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移植物抗宿主病:以更低成本让老药新用。

Graft-versus-host disease: teaching old drugs new tricks at less cost.

机构信息

Stem Cell Transplant and Cellular Therapy, Henry Ford Health, Detroit, MI, United States.

Division of Hematology, Oncology, and Transplantation, University of Minnesota, Minneapolis, MN, United States.

出版信息

Front Immunol. 2023 Aug 3;14:1225748. doi: 10.3389/fimmu.2023.1225748. eCollection 2023.

Abstract

Graft-versus-host disease (GVHD) remains a major cause of morbidity and mortality after allogeneic stem cell transplantation (SCT). Currently, more patients can receive SCT. This is attributed to the use of reduced intensity regimens and the use of different GVHD prophylaxis that breaks the barrier of human leukocyte antigen, allowing an increase in the donor pool. Once an area with relatively few clinical trial options, there has been an increase in interest in GVHD prophylaxis and treatment, which has led to many US Food and Drug Administration (FDA) approvals. Although there is considerable excitement over novel therapies, many patients may not have access to them due to geographical or other resource constraints. In this review article, we summarize the latest evidence on how we can continue to repurpose drugs for GVHD prophylaxis and treatment. Drugs covered by our review include those that have been FDA approved for other uses for at least 15 years (since 2008); thus, they are likely to have generic equivalents available now or in the near future.

摘要

移植物抗宿主病(GVHD)仍然是异基因干细胞移植(SCT)后发病率和死亡率的主要原因。目前,更多的患者可以接受 SCT。这归因于使用强度降低的方案和使用不同的 GVHD 预防措施,这些措施打破了人类白细胞抗原的障碍,增加了供体库。曾经是临床试验选择相对较少的领域,现在对 GVHD 预防和治疗的兴趣增加,这导致了许多美国食品和药物管理局(FDA)的批准。尽管新型疗法令人兴奋,但由于地理或其他资源限制,许多患者可能无法获得这些疗法。在这篇综述文章中,我们总结了关于如何继续重新利用药物预防和治疗 GVHD 的最新证据。我们综述的药物包括那些自 2008 年以来至少已获得 FDA 批准用于其他用途 15 年以上的药物;因此,它们现在或不久的将来可能会有通用等效物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f988/10435076/12d218aa3ea2/fimmu-14-1225748-g001.jpg

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