资格标准。

Assessment of eligibility criteria in renal cell carcinoma trials evaluating systemic therapy.

机构信息

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.

出版信息

BJU Int. 2024 Mar;133(3):297-304. doi: 10.1111/bju.16148. Epub 2023 Sep 1.

Abstract

OBJECTIVES

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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%。

结论

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。

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