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:CAR-T for all? Barriers, facilitators, and interventions to commercial CAR T-cell therapy access.
CAR-T for all? Barriers, facilitators, and interventions to commercial CAR T-cell therapy access.
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CAR-T 细胞免疫治疗已彻底改变了血液系统恶性肿瘤的治疗,尤其是在B细胞急性淋巴细胞白血病、B细胞非霍奇金淋巴瘤和多发性骨髓瘤中。然而,在种族和族裔少数群体中,已证实CAR-T 细胞免疫治疗的可及性不公平。本范围综述审查了37篇已发表文献,内容涉及获取商业化CAR-T 疗法的障碍和促进因素,以及减轻可及性不公平的干预措施。结果使用社会生态模型在患者、提供者、机构和政策层面进行组织,并强调这些障碍和促进因素如何对种族和族裔少数群体造成不成比例的影响。障碍复杂,存在于所有社会生态层面,并且仅识别出两项针对少数群体获取CAR-T 疗法差异的已发表干预措施。讨论了关键研究空白,包括由客观一手数据支持的障碍数量有限,以及缺乏由患者识别出的障碍。总体而言,本范围综述中识别出的障碍、促进因素和干预措施可为全面的多层次策略提供信息,以消除商业化CAR-T 细胞免疫治疗的可及性不公平。
Chimeric antigen receptor T-cell (CAR-T) immunotherapy has revolutionized the treatment of hematologic malignancies, especially in B-cell acute lymphoblastic leukemia, B-cell non-Hodgkin lymphoma, and multiple myeloma.
However, inequitable access to CAR T-cell immunotherapy has been demonstrated among racial and ethnic minority populations. This scoping review examined 37 works of published literature on barriers and facilitators to accessing commercial CAR-T therapy, as well as interventions to mitigate access inequities. The results are organized using the socio-ecological model across patient, provider, institutional, and policy levels, and highlight how these barriers and facilitators can disproportionately affect racial and ethnic minority populations.
Barriers are complex and present at all socio-ecological levels, and only two published interventions that target minority access disparities to CAR-T therapy were identified. Key research gaps, including the limited number of barriers supported by objective, primary data and the absence of patient-identified barriers, are discussed. Collectively, the barriers, facilitators, and interventions identified in this scoping review can inform comprehensive, multilevel strategies to eliminate access inequities to commercial CAR T-cell immunotherapy.
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