FDA-approved therapies for chronic GVHD

IF 23.1 1区 医学 Q1 HEMATOLOGY Blood Pub Date : 2025-01-02 DOI:10.1182/blood.2024026633
Stephanie J. Lee, Robert Zeiser
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Abstract

Despite novel prophylactic regimens, chronic graft-versus-host disease (cGVHD) remains a challenging complication after allogeneic hematopoietic cell transplantation. cGVHD can affect multiple organs and reduces quality of life, and treatment can cause serious adverse effects. In the past 10 years, the drugs ibrutinib, ruxolitinib, belumosudil, and axatilimab were US Food and Drug Administration (FDA) approved for cGVHD. Here, we discuss which signaling pathways and cell types are targeted, the clinical studies that were the basis for FDA approval, and future directions for clinical research.
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fda批准的慢性GVHD疗法
尽管有新的预防方案,慢性移植物抗宿主病(cGVHD)仍然是异基因造血细胞移植后的一个具有挑战性的并发症。cGVHD可影响多个器官,降低生活质量,治疗可引起严重的不良反应。在过去的10年里,伊鲁替尼、鲁索利替尼、白莫沙地尔和阿替利单抗等药物被美国食品和药物管理局(FDA)批准用于治疗cGVHD。在这里,我们讨论了哪些信号通路和细胞类型是靶向的,作为FDA批准基础的临床研究,以及临床研究的未来方向。
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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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