血液恶性肿瘤干细胞移植后移植物抗宿主病的预防和管理:欧洲血液和骨髓移植学会最新共识建议

Olaf Penack, Monia Marchetti, Mahmoud Aljurf, Mutlu Arat, Francesca Bonifazi, Rafael F Duarte, Sebastian Giebel, Hildegard Greinix, Mette D Hazenberg, Nicolaus Kröger, Stephan Mielke, Mohamad Mohty, Arnon Nagler, Jakob Passweg, Francesca Patriarca, Tapani Ruutu, Hélène Schoemans, Carlos Solano, Radovan Vrhovac, Daniel Wolff, Zinaida Peric
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引用次数: 0

摘要

移植物抗宿主疾病(GVHD)是异基因造血干细胞移植(HSCT)后导致死亡和发病的主要因素。在过去三年中,监管机构批准了一些新药,预防和治疗 GVHD 的临床方法也发生了很大变化。为了统一治疗方法,欧洲血液与骨髓移植学会(EBMT)更新了其临床实践建议。我们成立了一个由一名方法论专家和 22 名 GVHD 管理领域的专家组成的小组。选择专家的依据是他们在欧洲 GVHD 管理中的作用以及对该领域的贡献,如发表的论文、在会议上的发言以及其他研究。我们将 GRADE 流程应用于十个 PICO(患者、干预、比较者和结果)问题:专家组搜索证据,并对每个关键结果进行分级。在两次共识会议上,我们讨论了证据,并就建议的措辞和力度进行了投票。建议的主要更新包括(1)在类固醇难治性急性GVHD和类固醇难治性慢性GVHD中主要使用鲁索利替尼作为新的治疗标准;(2)在非亲缘供者的外周血干细胞移植中使用兔抗T细胞(胸腺细胞)球蛋白或移植后环磷酰胺作为标准的GVHD预防措施;(3)在类固醇难治性慢性GVHD的现有治疗方案中增加贝卢莫司地。EBMT 建议将这些建议作为异基因造血干细胞移植期间 GVHD 常规治疗的基础。目前的建议倾向于欧洲的做法,并不一定代表全球的偏好。
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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

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.

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