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德克萨斯州免疫疗法在非小细胞肺癌中的应用模式:监管批准前后。

Patterns of immunotherapy utilization for non-small cell lung cancer in Texas pre- and post-regulatory approval.

机构信息

Department of Pharmaceutical Health Outcomes and Policy, College of Pharmacy, University of Houston, Health 2, Room 4050, 4349 Martin Luther King Boulevard, Houston, TX, 77204-5047, USA.

出版信息

Clin Transl Oncol. 2024 Aug;26(8):1908-1920. doi: 10.1007/s12094-024-03412-9. Epub 2024 Mar 30.

Abstract

PURPOSE

Immunotherapy has shown remarkable benefits for non-small cell lung cancer (NSCLC) since approved by the US Food and Drug Administration (FDA). Texas, however, ranks below the national average in access to treatment for NSCLC. This retrospective cohort study assessed first-line immunotherapy treatment patterns and associated factors pre- and post-FDA approval in Texas.

METHODS

Patients ≥18 years diagnosed with NSCLC from the Texas Cancer Registry database (2011-2018) and were stratified into pre- and post-FDA approval era. The rates of immunotherapy utilization were examined, and the average annual percent change (AAPC) in immunotherapy utilization across patient subgroups was compared. Multivariable logistic regression was used to identify associations of patient characteristics with immunotherapy utilization for patients with metastatic- and all-stage NSCLC.

RESULTS

A total of 13,501 and 9509 patients with NSCLC were identified in pre-post-approval periods, respectively. Post-approval, immunotherapy utilization increased from 1.7 to 13.0%, and AAPC from 54.8 to 82.7%. Pre-approval, patients living in a county with ≥20% of households below the poverty level were less likely to receive immunotherapy (OR = 0.73, 95% CI = 0.61-0.94) while patients with private insurance were more likely to receive immunotherapy (OR = 1.56, 95% CI = 1.10-2.23). Post-approval, socioeconomic disparities were more prominent (10-19.9 and ≥20% of households below the poverty level: OR = 0.77, 95% CI = 0.66-0.90 and OR = 0.71, 95% CI = 0.60-0.86, respectively). Patients with metastatic NSCLC showed similar patterns of socioeconomic disparities pre- and post-approval.

CONCLUSIONS

Our findings suggest that patients' socioeconomic status hinders immunotherapy utilization for NSCLC in Texas. This emphasizes the need for state health policy reforms such as Medicaid expansion and tailored cancer care strategies.

摘要

目的

自美国食品和药物管理局(FDA)批准免疫疗法以来,它已显示出对非小细胞肺癌(NSCLC)的显著益处。然而,得克萨斯州在 NSCLC 治疗的可及性方面排名低于全国平均水平。这项回顾性队列研究评估了在 FDA 批准前后,得克萨斯州 NSCLC 患者一线免疫治疗模式及其相关因素。

方法

从德克萨斯癌症登记数据库(2011-2018 年)中筛选出年龄≥18 岁的 NSCLC 患者,并将其分为 FDA 批准前和批准后两个时期。检查免疫治疗的使用率,并比较各亚组患者免疫治疗使用率的年平均百分比变化(AAPC)。多变量逻辑回归用于确定转移性和所有阶段 NSCLC 患者的人口统计学特征与免疫治疗使用率的相关性。

结果

分别有 13501 例和 9509 例 NSCLC 患者被纳入批准前和批准后时期。批准后,免疫治疗的使用率从 1.7%增加到 13.0%,AAPC 从 54.8%增加到 82.7%。在批准前,居住在家庭贫困率≥20%的县的患者接受免疫治疗的可能性较低(OR=0.73,95%CI=0.61-0.94),而拥有私人保险的患者接受免疫治疗的可能性较高(OR=1.56,95%CI=1.10-2.23)。批准后,社会经济差距更加明显(家庭贫困率为 10%-19.9%和≥20%:OR=0.77,95%CI=0.66-0.90 和 OR=0.71,95%CI=0.60-0.86)。转移性 NSCLC 患者在批准前后也表现出类似的社会经济差异模式。

结论

我们的研究结果表明,得克萨斯州患者的社会经济地位阻碍了 NSCLC 的免疫治疗。这强调了州卫生政策改革的必要性,如医疗补助扩大和量身定制的癌症护理策略。

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