非小细胞肺癌治疗后监测指南的依从性:回顾性队列研究。

IF 2.7 Q2 ONCOLOGY
JMIR Cancer Pub Date : 2025-10-01 DOI:10.2196/76515
Ryan J Randle, Scott V Adams, Zahra Esfahanimonfared, Nicole Lin, Julie Wu, Ann Leung, Steven M Asch, Steven Zeliadt, Alex Sox-Harris, Summer Han, Leah M Backhus
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引用次数: 0

摘要

背景:一些指南建议对非小细胞肺癌(NSCLC)进行治疗后监测。然而,评估监测模式的研究往往不能区分为监测而安排的影像学与提示复发的症状。此外,早期复发和其他竞争事件阻碍了确定真正监测率的努力,因为在临床实践中报告的指南依从性存在很大差异。利用退伍军人健康管理局的综合数据,我们开发了一个新的竞争风险框架来描述非小细胞肺癌成像监测的模式和预测因素。目的:本研究旨在检查治疗后监测,以估计早期NSCLC患者指南一致性护理的真实监测率和预测因素。方法:研究队列包括2008年至2016年期间接受1至3期NSCLC治疗且存活≥6个月的退伍军人。对临床文献和影像学报告进行摘要,以获取影像指征和临床信息。我们估计了在治疗后4至9个月内接受符合指南的监测的累积概率,定义为胸部计算机断层扫描成像,考虑了竞争风险和审查。多变量病因特异性Cox回归用于估计患者因素与指南一致性监测之间的关联,并对多重比较进行调整。结果:该队列包括1888例患者。分析队列的平均年龄为66.4岁(SD 7.9);男性占95.9%(1811/1888),白人占71.1%(1342/1888),已婚占43.1%(814/1888)。在1888例患者中,57% (n=1076)表现为1期疾病,最常见的治疗方式是单纯手术(n=1068, 56.6%)。在最初的120- 270天窗口期,最常见的影像学检查是胸部计算机断层扫描(1460/3278,44.5%)。胸部x线占所有影像学检查的36.3%(1190/3278),其余11.8%(386/3278)和7.4%(242/3278)分别为正电子发射断层扫描或其他影像学检查。与2008年至2010年相比,2014年至2016年接受非小细胞肺癌治疗的患者接受指南一致性监测的可能性显著增加(风险比1.42)。结论:在这种独特的竞争风险框架应用中,该国家队列的指南一致性监测率低于许多先前研究的报道。这一发现突出了在符合条件的无症状肺癌幸存者中监测的潜在巨大差距。需要更多的战略来衡量符合指南的监测的真实比率,以及教育和宣传,以确保符合指南的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adherence to Posttreatment Surveillance Guidelines in Non-Small Cell Lung Cancer: Retrospective Cohort Study.

Background: Several guidelines recommend posttreatment surveillance for non-small cell lung cancer (NSCLC). However, studies evaluating surveillance patterns often cannot distinguish between imaging ordered for surveillance versus for symptoms suggestive of recurrence. Moreover, early recurrences and other competing events hamper efforts to determine true surveillance rates because of wide variability in reported guideline adherence in clinical practice. Leveraging comprehensive Veterans Health Administration data, we developed a novel competing risks framework to describe the patterns and predictors of NSCLC imaging surveillance.

Objective: This study aims to examine posttreatment surveillance to estimate the true surveillance rates and predictors of guideline-concordant care in patients with early-stage NSCLC.

Methods: The study cohort comprised veterans who were treated for stage 1 to 3 NSCLC between 2008 and 2016 and who survived for ≥6 months. Clinical documents and radiology reports were abstracted for image indication and clinical information. We estimated the cumulative probability of receiving guideline-concordant surveillance, defined as chest computed tomography imaging within 4 to 9 months after treatment, accounting for competing risks and censoring. Multivariable cause-specific Cox regression was used to estimate associations between patient factors and guideline-concordant surveillance, with adjustments made for multiple comparisons.

Results: The cohort consisted of 1888 patients. The mean age of the analysis cohort was 66.4 (SD 7.9) years; 95.9% (1811/1888) of the patients were male, 71.1% (1342/1888) of the patients were White, and 43.1% (814/1888) were married. Of the 1888 patients, 57% (n=1076) presented with stage 1 disease, and the most common treatment modality was surgery alone (n=1068, 56.6%). The most common type of imaging performed during the initial 120- to 270-day window was chest computed tomography (1460/3278, 44.5%). Chest X-rays accounted for 36.3% (1190/3278) of all imaging performed, while the remaining 11.8% (386/3278) and 7.4% (242/3278) were positron emission tomography scans or other imaging modalities, respectively. Compared to the years 2008 to 2010, patients treated for NSCLC from 2014 to 2016 had a significantly higher likelihood of receiving guideline-concordant surveillance (hazard ratio 1.42, P<.001).

Conclusions: In this unique application of a competing risks framework, the rate of guideline-concordant surveillance in this national cohort was lower than that reported in many previous studies. This finding highlights a potentially substantial gap in surveillance among eligible, asymptomatic lung cancer survivors. More strategies are needed to measure the true rate of guideline-concordant surveillance, along with education and advocacy to ensure guideline-concordant care.

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来源期刊
JMIR Cancer
JMIR Cancer ONCOLOGY-
CiteScore
4.10
自引率
0.00%
发文量
64
审稿时长
12 weeks
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