University of Granada, Granada, Spain.
Department of Pharmacy, Catalan Institute of Oncology, L'Hospitalet de Llobregat, Barcelona, Spain.
Acta Oncol. 2021 Sep;60(9):1225-1232. doi: 10.1080/0284186X.2021.1942546. Epub 2021 Jun 29.
Despite newer therapies, advanced or metastatic non-small-cell lung cancer (NSCLC) continues to be the leading cause of cancer-related deaths worldwide. Deficits in the design and methods of randomized controlled trials (RCTs) may contribute to reducing the clinical benefit of therapies in oncology. To prioritize treatments based on efficacy results and toxicity data, the (ESMO) has developed the Magnitude of Clinical Benefit Scale (MCBS). The objective of this study was to apply the ESMO-MCBS v1.1 to a cohort of RCTs on therapies for advanced or metastatic NSCLC.
Phase III and pivotal phase II trials, published between 2013 and 2018, investigating drug therapies for advanced NSCLC were included. was specifically searched for efficacy/toxicity updates. Treatments were graded 5 to 1 on the ESMO-MCBS v1.1, using the lower limit of the 95% confidence interval of the hazard ratio (HR), where scores 5 and 4 represent a substantial clinical benefit. Additionally, scores using the point estimate HR were generated, for comparison. Discrepancies between our grade estimations and the ones published on the ESMO website, as scorecards, were identified.
ESMO-MCBS scores were calculated for 42 positive clinical trials. 54.8% met the ESMO-MCBS thresholds for clinically meaningful benefit (final grade of 4 or 5). That percentage decreased to 40.5% when considering the point estimate of the HR. 50.0% of the trials had no published scorecard on the ESMO website and discrepancies affected 11 (26.2%) studies.
Almost half of the RCTs showing a statistically significant result favoring the experimental arm, failed to demonstrate a substantial clinical benefit according to the ESMO framework.
尽管有更新的疗法,晚期或转移性非小细胞肺癌(NSCLC)仍然是全球癌症相关死亡的主要原因。随机对照试验(RCT)的设计和方法上的缺陷可能导致肿瘤学治疗的临床获益降低。为了根据疗效结果和毒性数据优先考虑治疗方法,欧洲肿瘤内科学会(ESMO)制定了临床获益幅度量表(MCBS)。本研究的目的是将 ESMO-MCBS v1.1 应用于一组晚期或转移性 NSCLC 治疗的 RCT 队列。
纳入了 2013 年至 2018 年期间发表的 III 期和关键 II 期试验,研究药物治疗晚期 NSCLC 的疗效/毒性更新情况。专门在 上搜索了疗效/毒性更新。使用风险比(HR)的 95%置信区间下限对 ESMO-MCBS v1.1 进行治疗评分,评分 5 和 4 表示具有显著的临床获益。此外,还生成了使用点估计 HR 的评分,用于比较。确定了我们的分级估计与 ESMO 网站上发布的评分卡之间的差异。
对 42 项阳性临床试验进行了 ESMO-MCBS 评分。54.8%的试验符合 ESMO-MCBS 临床有意义获益的阈值(最终评分 4 或 5)。当考虑 HR 的点估计时,这一比例下降到 40.5%。50.0%的试验在 ESMO 网站上没有发布评分卡,差异影响了 11 项(26.2%)研究。
显示有利于实验组的统计学显著结果的 RCT 中,近一半未能根据 ESMO 框架证明具有显著的临床获益。