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Allogeneic stem-cell transplantation for myelofibrosis

Lavi, Noaa; Rowe, Jacob M.a,b,c; Zuckerman, Tsilaa,c

doi: 10.1097/MOH.0000000000000381

Purpose of review Allogeneic hematopoietic stem-cell transplantation (HSCT) remains the only curative therapy for myelofibrosis. The number of HSCTs performed for this indication has been steadily increasing over the past years, even after the approval of the Janus kinase (JAK) inhibitor, ruxolitinib. This increase may be attributed to improved patient selection based on new prognostic molecular markers, more frequent use of matched unrelated donors, secondary to better (high-resolution) human leukocyte antigen typing and supportive care. Ruxolitinib approval raises new questions regarding the role of JAK inhibitors in the transplant setting.

Recent findings The current review summarizes recent updates on HSCT in myelofibrosis. Predictors for transplant outcomes, and specific considerations related to myelofibrosis patient selection for HSCT (e.g. molecular risk stratification) are reviewed. In addition, this review will consider management of myelofibrosis patients in the peritransplant period, including the role of ruxolitinib in the pretransplant period, pre and posttransplant splenomegaly, transplant protocols, posttransplant follow-up of minimal residual disease and interventions in the event of poor engraftment.

Summary HSCT remains a highly relevant treatment option for myelofibrosis in the era of JAK inhibitors. Recent advances may contribute to a refined definition of HSCT eligibility and identification of the optimal transplantation time, conditioning protocols and posttransplant management.

aDepartment of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa

bDepartment of Hematology, Shaare Zedek Medical Center, Jerusalem

cRuth and Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel

Correspondence to Jacob M. Rowe, MD, Department of Hematology, Shaare Zedek Medical Center, 12, Shmu’el Bait St, Jerusalem 9103102, Israel. Tel: +972 2 6555204; fax: +972 2 6555755; e-mail:

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