Literature DB >> 25189727

Controversies and dilemmas in allogeneic transplantation for myelofibrosis.

Mohamed Shanavas1, Vikas Gupta2.   

Abstract

JAK1/2 inhibitors have broadened the therapeutic options in myelofibrosis. Though not curative, they result in a meaningful clinical benefit with relatively fewer side effects. In contrast, allogeneic hematopoietic cell transplantation (HCT) is a potentially curative option, but is associated with significant morbidity and mortality. Hence, an important question is the optimal timing of HCT in the era of JAK inhibitors. Timing of HCT is a crucial decision, and need to be individualized based on the personal preferences and goals of therapy; in addition to patient, disease, and transplant related factors. Risk stratification by the currently established prognostic scoring systems need to be further refined by incorporation of prognostically significant mutations to guide the treatment choices better. Data on use of JAK inhibitors prior to HCT have just started to emerge. We discuss some of the current controversies and dilemmas in transplantation for myelofibrosis based on a few real life scenarios. Crown
Copyright © 2014. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  CALR mutation; JAK inhibitors; allogeneic transplantation; leukemic transformation; myelofibrosis; prognosis

Mesh:

Substances:

Year:  2014        PMID: 25189727     DOI: 10.1016/j.beha.2014.07.007

Source DB:  PubMed          Journal:  Best Pract Res Clin Haematol        ISSN: 1521-6926            Impact factor:   3.020


  2 in total

1.  Impact of genomic alterations on outcomes in myelofibrosis patients undergoing JAK1/2 inhibitor therapy.

Authors:  Jay Y Spiegel; Caroline McNamara; James A Kennedy; Tony Panzarella; Andrea Arruda; Tracy Stockley; Mahadeo Sukhai; Mariam Thomas; Justyna Bartoszko; Jenny Ho; Nancy Siddiq; Dawn Maze; Aaron Schimmer; Andre Schuh; Hassan Sibai; Karen Yee; Jamie Claudio; Rebecca Devlin; Mark D Minden; Suzanne Kamel-Reid; Vikas Gupta
Journal:  Blood Adv       Date:  2017-09-08

2.  Limitations of fibrosis grade as diagnostic criteria for post polycythemia vera and essential thrombocytosis myelofibrosis.

Authors:  K Gowin; S Verstovsek; N Daver; N Pemmaraju; R Valdez; H Kosiorek; A Dueck; R Mesa
Journal:  Leuk Res       Date:  2015-04-17       Impact factor: 3.156

  2 in total

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