Real-World Adherence Patterns of Comprehensive Genomic Profiling to Biomarker Recommended Therapies in Patients With Advanced Non-Small Cell Lung Cancer.

IF 4.7 3区 医学 Q1 ONCOLOGY
Rotem Ben-Shachar, Kaveri Nadhamuni, Luis E Raez, Mark Carty, Akash Mitra, Halla Nimeiri, Ira Klein, Rafi Pelossof, Daniel Morgenstzern
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Abstract

Purpose: The National Comprehensive Cancer Network (NCCN) guidelines recommend comprehensive genomic profiling (CGP) for identifying advanced non-small cell lung cancer (NSCLC) patients eligible for targeted treatment, with frequent updates to incorporate new variant-targeted therapies. CGP panels can identify multiple actionable biomarkers from a single sample to match patients to targeted therapies. We assessed the adherence rate of NCCN recommendations to variant-specific matched therapy, the impact of timing of guideline updates on adherence rates, and time from sequencing to new targeted therapy adoption.

Methods: We conducted a retrospective cohort study of stage IV NSCLC patients, with Tempus xT tissue-based sequencing. Adherence to NCCN-recommended therapy was defined as the proportion of patients who initiated guideline-directed targeted therapy when the presence of an actionable variant was identified.

Results: Among the 1,407 evaluable patients, 233 patients had a NCCN-recommended targetable variant. The treatment adherence rate was 86.3% (N = 201) with median time from sequencing to targeted therapy initiation of 23 days. A subset of adherent patients (13.4%, n = 27) had targetable variants identified prior to guideline recommendation for testing, but received matched targeted therapy within a median of 96 days of new guidelines recommendations. The variant-specific adherence rate was correlated with the timing of guideline recommendation (P = .02, Wald test), with lower adherence rates for variant-matched therapies recently included into guidelines.

Conclusion: In a large, real-world cohort of advanced NSCLC patients tested with CGP, the treatment adherence rate to matched NCCN-recommended targeted therapy was high. This study highlights the importance of CGP testing in identifying variants to provide timely matched targeted therapy in a rapidly evolving biomarker and therapeutic landscape.

晚期非小细胞肺癌患者对生物标志物推荐疗法的综合基因组分析的真实世界依从性模式
目的:国家综合癌症网络(NCCN)指南推荐综合基因组谱分析(CGP)来识别符合靶向治疗条件的晚期非小细胞肺癌(NSCLC)患者,并经常更新以纳入新的变异靶向治疗。CGP面板可以从单个样本中识别多个可操作的生物标志物,以匹配患者的靶向治疗。我们评估了NCCN推荐的不同特异性匹配治疗的依从率,指南更新时间对依从率的影响,以及从测序到采用新靶向治疗的时间。方法:我们对IV期非小细胞肺癌患者进行了回顾性队列研究,采用基于Tempus xT组织的测序。nccn推荐治疗的依从性定义为当确定存在可操作的变异时,启动指南指导的靶向治疗的患者比例。结果:在1407例可评估的患者中,233例患者具有nccn推荐的靶向变异。治疗依从率为86.3% (N = 201),从测序到靶向治疗开始的中位时间为23天。一部分患者(13.4%,n = 27)在指南推荐检测之前已发现可靶向变异,但在新指南推荐的中位96天内接受了匹配的靶向治疗。变异特异性依从率与指南推荐的时间相关(P = 0.02, Wald检验),最近纳入指南的变异匹配疗法的依从率较低。结论:在接受CGP测试的大型现实世界晚期NSCLC患者队列中,匹配nccn推荐的靶向治疗的治疗依从率很高。这项研究强调了CGP检测在识别变异方面的重要性,在快速发展的生物标志物和治疗领域提供及时匹配的靶向治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
7.50%
发文量
518
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