The use of MSCs in steroid-refractory acute GvHD in Europe: a survey from the EBMT cellular therapy & immunobiology working party

被引:0
作者
Daenen, L. G. M. [1 ]
van der Wagen, L. E. [1 ]
Bonneville, E. F. [2 ,3 ]
Lopez-Corral, L. [4 ]
Bukauskas, A. [5 ]
Bornhaeuser, M. [6 ]
Beguin, Y. [7 ,8 ]
Itaela-Remes, M. [9 ]
Hoogenboom, J. D. [2 ]
de Wreede, L. C. [3 ]
Malard, F. [10 ]
Chabannon, C. [11 ,12 ]
Dazzi, F. [13 ]
Ruggeri, A. [14 ]
Kuball, J. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Hematol, Utrecht, Netherlands
[2] EBMT Study Unit, Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Biomed Data Sci, Leiden, Netherlands
[4] Hosp Univ Salamanca Spain, CIBERONC Ctr Invest Canc IBMCC USAL CSIC, Hematol Dept, IBSAL, Salamanca, Spain
[5] Vilnius Univ Hosp Santaros Klin, Vilnius, Lithuania
[6] Tech Univ Dresden, Univ Hosp Dresden, Dresden, Germany
[7] CHU Liege, Liege, Belgium
[8] Univ Liege, Liege, Belgium
[9] Turku Univ Hosp, Turku, Finland
[10] Sorbonne Univ, AP HP, Hop St Antoine,Ctr Rech St Antoine CRSA,INSERM, Serv dHematol Clin & Therapie Cellulaire, Paris, France
[11] Univ Aix Marseille, Inst Paoli Calmettes, Ctr Lutte Canc, Inserm,CBT, Marseille, France
[12] Univ Aix Marseille, Ctr Invest Clin Biotherapies, Inserm, CBT 1409, Marseille, France
[13] Kings Coll London, Comprehens Canc Ctr, London, England
[14] IRCCS San Raffaele Sci Inst, Hematol & Bone Marrow Transplantat Unit, Milan, Italy
关键词
MESENCHYMAL STEM-CELLS; VERSUS-HOST-DISEASE; STROMAL CELLS; RESISTANT; INFUSION;
D O I
10.1038/s41409-025-02531-3
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
收藏
页码:708 / 714
页数:7
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