Prophylaxis and management of graft-versus-host disease after stem-cell transplantation for haematological malignancies: updated consensus recommendations of the European Society for Blood and Marrow Transplantation
- PMID: 38184001
- DOI: 10.1016/S2352-3026(23)00342-3
Prophylaxis and management of graft-versus-host disease after stem-cell transplantation for haematological malignancies: updated consensus recommendations of the European Society for Blood and Marrow Transplantation
Abstract
Graft-versus-host disease (GVHD) is a major factor contributing to mortality and morbidity after allogeneic haematopoietic stem-cell transplantation (HSCT). In the last 3 years, there has been regulatory approval of new drugs and considerable change in clinical approaches to prophylaxis and management of GVHD. To standardise treatment approaches, the European Society for Blood and Marrow Transplantation (EBMT) has updated its clinical practice recommendations. We formed a panel of one methodologist and 22 experts in the field of GVHD management. The selection was made on the basis of their role in GVHD management in Europe and their contributions to the field, such as publications, presentations at conferences, and other research. We applied the GRADE process to ten PICO (patient, intervention, comparator, and outcome) questions: evidence was searched for by the panel and graded for each crucial outcome. In two consensus meetings, we discussed the evidence and voted on the wording and strengths of recommendations. Key updates to the recommendations include: (1) primary use of ruxolitinib in steroid-refractory acute GVHD and steroid-refractory chronic GVHD as the new standard of care, (2) use of rabbit anti-T-cell (thymocyte) globulin or post-transplantation cyclophosphamide as standard GVHD prophylaxis in peripheral blood stem-cell transplantations from unrelated donors, and (3) the addition of belumosudil to the available treatment options for steroid-refractory chronic GVHD. The EBMT proposes to use these recommendations as the basis for routine management of GVHD during allogenic HSCT. The current recommendations favour European practice and do not necessarily represent global preferences.
Copyright © 2024 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests OP received honoraria or travel support from Gilead, Jazz, Merck, Sharp & Dohme (MSD), Novartis, Pfizer, and Therakos; received research support from Incyte and Priothera; and is a member of advisory boards to Equillium Bio, Jazz, Gilead, Novartis, MSD, Omeros, Priothera, Sanofi, Shionogi, and SOBI. FP has received travel support and was member of advisory board of GlaxoSmithKline, Amgen, Roche, and Janssen. HG received honoraria for participation in advisory boards and speakers' bureau from Celgene, Gilead, Novartis, Roche, Sanofi, Takeda, and Therakos. HS reports having received personal fees from Incyte, Janssen, Novartis, Sanofi, and from the Belgian Hematological Society (BHS); reports research grants from Novartis and the BHS; and has received non-financial support (travel grants) from Gilead, Pfizer, the European Society for Blood and Marrow transplantation and the Center for International Bone Marrow Transplantation Research. MAr is on the advisory board of Neovii and reports research support from Therakos and Roche. NK received honoraria from Kite–Gilead, Jazz, MSD, Neovii Biotech, Novartis, Riemser, Pfizer, BMS; and research support from Neovii, Riemser, Novartis and Deutsche Knochenmarksperderdatei. AS has received honoraria from Takeda, Bristol-Myers Squibb–Celgene, MSD, Janssen, Amgen, Novartis, Kite–Gilead, Sanofi, Roche, and Alexion; is a consultant to Takeda, Bristol-Myers Squibb–Celgene, Novartis, Janssen, Gilead, Sanofi; and has received research support from Takeda. FB participated in advisory board meetings and received speaker fees from NEOVII, Sanofi, Takeda, and Novartis. SG received honoraria or travel support from Novartis and Janssen, and is member of advisory boards to Novartis and Janssen. ZP received honoraria from Sanofi and Therakos. DW received a research grant from Novartis, and received honoraria from Novartis, Takeda, Mallinckrodt, Sanofi, Incyte, Behring, and NEOVII.
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