Daenen L G M, van der Wagen L E, Bonneville E F, López-Corral L, Bukauskas A, Bornhäuser M, Beguin Y, Itäla-Remes M, Hoogenboom J D, de Wreede L C, Malard F, Chabannon C, Dazzi F, Ruggeri A, Kuball J
Department of Hematology, University Medical Centre Utrecht, Utrecht, The Netherlands.
EBMT Study Unit, Leiden, The Netherlands.
Bone Marrow Transplant. 2025 May;60(5):708-714. doi: 10.1038/s41409-025-02531-3. Epub 2025 Feb 20.
Acute graft-versus-host disease (aGvHD) remains a significant complication of allogeneic hematopoietic cell transplantation, with 40% of patients failing to respond to high-dose steroids. Ruxolitinib has become the standard treatment for steroid-refractory aGvHD (SR-GvHD), but its failure in approximately one-third of cases highlights the need for alternative therapies. Mesenchymal stromal cells (MSCs), known for their immunomodulatory properties, are suggested as a treatment option, but their role in SR-GvHD remains unclear. To better understand MSC therapy outcomes, the EBMT Cellular Therapy & Immunobiology Working Party conducted a survey of centers treating >20 SR-GvHD patients with MSCs between 2007 and 2020. Data from 313 patients were analyzed, revealing a 44.5% overall response rate at day 28. Responders at day 7 had a higher likelihood of maintaining responses by day 28. Using a landmark analysis, the overall survival at 12 months, conditional on being alive at day 28, was 39.2%. Survival at 12 months was 48.6% for responders, compared to 24.4% for non-responders. Despite manufacturing variabilities, MSCs produced by academic pharma appear effective in SR-GvHD, offering a viable treatment alternative for heavily pretreated patients. These findings support further investigation of MSCs to establish standardized protocols and validate their efficacy as third-line therapy for SR-GvHD.
急性移植物抗宿主病(aGvHD)仍然是异基因造血细胞移植的一个重要并发症,40%的患者对大剂量类固醇无反应。鲁索替尼已成为类固醇难治性aGvHD(SR-GvHD)的标准治疗方法,但其在约三分之一的病例中失败凸显了对替代疗法的需求。间充质基质细胞(MSC)以其免疫调节特性而闻名,被建议作为一种治疗选择,但其在SR-GvHD中的作用仍不清楚。为了更好地了解MSC治疗的结果,欧洲血液与骨髓移植协会(EBMT)细胞治疗与免疫生物学工作组对2007年至2020年间用MSC治疗20例以上SR-GvHD患者的中心进行了一项调查。分析了313例患者的数据,结果显示在第28天的总体缓解率为44.5%。在第7天有反应的患者在第28天维持反应的可能性更高。采用里程碑分析,以第28天存活为条件,12个月时的总生存率为39.2%。有反应者12个月时的生存率为48.6%,无反应者为24.4%。尽管存在生产差异,但学术制药公司生产的MSC在SR-GvHD中似乎有效,为经过大量预处理的患者提供了一种可行的治疗选择。这些发现支持对MSC进行进一步研究,以建立标准化方案并验证其作为SR-GvHD三线治疗的疗效。