基于电子病历的督促干预增加转移性非小细胞肺癌患者的综合分子基因分型:一项前瞻性临床试验的结果。

IF 4.7 3区 医学 Q1 ONCOLOGY JCO oncology practice Pub Date : 2024-07-03 DOI:10.1200/OP.24.00070
Melina E Marmarelis, Dylan G Scholes, Tara L McWilliams, Wei-Ting Hwang, John Kosteva, Michael R Costello, Lova Sun, Aditi P Singh, Kelsey S Lau-Min, Abigail Doucette, Peter E Gabriel, Anthony O Martella, Megan A Roy, Jeffrey C Thompson, Roger B Cohen, David W Dougherty, Lawrence N Shulman, Corey J Langer, Justin E Bekelman, Erica L Carpenter, Charu Aggarwal
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引用次数: 0

摘要

目的:不到一半的新诊断转移性非小细胞肺癌(NSCLC)患者接受了全面的分子检测。我们设计了一种基于电子病历(EMR)的 "提示干预",在肿瘤内科初诊时提示患者进行血浆分子检测:方法:在宾夕法尼亚大学的学术实践和两个附属社区实践中开展了一项非随机前瞻性试验。通过组织和/或血浆新一代测序方法进行分子基因分型。全面检测的定义是对 EGFR、ALK、BRAF、ROS1、MET、RET、KRAS 和 NTRK 进行检测。根据美国国立综合癌症网络(NCCN)指南,与指南一致的治疗定义为使用适当的一线(1L)疗法。使用费舍尔精确检验或皮尔逊卡方检验比较干预前和干预后组群中随时可获得综合分子基因分型结果、1L 治疗前可获得分子结果和指南一致的 1L 治疗的患者比例:共纳入 533 名患者,其中干预前队列中有 376 人,干预后队列中有 157 人。在实施基于电子病历的干预后,干预后队列中接受全面分子检测的患者比例高于干预前队列(100% 对 88%,P = 对 91.6%,P = .026),接受 NCCN 指南一致性治疗的患者比例也高于干预前队列(89.8% 对 78.2%,P = .035):结论:在一个大型医疗系统的三个医疗点中,实施以医疗服务团队为中心、基于EMR的劝导干预是可行的,并使更多的NSCLC患者接受了全面的分子基因分型。这些研究结果表明,行为劝导可以促进分子检测,应将其作为一种工具进一步研究,以改善社区和学术机构的指南一致性护理。
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Electronic Medical Record-Based Nudge Intervention to Increase Comprehensive Molecular Genotyping in Patients With Metastatic Non-Small Cell Lung Cancer: Results From a Prospective Clinical Trial.

Purpose: Less than half of the patients with newly diagnosed metastatic non-small cell lung cancer (NSCLC) undergo comprehensive molecular testing. We designed an electronic medical record (EMR)-based "nudge intervention" to prompt plasma-based molecular testing at the time of initial medical oncology consultation.

Methods: A nonrandomized prospective trial was conducted at the University of Pennsylvania's academic practice and two affiliated community practices. Molecular genotyping was performed by tissue- and/or plasma-based next generation sequencing methods. Comprehensive testing was defined as testing for EGFR, ALK, BRAF, ROS1, MET, RET, KRAS, and NTRK. Guideline-concordant treatment was defined as the use of the appropriate first-line (1L) therapy as per the National Comprehensive Cancer Network (NCCN) guidelines. Proportion of patients with comprehensive molecular genotyping results available at any time, molecular results available before 1L therapy, and guideline-concordant 1L treatment were compared between the preintervention and postintervention cohorts using Fisher's exact test or Pearson's chi-squared test.

Results: Five hundred and thirty-three patients were included, 376 in the preintervention cohort and 157 in the postintervention cohort. After implementation of the EMR-based nudge, a higher proportion of patients underwent comprehensive molecular testing in the postintervention versus the preintervention cohort (100% v 88%, P = <.001), had results of comprehensive molecular testing available before initiating 1L treatment (97.3% v 91.6%, P = .026), and received NCCN guideline-concordant care (89.8% v 78.2%, P = .035).

Conclusion: Across three practice sites in a large health system, implementation of a provider team-focused EMR-based nudge intervention was feasible, and led to a higher number of patients with NSCLC undergoing comprehensive molecular genotyping. These findings demonstrate that behavioral nudges can promote molecular testing and should be studied further as a tool to improve guideline-concordant care in both community and academic sites.

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