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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Sociodemographic Factors Influencing Access to Chimeric Antigen T-Cell Receptor Therapy for Patients With Non-Hodgkin Lymphoma.
Sociodemographic Factors Influencing Access to Chimeric Antigen T-Cell Receptor Therapy for Patients With Non-Hodgkin Lymphoma.
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我们的研究表明,CAR-T 治疗可以跨越社会人口学障碍实施,并凸显了考虑健康的社会决定因素以优化所有患者可及性的重要性。
目前已有CAR-T 细胞疗法用于非霍奇金淋巴瘤(NHL)患者,但与疾病无关的因素限制了其可及性。
我们开展回顾性研究,评估社会人口学因素对本院 2016 至 2023 年接受 CAR-T 治疗的成人 B 细胞 NHL 患者治疗可及性和结局的影响。
154 例接受 CAR-T 治疗患者中,43% 年龄超过 65 岁,68% 为男性,14% 为非白人(包括西班牙裔)。65 岁以下患者中,66% 有私人保险;65 岁以上患者中,82% 享有 Medicare。多数患者(85%)来自本州,29% 来自低于全国贫困线地区,18% 来自非大都市地区。52%、40% 和 29% 患者到治疗中心的距离分别超过 30、60 和 120 英里。种族/族裔少数群体以及居住地距中心 >60 英里的患者,在使用商业产品或研究性产品方面没有显著差异。然而,来自非大都市地区及低于贫困线地区的患者较少接受商业产品治疗。中位随访 11 个月时,1 年总生存率(OS)为 63.2%(95% CI 59.9%–66.8%)。贫困与较低的 1 年 OS 相关(HR 0.4,95% CI 0.17–0.90,P = 0.031)。
本研究显示,CAR-T 治疗能够跨越社会人口学障碍提供,但也凸显考虑健康的社会决定因素对于优化所有患者的治疗可及性至关重要。
Chimeric antigen receptor T-cell (CAR-T) therapies are available for patients with Non-Hodgkin Lymphoma (NHL); however, their use has been limited in accessibility due to nondisease factors. PATIENTS &
We conducted a retrospective study evaluating the influence of sociodemographic factors on access and outcomes after CAR-T therapy for adult patients with B-cell NHL in our institution treated between 2016 and 2023.
Among 154 patients treated with CAR-T, 43% were older than 65 years, 68% male, and 14% non-White (including Hispanic). Of those under 65, 66% had private insurance, while 82% over 65 had Medicare. Most patients (85%) were from in-state, 29% from areas below the national poverty level and 18% from nonmetropolitan areas. Distance to the treatment center was greater than 30, 60 or 120 miles for 52%, 40% and 29% of patients, respectively. No significant differences were found in the use of commercial versus investigational products among racial/ethnic minorities or those living >60 miles from the center. However, patients from nonmetropolitan areas and those below the national poverty level were less likely to receive commercial products. With a median follow-up of 11 months, the 1-year overall survival (OS) was 63.2% (95 th CI 59.9%-66.8%). Poverty was associated with lower 1-year OS (HR 0.4, 95 th CI 0.17-0.90, P = .031).
Our study shows that CAR-T therapy can be delivered across sociodemographic barriers and underscores the importance of considering social determinants of health to optimize access for all patients.
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