评估从电子健康记录数据源得出的真实世界肿瘤反应:对接受化疗的转移性非小细胞肺癌患者进行可行性分析。

IF 3.3 Q2 ONCOLOGY
Brittany A McKelvey, Elizabeth Garrett-Mayer, Donna R Rivera, Amy Alabaster, Hillary S Andrews, Elizabeth G Bond, Thomas D Brown, Amanda Bruno, Lauren Damato, Janet L Espirito, Laura L Fernandes, Eric Hansen, Paul Kluetz, Xinran Ma, Andrea McCracken, Pallavi S Mishra-Kalyani, Yanina Natanzon, Danielle Potter, Nicholas J Robert, Lawrence Schwartz, Regina Schwind, Connor Sweetnam, Joseph Wagner, Mark D Stewart, Jeff D Allen
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引用次数: 0

摘要

目的:真实世界数据(RWD)为将真实世界(Rw)结果归因于药物干预带来了希望;然而,从 RWD 中确定治疗的 Rw 反应可能具有挑战性。癌症研究之友 "组织了一次合作,以评估与真实世界数据源中的治疗反应相关的可用数据属性,从而为捕获、定义和评估治疗反应的方法提供信息:这项回顾性非干预性(观察性)研究包括七家电子健康记录数据公司(数据提供者),它们提供了 200 名确诊为转移性非小细胞肺癌(mNSCLC)并按照共同方案接受一线铂双t化疗的患者的摘要级去标识化数据。数据提供者审查了用于评估 rw 反应(即图像、放射成像报告和临床医生反应评估)的数据组件的可用性和频率。采用通用方案评估和报告rw反应终点,包括rw反应率(rwRR)、rw反应持续时间(rwDOR),以及rw反应与rw总生存期(rwOS)、rw终止治疗时间(rwTTD)和rw下次治疗时间(rwTTNT)的关系:结果:与图像和图像报告相比,各数据集的临床医生评估的可用性和时间相对一致。使用临床医生的反应评估(可评估患者的中位比例为 77.5%)分析真实世界的反应,评估时间的一致性最高。各数据集的 rwRR(中位数为 46.5%)以及 rwOS、rwTTD 和 rwTTNT 的中位数和方向性也相对一致。不同数据集的 rwDOR 存在差异:这项合作证明了利用临床医生记录的 mNSCLC 患者的反应,整合不同数据源以评估 rw 反应终点的可行性。在评估反应和相关rw终点的数据组件的可用性方面存在异质性,需要进一步开展工作,以便在RWD来源中为药物疗效评估提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Real-World Tumor Response Derived From Electronic Health Record Data Sources: A Feasibility Analysis in Patients With Metastatic Non-Small Cell Lung Cancer Treated With Chemotherapy.

Purpose: Real-world data (RWD) holds promise for ascribing a real-world (rw) outcome to a drug intervention; however, ascertaining rw-response to treatment from RWD can be challenging. Friends of Cancer Research formed a collaboration to assess available data attributes related to rw-response across RWD sources to inform methods for capturing, defining, and evaluating rw-response.

Materials and methods: This retrospective noninterventional (observational) study included seven electronic health record data companies (data providers) providing summary-level deidentified data from 200 patients diagnosed with metastatic non-small cell lung cancer (mNSCLC) and treated with first-line platinum doublet chemotherapy following a common protocol. Data providers reviewed the availability and frequency of data components to assess rw-response (ie, images, radiology imaging reports, and clinician response assessments). A common protocol was used to assess and report rw-response end points, including rw-response rate (rwRR), rw-duration of response (rwDOR), and the association of rw-response with rw-overall survival (rwOS), rw-time to treatment discontinuation (rwTTD), and rw-time to next treatment (rwTTNT).

Results: The availability and timing of clinician assessments was relatively consistent across data sets in contrast to images and image reports. Real-world response was analyzed using clinician response assessments (median proportion of patients evaluable, 77.5%), which had the highest consistency in the timing of assessments. Relative consistency was observed across data sets for rwRR (median 46.5%), as well as the median and directionality of rwOS, rwTTD, and rwTTNT. There was variability in rwDOR across data sets.

Conclusion: This collaborative effort demonstrated the feasibility of aligning disparate data sources to evaluate rw-response end points using clinician-documented responses in patients with mNSCLC. Heterogeneity exists in the availability of data components to assess response and related rw-end points, and further work is needed to inform drug effectiveness evaluation within RWD sources.

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