非小细胞肺癌生物标记物检测的真实世界订购实践:医生之间的差异及与临床结果的关联。

IF 5.3 2区 医学 Q1 ONCOLOGY
Jason M Baron, Sarrah Widatalla, Matthew A Gubens, Farah Khalil
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引用次数: 0

摘要

目的:转移性或晚期非小细胞肺癌(NSCLC)患者需要进行生物标记物检测,在大多数情况下包括无性淋巴瘤激酶(ALK)、表皮生长因子受体(EGFR)和PD-L1,以确定靶向治疗的选择,并将免疫检查点抑制剂最佳地纳入治疗方案。我们试图研究现实世界中的生物标记物检测模式,量化医生间的实践差异,并将检测与临床结果联系起来:我们从全国范围内的电子健康记录衍生的去识别数据库中提取了真实世界的数据,这些数据来自 2018 年至 2021 年期间诊断为晚期 NSCLC 并在社区环境中接受治疗的 17,165 名患者。我们使用描述性分析、固定效应和混合效应逻辑回归模型以及比例危险模型对数据进行了分析:在所有 17 165 名患者中,只有 67% 的非鳞状转移性 NSCLC 患者和 77% 的非鳞状转移性 NSCLC 患者在诊断后 90 天内进行了 ALK、EGFR 和 PD-L1 检测。较晚的诊断年份(2019-2021年与2018年相比)与较高的ALK、EGFR和PD-L1检测率有关;IIIB/C期疾病(与IV期相比)、鳞状组织学以及黑人或非裔美国人与较低的检测率有关。医生之间的差异很大,ALK、表皮生长因子受体(EGFR)和 PD-L1 检测的中位几率比(根据患者因素调整)为 1.78。如果对非鳞癌、转移性 NSCLC 患者进行所有三种生物标记物检测,他们的生存期会明显延长(所有三种生物标记物检测的中位数为 364 天,而未进行所有三种生物标记物检测的中位数为 180 天;危险比为 0.67;P < .001):结论:生物标志物检测率似乎并不理想,医生之间的差异很大。尽管本研究无法证明因果关系,但检测与生存率的提高存在相关性。需要开展更多的工作来解决导致次优检测顺序的根本原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-World Biomarker Test Ordering Practices in Non-Small Cell Lung Cancer: Interphysician Variation and Association With Clinical Outcomes.

Purpose: Patients with metastatic or advanced non-small cell lung cancer (NSCLC) need biomarker testing, including, in most cases, anaplastic lymphoma kinase (ALK), epidermal growth factor receptor (EGFR), and PD-L1, to identify options for targeted therapies and to optimally incorporate immune checkpoint inhibitors into therapeutic regimens. We sought to examine real-world patterns of biomarker testing, quantify interphysician practice variation, and correlate testing with clinical outcomes.

Methods: We extracted real-world data from a nationwide electronic health record-derived deidentified database from 17,165 patients diagnosed with advanced NSCLC between 2018 and 2021 and receiving care in the community setting. We analyzed data using descriptive analyses, fixed- and mixed-effects logistic regression models, and proportional hazard models.

Results: Only 67% of all 17,165 patients and 77% of patients with nonsquamous, metastatic NSCLC had ALK, EGFR, and PD-L1 testing within 90 days of diagnosis. Later diagnosis year (2019-2021 compared with 2018) was associated with higher rates of ALK, EGFR, and PD-L1 testing; stage IIIB/C disease (compared with stage IV), squamous histology, and Black or African American race were associated with lower rates. Interphysician variation was substantial with a median odds ratio between physicians (adjusted for patient factors) of 1.78 for ALK, EGFR, and PD-L1 testing. Patients with nonsquamous, metastatic NSCLC had significantly prolonged survival if tested with all three biomarkers (median, 364 days for all three v 180 for none of the three; hazard ratio, 0.67; P < .001).

Conclusion: Rates of biomarker testing appear suboptimal with substantial interphysician variation. Testing correlates with improved survival, although causality cannot be proven from this study. Additional work is needed to address the underlying causes of suboptimal test ordering.

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来源期刊
CiteScore
9.10
自引率
4.30%
发文量
363
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