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审查晚期前列腺癌临床试验的排除标准:对美国临床肿瘤学会和癌症研究之友的建议的评估。

Examining Exclusion Criteria in Advanced Prostate Cancer Clinical Trials: An Assessment of recommendations From the American Society Of Clinical Oncology and Friends of Cancer Research.

机构信息

Department of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA.

Department of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA; Department of Internal Medicine, Yale University School of Medicine, Yale New Haven Hospital, New Haven, CT.

出版信息

Clin Genitourin Cancer. 2023 Dec;21(6):e467-e473. doi: 10.1016/j.clgc.2023.05.013. Epub 2023 May 24.

Abstract

PURPOSE

Eligibility criteria illustrate the characteristics of the study population and promote the safety of participants. However, overreliance on restrictive eligibility criteria may limit the generalizability of outcomes. As a result, the American Society of Clinical Oncology (ASCO) and Friends of Cancer Research (Friends) issued statements to curtail these challenges. In this study, we aimed to assess restrictiveness in eligibility criteria across advanced prostate cancer clinical trials.

MATERIALS AND METHODS

We identified all phase I, II, and III advanced prostate cancer clinical trials between June 30, 2012, and June 30, 2022, through Clinicaltrials.gov. We evaluated whether a clinical trial excluded, conditionally included, or did not report 4 common criteria: brain metastases, prior or concurrent malignancies, HIV infection, and hepatitis B virus (HBV)/hepatitis C virus (HCV) infection. Performance status (PS) criteria were recorded based on the Eastern Cooperative Oncology Group (ECOG) scale.

RESULTS

Out of 699 clinical trials within our search strategy, 265 (37.9%) trials possessed all the required data and were included in our analysis. The most common excluded condition of our interest was brain metastases (60.8%), followed by HIV positivity (46.4%), HBV/HCV positivity (46.0%), and concurrent malignancies (15.5%). Additionally, 50.9% of clinical trials only included patients with ECOG PS 0 to 1. HIV and HBV/HCV infection were exclusion criteria of 22 (80.8%) and 19 (73.1%) immunotherapy trials, respectively.

CONCLUSION

Patients with brain metastases, prior or concurrent malignancies, HIV infection, HBV/HCV infection, or low-functioning PS were overly restricted from participating in advanced prostate clinical trials. Advocating for broader criteria may ameliorate generalizability.

摘要

目的

入选标准说明了研究人群的特征,并促进了参与者的安全。然而,过度依赖严格的入选标准可能会限制研究结果的普遍性。因此,美国临床肿瘤学会(ASCO)和癌症研究之友(Friends)发布了相关声明,以应对这些挑战。本研究旨在评估晚期前列腺癌临床试验入选标准的严格程度。

材料和方法

我们通过 ClinicalTrials.gov 确定了 2012 年 6 月 30 日至 2022 年 6 月 30 日期间所有 I、II 和 III 期晚期前列腺癌临床试验。我们评估了临床试验是否排除、有条件纳入或未报告 4 种常见标准:脑转移、既往或同时存在的恶性肿瘤、HIV 感染和乙型肝炎病毒(HBV)/丙型肝炎病毒(HCV)感染。体力状况(PS)标准基于东部肿瘤协作组(ECOG)量表进行记录。

结果

在我们的搜索策略中,有 699 项临床试验,其中 265 项(37.9%)试验具有所有必需的数据,并纳入我们的分析。我们感兴趣的最常见排除条件是脑转移(60.8%),其次是 HIV 阳性(46.4%)、HBV/HCV 阳性(46.0%)和同时存在的恶性肿瘤(15.5%)。此外,50.9%的临床试验仅纳入 ECOG PS 0-1 的患者。HIV 和 HBV/HCV 感染分别是 22 项(80.8%)和 19 项(73.1%)免疫治疗试验的排除标准。

结论

患有脑转移、既往或同时存在的恶性肿瘤、HIV 感染、HBV/HCV 感染或功能低下 PS 的患者被过度限制参与晚期前列腺癌临床试验。倡导更广泛的标准可能会改善普遍性。

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