Lee Stephanie J, Zeiser Robert
Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Department of Medicine, University of Washington, Seattle, WA.
Blood. 2025 Feb 20;145(8):795-800. doi: 10.1182/blood.2024026633.
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.
尽管有新的预防性治疗方案,但慢性移植物抗宿主病(cGVHD)仍然是异基因造血细胞移植后具有挑战性的并发症。cGVHD可累及多个器官并降低生活质量,且治疗会导致严重不良反应。在过去10年中,伊布替尼、芦可替尼、贝利司他和阿沙替尼单抗已获美国食品药品监督管理局(FDA)批准用于治疗cGVHD。在此,我们讨论这些药物所靶向的信号通路和细胞类型、作为FDA批准依据的临床研究以及临床研究的未来方向。