FDA-approved therapies for chronic GVHD
S
Stephanie J. Lee
R
Robert Zeiser
Abstract
Abstact 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.
Article Details
Journal
Blood
Volume / Issue
Vol. 145, Issue 8
Published
February 20, 2025
Pages
795-800
ISSN
0006-4971
Publisher
Elsevier BV
Authors (2)
S
Stephanie J. Lee
R
Robert Zeiser
Related Articles from this Journal
NOTCHing the MSC-endothelial interplay in the HSC niche
Simón Méndez-Ferrer
Aug 2026
10.1182/blood.2026034119
Procr+ endothelial progenitor cells govern hematopoiesis through fine-tuning mesenchymal stem cell niche signals
Chang Xu, Xue Lv et al.
Aug 2026
10.1182/blood.2025031474
Li C, Wu B, Li Y, et al. Loss of sphingosine kinase 2 promotes the expansion of hematopoietic stem cells by improving their metabolic fitness. <i>Blood</i> . 2022;140(15):1686-1701.
Aug 2026
10.1182/blood.2026035281
Haploidentical transplant, gene therapy, and standard care in sickle cell disease: a cost-effectiveness analysis
Karthik Chetlapalli, Satoko Ito et al.
Aug 2026
10.1182/blood.2025032290
Granulopoiesis under attack by mutant IDH1
Hideyo Hirai
Aug 2026
10.1182/blood.2026034486