Suppr超能文献

校准观察性健康记录数据与随机试验。

Calibrating Observational Health Record Data Against a Randomized Trial.

机构信息

Aetion, New York, New York.

Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.

出版信息

JAMA Netw Open. 2024 Sep 3;7(9):e2436535. doi: 10.1001/jamanetworkopen.2024.36535.

Abstract

IMPORTANCE

The conditions required for health record data sources to accurately assess treatment effectiveness remain unclear. Emulation of randomized clinical trials (RCTs) with health record data and subsequent calibration of the results can help elucidate this.

OBJECTIVE

To pilot an emulation of the KEYNOTE-189 RCT using a commercially available electronic health record (EHR) data source.

DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study used an EHR database spanning from April 2007 to February 2023. Follow-up began on treatment initiation and proceeded until an outcome event, loss to follow-up, end of data, or end of study period (640 days). The population-based cohort was ascertained from EHRs provided by 52 health systems across the US. Eligibility criteria were defined as closely as possible to the benchmark RCT. Patients with non-small cell lung cancer initiating first-line treatment for metastatic disease were included. Patients with evidence of squamous non-small cell lung cancer, primary nonlung malignant neoplasms, or identified EGFR/ALK variations were excluded. Data were analyzed from June to October 2023.

EXPOSURES

Initiation of first-line pembrolizumab and chemotherapy and chemotherapy alone. Chemotherapy in both groups was defined as a combination of pemetrexed and platinum-based (carboplatin or cisplatin) therapy.

MAIN OUTCOMES AND MEASURES

Outcomes of interest were 12-month survival probability and mortality hazard ratio (HR).

RESULTS

A total of 1854 patients (mean [SD] age, 63.7 [9.6] years; 971 [52.4%] men) were eligible, including 589 patients who initiated pembrolizumab and chemotherapy and 1265 patients who initiated chemotherapy only. The cohort included 364 Black patients (19.6%) and 1445 White patients (77.9%). The 12-month survival probabilities were 0.60 (95% CI, 0.54-0.65) in the pembrolizumab group and 0.58 (95% CI, 0.55-0.62) in the chemotherapy-only group, compared with 0.69 (95% CI, 0.64-0.74) in the KEYNOTE-189 pembrolizumab group and 0.49 (95% CI, 0.42-0.56) in the KEYNOTE-189 chemotherapy-only group. The mortality HR was 0.95 (95% CI, 0.78-1.16), compared with 0.49 (95% CI, 0.38-0.64) in the KEYNOTE-189 RCT.

CONCLUSIONS AND RELEVANCE

In this cohort study piloting an RCT emulation, results were incongruous with the benchmark trial. Differences in patient treatment and data capture between the RCT and EHR populations, confounding by indication, treatment crossover, and accuracy of captured diagnoses may explain these findings. Future feasibility assessments will require data sources to have important oncology-specific measures curated.

摘要

重要性

用于准确评估治疗效果的健康记录数据源所需的条件仍不清楚。使用健康记录数据模拟随机临床试验(RCT)并对结果进行校准,可以帮助阐明这一点。

目的

使用商业电子健康记录(EHR)数据源对 KEYNOTE-189 RCT 进行模拟。

设计、设置和参与者:这项回顾性队列研究使用了 2007 年 4 月至 2023 年 2 月的 EHR 数据库。随访从治疗开始开始,持续到出现结局事件、失访、数据结束或研究期结束(640 天)。该基于人群的队列是从美国 52 个卫生系统提供的 EHR 中确定的。入选标准尽可能接近基准 RCT。入组标准为患有转移性疾病的非小细胞肺癌患者,开始一线治疗。排除有鳞非小细胞肺癌、原发性非肺部恶性肿瘤或已确定 EGFR/ALK 变异的患者。数据分析于 2023 年 6 月至 10 月进行。

暴露

开始一线帕博利珠单抗和化疗以及单纯化疗。两组的化疗均定义为培美曲塞联合铂类(卡铂或顺铂)治疗。

主要结局和测量指标

感兴趣的结局是 12 个月的生存率概率和死亡率风险比(HR)。

结果

共有 1854 名患者(平均[标准差]年龄,63.7[9.6]岁;971[52.4%]名男性)符合条件,包括 589 名接受帕博利珠单抗和化疗的患者和 1265 名仅接受化疗的患者。该队列包括 364 名黑人患者(19.6%)和 1445 名白人患者(77.9%)。帕博利珠单抗组的 12 个月生存率概率为 0.60(95%置信区间,0.54-0.65),单纯化疗组为 0.58(95%置信区间,0.55-0.62),而 KEYNOTE-189 帕博利珠单抗组为 0.69(95%置信区间,0.64-0.74),KEYNOTE-189 单纯化疗组为 0.49(95%置信区间,0.42-0.56)。死亡率 HR 为 0.95(95%置信区间,0.78-1.16),而 KEYNOTE-189 RCT 为 0.49(95%置信区间,0.38-0.64)。

结论和相关性

在这项模拟 RCT 的试点队列研究中,结果与基准试验不一致。RCT 和 EHR 人群之间的患者治疗和数据采集差异、混杂因素、治疗交叉和捕获诊断的准确性可能解释了这些发现。未来的可行性评估将需要具有重要肿瘤特定措施的数据源。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验