FDA-approved therapies for chronic GVHD

被引:0
|
作者
Lee, Stephanie J. [1 ,2 ]
Zeiser, Robert [3 ]
机构
[1] Fred Hutchinson Canc Ctr, Clin Res Div, Seattle, WA USA
[2] Univ Washington, Dept Med, Seattle, WA USA
[3] Univ Freiburg, Fac Med, Med Ctr, Dept Med 1, Freiburg, Germany
基金
美国国家卫生研究院;
关键词
VERSUS-HOST-DISEASE; CONSENSUS DEVELOPMENT PROJECT; CLINICAL-TRIALS; CELL TRANSPLANTATION; IBRUTINIB; CRITERIA; RUXOLITINIB; PREVENTION; GLOBULIN; MURINE;
D O I
10.1182/blood.2024026633
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 approved by the US Food and Drug Administration (FDA) 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.
引用
收藏
页码:795 / 800
页数:6
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