Stewart Mark, Norden Andrew D, Dreyer Nancy, Henk Henry Joe, Abernethy Amy P, Chrischilles Elizabeth, Kushi Lawrence, Mansfield Aaron S, Khozin Sean, Sharon Elad, Arunajadai Srikesh, Carnahan Ryan, Christian Jennifer B, Miksad Rebecca A, Sakoda Lori C, Torres Aracelis Z, Valice Emily, Allen Jeff
Friends of Cancer Research, Washington, DC.
Cota Healthcare, New York, NY.
JCO Clin Cancer Inform. 2019 Jul;3:1-15. doi: 10.1200/CCI.18.00155.
This pilot study examined the ability to operationalize the collection of real-world data to explore the potential use of real-world end points extracted from data from diverse health care data organizations and to assess how these relate to similar end points in clinical trials for immunotherapy-treated advanced non-small-cell lung cancer.
Researchers from six organizations followed a common protocol using data from administrative claims and electronic health records to assess real-world end points, including overall survival (rwOS), time to next treatment, time to treatment discontinuation (rwTTD), time to progression, and progression-free survival, among patients with advanced non-small-cell lung cancer treated with programmed death 1/programmed death-ligand 1 inhibitors in real-world settings. Data sets included from 269 to 6,924 patients who were treated between January 2011 and October 2017. Results from contributors were anonymized.
Correlations between real-world intermediate end points (rwTTD and time to next treatment) and rwOS were moderate to high (range, 0.6 to 0.9). rwTTD was the most consistent end points as treatment detail was available in all data sets. rwOS at 1 year post-programmed death-ligand 1 initiation ranged from 40% to 57%. In addition, rwOS as assessed via electronic health records and claims data fell within the range of median OS values observed in relevant clinical trials. Data sources had been used extensively for research with ongoing data curation to assure accuracy and practical completeness before the initiation of this research.
These findings demonstrate that real-world end points are generally consistent with each other and with outcomes observed in randomized clinical trials, which substantiates the potential validity of real-world data to support regulatory and payer decision making. Differences observed likely reflect true differences between real-world and protocol-driven practices.
本初步研究考察了实施真实世界数据收集的能力,以探索从不同医疗保健数据组织的数据中提取的真实世界终点的潜在用途,并评估这些终点与免疫治疗的晚期非小细胞肺癌临床试验中类似终点的关系。
来自六个组织的研究人员遵循通用方案,使用行政索赔数据和电子健康记录来评估真实世界终点,包括总生存期(rwOS)、下次治疗时间、治疗中断时间(rwTTD)、疾病进展时间和无进展生存期,这些终点来自于在真实世界环境中接受程序性死亡1/程序性死亡配体1抑制剂治疗的晚期非小细胞肺癌患者。数据集包括2011年1月至2017年10月期间接受治疗的269至6924名患者。各贡献者的结果均进行了匿名处理。
真实世界中间终点(rwTTD和下次治疗时间)与rwOS之间的相关性为中度至高度(范围为0.6至0.9)。rwTTD是最一致的终点,因为所有数据集中都有治疗细节。程序性死亡配体1开始治疗后1年的rwOS范围为40%至57%。此外,通过电子健康记录和索赔数据评估的rwOS落在相关临床试验中观察到的中位OS值范围内。在本研究开始之前,数据源已广泛用于研究,并进行了持续的数据整理以确保准确性和实际完整性。
这些发现表明,真实世界终点通常彼此一致,并且与随机临床试验中观察到的结果一致,这证实了真实世界数据支持监管和支付方决策的潜在有效性。观察到的差异可能反映了真实世界实践与方案驱动实践之间的真正差异。