How we manage JAK inhibition in allogeneic transplantation for myelofibrosis
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How we manage JAK inhibition in allogeneic transplantation for myelofibrosis. / Ballinger, Tarah J; Savani, Bipin N; Gupta, Vikas; Kröger, Nicolaus-Martin; Mohty, Mohamad.
In: EUR J HAEMATOL, Vol. 94, No. 2, 02.2015, p. 115-119.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - How we manage JAK inhibition in allogeneic transplantation for myelofibrosis
AU - Ballinger, Tarah J
AU - Savani, Bipin N
AU - Gupta, Vikas
AU - Kröger, Nicolaus-Martin
AU - Mohty, Mohamad
N1 - This article is protected by copyright. All rights reserved.
PY - 2015/2
Y1 - 2015/2
N2 - Hematopoietic stem cell transplantation (HCT) is currently the only curative treatment for myelofibrosis (MF), but this option is complicated by high incidences of associated morbidity and mortality. Ruxolitinib, a Janus activated kinase (JAK) 1/2 inhibitor, has proven to be beneficial in reduction of splenomegaly, improvement of constitutional symptoms, and possibly in overall survival. However, use of JAK inhibitors in the peri-transplant period has been complicated by unpredictable response, return of MF symptoms or cytokine storm reaction upon discontinuation, and lack of long term response data. This review considers the current limited available data on JAK inhibitor use prior to HCT, including common side effects and possible impact of severe adverse events on discontinuation of the drug. We provide our experience and recommendations regarding use of JAK inhibition in patients undergoing HCT. Additional studies are needed to determine the optimal schedule of JAK inhibitors in the transplant protocols and their impact on engraftment, graft versus host disease, and survival. This article is protected by copyright. All rights reserved.
AB - Hematopoietic stem cell transplantation (HCT) is currently the only curative treatment for myelofibrosis (MF), but this option is complicated by high incidences of associated morbidity and mortality. Ruxolitinib, a Janus activated kinase (JAK) 1/2 inhibitor, has proven to be beneficial in reduction of splenomegaly, improvement of constitutional symptoms, and possibly in overall survival. However, use of JAK inhibitors in the peri-transplant period has been complicated by unpredictable response, return of MF symptoms or cytokine storm reaction upon discontinuation, and lack of long term response data. This review considers the current limited available data on JAK inhibitor use prior to HCT, including common side effects and possible impact of severe adverse events on discontinuation of the drug. We provide our experience and recommendations regarding use of JAK inhibition in patients undergoing HCT. Additional studies are needed to determine the optimal schedule of JAK inhibitors in the transplant protocols and their impact on engraftment, graft versus host disease, and survival. This article is protected by copyright. All rights reserved.
U2 - 10.1111/ejh.12455
DO - 10.1111/ejh.12455
M3 - SCORING: Journal article
C2 - 25256963
VL - 94
SP - 115
EP - 119
JO - EUR J HAEMATOL
JF - EUR J HAEMATOL
SN - 0902-4441
IS - 2
ER -