Saluja Ronak, Everest Louis, Cheng Sierra, Cheung Matthew, Chan Kelvin K W
Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
JAMA Oncol. 2019 Aug 1;5(8):1188-1194. doi: 10.1001/jamaoncol.2019.0818.
The American Society of Clinical Oncology (ASCO) and the European Society for Medical Oncology (ESMO) have independently published value frameworks. To date, whether the clinical benefit scoring algorithms from these framework were intended to measure absolute or relative survival benefit remains unclear.
To empirically examine the measurement characteristics of these frameworks by comparing their survival efficacy components (ASCO clinical benefit score [CBS] and ESMO preliminary magnitude of clinical benefit grade [PMCBG]) with established measures of absolute (median survival difference and restricted mean survival time [RMST] difference) and relative (hazard ratios [HRs]) survival benefit.
The US Food and Drug Administration (FDA)'s Hematology and Oncology Approvals and Safety Notifications database was retrospectively reviewed to identify phase 3 randomized controlled trials (RCTs) cited for clinical efficacy evidence in oncology drug approvals from January 1, 2006, through December 31, 2017.
Two reviewers searched the database for initial trials cited for approval. Phase 3 trials with overall survival, progression-free survival, and/or time to progression as their primary or coprimary end points were included. Notifications for noncancer indications or presenting label changes and trials that did not report HRs for the required end points and/or did not publish survival curves with number-at-risk data were excluded. Of 269 notifications initially identified, 107 met the selection criteria.
Sensitivity analyses were conducted by calculating the scores using (1) the framework-defined end point, including tail-of-curve bonus points (ASCO) or long-term plateau adjustments (ESMO) (framework-defined end point plus tail-of-curve bonus), (2) overall survival data only, and (3) progression-free survival data only. For primary and sensitivity analyses, Spearman correlation coefficients were calculated to examine the relationships between (1) ASCO-CBS or ESMO-PMCBG and RMST difference, (2) ASCO-CBS or ESMO-PMCBG and median survival difference, and (3) ASCO-CBS or ESMO-PMCBG and HR. Data were analyzed from January 7 through April 30, 2018.
In the primary analysis, ASCO-CBSs and ESMO-PMCBGs were calculated for the included trials using the framework-defined end point.
Compared with measures of absolute survival benefit, ESMO-PMCBGs showed low to moderate correlations with RMST difference (ρ = 0.44) and moderate to high correlations with median survival difference (ρ = 0.64). ASCO-CBSs showed low to moderate correlations with both measures of absolute benefit (ρ = 0.43 for RMST difference; ρ = 0.44 for median survival). Compared with a relative measure of survival (HRs), ESMO-PMCBGs showed a low correlation (ρ = 0.47) and ASCO-CBSs showed a higher correlation (ρ = 0.76).
Neither framework consistently performed as an absolute measure of survival benefit. The incorporation of a direct measure of absolute clinical benefit, such as RMST difference, into the survival efficacy components of their algorithms should be considered.
美国临床肿瘤学会(ASCO)和欧洲医学肿瘤学会(ESMO)已分别发布了价值框架。迄今为止,这些框架中的临床获益评分算法旨在衡量绝对生存获益还是相对生存获益仍不明确。
通过将这些框架的生存疗效成分(ASCO临床获益评分 [CBS] 和ESMO临床获益初步量级分级 [PMCBG])与既定的绝对生存获益(中位生存差异和受限平均生存时间 [RMST] 差异)及相对生存获益(风险比 [HRs])测量指标进行比较,以实证检验这些框架的测量特征。
回顾性查阅美国食品药品监督管理局(FDA)的血液学和肿瘤学批准及安全通知数据库,以确定2006年1月1日至2017年12月31日期间肿瘤药物批准中引用的用于临床疗效证据的3期随机对照试验(RCT)。
两名审阅者在数据库中搜索批准引用的初始试验。纳入以总生存、无进展生存和/或疾病进展时间作为主要或共同主要终点的3期试验。排除非癌症适应症或呈现标签变更的通知以及未报告所需终点的HRs和/或未公布带有风险数数据的生存曲线的试验。在最初确定的269份通知中,107份符合选择标准。
通过使用以下方法计算得分进行敏感性分析:(1)框架定义的终点,包括曲线末端加分(ASCO)或长期平台调整(ESMO)(框架定义的终点加曲线末端加分),(2)仅总生存数据,(3)仅无进展生存数据。对于主要分析和敏感性分析,计算Spearman相关系数以检验以下各项之间的关系:(1)ASCO-CBS或ESMO-PMCBG与RMST差异,(2)ASCO-CBS或ESMO-PMCBG与中位生存差异,(3)ASCO-CBS或ESMO-PMCBG与HR。数据于2018年1月7日至4月30日进行分析。
在主要分析中,使用框架定义的终点为纳入的试验计算ASCO-CBS和ESMO-PMCBG。
与绝对生存获益测量指标相比,ESMO-PMCBG与RMST差异呈低至中度相关(ρ = 0.44),与中位生存差异呈中度至高相关(ρ = 0.64)。ASCO-CBS与两种绝对获益测量指标均呈低至中度相关(RMST差异的ρ = 0.43;中位生存的ρ = 0.44)。与相对生存测量指标(HRs)相比,ESMO-PMCBG呈低相关(ρ = 0.47),而ASCO-CBS呈较高相关(ρ = 0.76)。
两个框架均未始终如一地作为生存获益的绝对测量指标发挥作用。应考虑将绝对临床获益的直接测量指标,如RMST差异,纳入其算法的生存疗效成分中。