Tang Monica, Lee Chee K, Lewis Craig R, Boyer Michael, Brown Bernadette, Schaffer Andrea, Pearson Sallie-Anne, Simes Robert J
Centre for Big Data Research in Health, University of New South Wales, Level 2, AGSM Building (G27), UNSW Sydney, NSW 2052, Australia.
NHMRC Clinical Trials Centre, University of Sydney, Levels 4-6 Medical Foundation Building, 92-94 Parramatta Rd, Camperdown, NSW 2050, Australia.
Lung Cancer. 2022 Apr;166:40-48. doi: 10.1016/j.lungcan.2022.01.024. Epub 2022 Feb 3.
Based on data from randomized controlled trials (RCTs), immune checkpoint inhibitors (ICI) are standard-of-care in advanced non-small cell lung cancer (aNSCLC). However, trial eligibility criteria are restrictive, and participants and outcomes may not represent the wider population. We aim to assess the generalizability of key phase III RCTs to real-world patients.
Among aNSCLC patients enrolled in the Embedding Research (and Evidence) in Cancer Healthcare (EnRICH) program between 26/6/17-18/2/21, we assessed the proportion of patients who fulfilled key trial eligibility criteria: performance status (PS) 0-1, normal laboratory results, no EGFR/ALK mutations, no exclusionary comorbidities (previous cancer, conditions necessitating steroid use, autoimmune diseases, HIV, hepatitis B/C, tuberculosis, interstitial lung disease, organ transplantation). We defined patients who met all assessed criteria as trial-typical and describe ICI uptake and overall survival (OS).
Of 454 patients (median age 71 years, 42.1% female), 30% were trial-typical. Less than half received ICI (47.6%), with trial-typical patients more likely to receive ICI (69.1% vs 38.4%, adjusted odds ratio 3.77, 95% CI 2.40-5.91). Median OS was 10.2 and 5.4 months in patients receiving first- and second-line ICI, respectively. Rationalizing trial criteria to include patients with PS ≤ 2 and exclude those with targetable mutations, steroid use, autoimmune diseases, interstitial lung disease, tuberculosis or organ transplantation increased the proportion of trial-typical patients to 57.3%.
Landmark phase III RCTs in aNSCLC have limited generalizability. OS of real-world patients receiving ICI is shorter than reported in trials. Novel ICI trials should consider broader eligibility criteria to improve their generalizability.
基于随机对照试验(RCT)的数据,免疫检查点抑制剂(ICI)是晚期非小细胞肺癌(aNSCLC)的标准治疗方法。然而,试验纳入标准具有局限性,参与者和结果可能无法代表更广泛的人群。我们旨在评估关键的III期RCT对真实世界患者的可推广性。
在2017年6月26日至2021年2月18日期间纳入癌症医疗保健中的嵌入研究(和证据)(EnRICH)项目的aNSCLC患者中,我们评估了符合关键试验纳入标准的患者比例:体能状态(PS)为0-1、实验室检查结果正常、无EGFR/ALK突变、无排除性合并症(既往癌症、需要使用类固醇的疾病、自身免疫性疾病、HIV、乙型/丙型肝炎、结核病、间质性肺病、器官移植)。我们将符合所有评估标准的患者定义为试验典型患者,并描述ICI的使用情况和总生存期(OS)。
在454例患者(中位年龄71岁,42.1%为女性)中,30%为试验典型患者。不到一半的患者接受了ICI(47.6%),试验典型患者更有可能接受ICI(69.1%对38.4%,调整后的优势比为3.77,95%CI为2.40-5.91)。接受一线和二线ICI的患者的中位OS分别为10.2个月和5.4个月。将试验标准合理化,纳入PS≤2的患者,并排除具有可靶向突变、使用类固醇、自身免疫性疾病、间质性肺病、结核病或器官移植的患者,可使试验典型患者的比例增加至57.3%。
aNSCLC的标志性III期RCT的可推广性有限。接受ICI的真实世界患者的OS比试验中报告的要短。新的ICI试验应考虑更广泛的纳入标准,以提高其可推广性。