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用于骨髓纤维化的Janus激酶抑制剂和异基因干细胞移植

Janus kinase inhibitors and allogeneic stem cell transplantation for myelofibrosis.

作者信息

Gupta Vikas, Gotlib Jason, Radich Jerald P, Kröger Nicolaus M, Rondelli Damiano, Verstovsek Srdan, Deeg H Joachim

机构信息

Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

Stanford University School of Medicine, Palo Alto, California.

出版信息

Biol Blood Marrow Transplant. 2014 Sep;20(9):1274-81. doi: 10.1016/j.bbmt.2014.03.017. Epub 2014 Mar 27.

Abstract

Myelofibrosis (MF) is a manifestation of several disorders of hematopoiesis, collectively referred to as myeloproliferative neoplasms. Allogeneic hematopoietic stem cell transplantation (ASCT) is the only therapy with proven curative potential. However, most patients with MF are in their 6th or 7th decade of life, and only some of these patients have been considered suitable transplantation candidates. The development of reduced-intensity conditioning regimens with limited toxicity has allowed clinicians to offer ASCT to a growing number of older patients. The availability of Janus Kinase (JAK) 1/2 inhibitors allows clinicians to provide symptom relief and improved quality of life for MF patients. These drugs may also affect the decision regarding, in particular, the timing of ASCT. Future studies need to address the role of JAK1/2 inhibitors in patients who are transplantation candidates and determine their role before and, possibly, after transplantation. The identification of indications for the use of JAK1/2 inhibitors in the context of transplantation may lead to new therapeutic strategies for patients with MF.

摘要

骨髓纤维化(MF)是几种造血系统疾病的一种表现,统称为骨髓增殖性肿瘤。异基因造血干细胞移植(ASCT)是唯一具有经证实的治愈潜力的疗法。然而,大多数MF患者处于60或70岁年龄段,且只有其中一些患者被认为是合适的移植候选者。毒性有限的减低强度预处理方案的发展使临床医生能够为越来越多的老年患者提供ASCT。Janus激酶(JAK)1/2抑制剂的出现使临床医生能够为MF患者缓解症状并改善生活质量。这些药物也可能会影响特别是关于ASCT时机的决策。未来的研究需要探讨JAK1/2抑制剂在移植候选患者中的作用,并确定其在移植前以及可能在移植后的作用。确定在移植背景下使用JAK1/2抑制剂的指征可能会为MF患者带来新的治疗策略。

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