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美国造血干细胞移植与 CAR-T 细胞的可及性障碍

英文原题:Access barriers to hematopoietic stem cell transplantation and CAR T-cells in US.

查看英文原题

Access barriers to hematopoietic stem cell transplantation and CAR T-cells in US.

PubMed 2025/07/06(内容时间) Leuk Lymphoma Q3 · IF 2.1(JCR 2025)

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中文摘要

细胞疗法,包括造血干细胞移植(HCT)和嵌合抗原受体(CAR)T细胞疗法,已取得显著进展,导致适应症范围扩大和患者预后改善。尽管取得了这些进展,可及性仍然不公平,其驱动因素包括社会经济因素、医疗基础设施相关的差异以及产品本身的局限性。本综述概述了美国细胞疗法可及性的现状,重点关注识别障碍并探索潜在解决方案。其中许多障碍在全球范围内普遍存在,包括在低收入和中等收入国家,但未必在其他发达国家中有所体现,因为这些国家的医疗体系和资助模式不同。解决这些差异需要在多个层面采取行动,包括扩大基于社区的可及性、制造工艺创新、加强财政支持以及实施以公平为重点的举措。随着细胞疗法的不断发展,确保公平可及必须始终作为核心优先事项,以促进医学创新的包容性。

展开英文摘要原文

Cellular therapies, including hematopoietic stem cell transplantation (HCT) and chimeric antigen receptor (CAR) T-cell therapy, have undergone significant advancements, leading to broader indications and improved patient outcomes. Despite the progress, access remains inequitable, driven by disparities related to socioeconomic factors, healthcare infrastructure, and limitations associated with the products themselves. This review provides an overview of the current state of access to cellular therapies in the United States, with a focus on identifying barriers and exploring potential solutions.

Many of these barriers are shared globally, including in low- and middle-income countries, but are not necessarily mirrored in other developed nations, where healthcare systems and funding models differ.

Addressing these disparities will require action at many levels, including expanding community-based access, innovation in the manufacturing process, enhancing financial support, and implementing equity-focused initiatives. As cellular therapies continue to evolve, ensuring equitable access must remain a central priority to foster inclusiveness in medical innovation.

论文信息

作者
Odstrcil Bobillo MS、McClune B、Couriel DR
单位
Department of Medicine. Division of Hematology and Hematologic Malignancies, University of Utah Health Huntsman Cancer Institute, Salt Lake City, UT, USA.United States
文献类型
综述
期刊
Leukemia & lymphoma2025 Nov
原文标识
PubMed 40618383 · DOI 10.1080/10428194.2025.2513003