CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A Geographic Disparities Analysis Between Standard of Care and Clinical Trial CAR-T Patients in Kansas.
A Geographic Disparities Analysis Between Standard of Care and Clinical Trial CAR-T Patients in Kansas.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
研究结果凸显了 CAR-T 可及性方面存在重要的地域差异。
本研究比较了接受嵌合抗原受体(CAR)T细胞治疗的B细胞恶性肿瘤或多发性骨髓瘤患者的人口学和地理因素,以及堪萨斯大学癌症中心(KUCC)临床试验参与者与堪萨斯大学卫生系统(TUKHS)接受标准治疗(SOC)CAR-T 者的差异。
数据来自电子病历和KUCC临床试验管理系统。我们评估了不同种族、性别、年龄、农村居住情况及医疗专业人员短缺地区(HPSA)状态下CAR-T 治疗的可及性。SOC患者于2021年5月至2023年5月接受美国FDA批准的CAR-T;临床试验患者于2015年1月至2023年2月接受研究性CAR-T。
多数患者(80%)来自城市地区;54.1%居住在堪萨斯大学医学中心(KUMC)50英里范围内。队列中男性占58.4%,白人占86.7%,19–64岁者占60.4%,57%居住在HPSA之外。农村患者在两个队列中均占20%。临床试验组与SOC组之间未观察到显著人口学差异。然而,农村居住与年龄≥65岁(OR=1.80)、白人种族、HPSA状态以及居住地距KUMC超过50英里(OR=27.01)显著相关。HPSA状态也与居住在50英里范围之外的可能性升高相关(OR=2.29)。
研究结果凸显了CAR-T 治疗可及性方面重要的地理差异。针对农村和被指定为HPSA的社区开展定向外展,或有助于改善公平性并确保更多人获得先进疗法。
This study compares demographics and geographic factors associated with access to chimeric antigen receptor (CAR)-T cell therapy for B-cell malignancies or multiple myeloma: individuals in clinical trials at the University of Kansas Cancer Center (KUCC) and those receiving standard-of-care (SOC) CAR-T at the University of Kansas Health System (TUKHS).
Data were collected from electronic medical records and the KUCC Clinical Trial Management System. We evaluated differences in CAR-T access across race, gender, age, rurality, and HPSA status. SOC patients received FDA-approved CAR-T between May 2021 and May 2023; clinical trial patients received investigational CAR-T between January 2015 and February 2023.
Most patients (80%) were from urban areas; 54.1% lived within 50 miles of the University of Kansas Medical Center (KUMC). The cohort was 58.4% male, 86.7% white, 60.4% aged 19-64, and 57% lived outside a Health Professional Shortage Area (HPSA). Rural patients made up 20% of both cohorts. No significant demographic differences were observed between clinical trial and SOC recipients. However, rural residence was significantly associated with age 65 or older (OR = 1.80), white race, HPSA status, and living more than 50 miles from KUMC (OR = 27.01). HPSA status was also associated with greater odds of living beyond the 50-mile radius (OR = 2.29).
Findings highlight important geographic disparities in CAR-T access. Targeted outreach to rural and HPSA-designated communities may improve equity and ensure broader access to advanced therapies.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。