酪氨酸激酶抑制剂时代慢性髓系白血病的异基因造血干细胞移植

Ahmet Emre Emre Eskazan, M. Tiribelli
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引用次数: 2

摘要

酪氨酸激酶抑制剂(TKI)的引入极大地改善了慢性髓性白血病(CML)患者的预后,因此改变了这种疾病的治疗方案。在第一个TKI伊马替尼出现之前,同种异体造血干细胞移植(alloSCT)是治疗CML的唯一方法,所有符合移植条件的患者都被推荐到移植中心进行移植。如今,随着五种不同TKI的广泛应用,同种异体移植的适应症已经减少到仅包括晚期CML患者和多次TKI治疗失败的患者。尽管如此,即使在TKI时代,同种异体细胞移植仍保持其治疗潜力。在此,作者概述了同种异体移植治疗CML的适应症以及移植前后TKI的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allogeneic Haematopoietic Stem Cell Transplantation for Chronic Myeloid Leukaemia in the Era of Tyrosine Kinase Inhibitors
The introduction of tyrosine kinase inhibitors (TKI) has dramatically improved the prognosis of chronic myeloid leukaemia (CML) patients and, therefore, changed the therapeutic scenario of this disease. Before the advent of the first TKI imatinib, allogeneic haematopoietic stem cell transplantation (alloSCT) was the only curative approach for CML, and all patients deemed eligible for transplant were referred to a centre for transplant where possible. Nowadays, with the wide availability of five different TKI, indications to alloSCT have been reduced to only include patients in the advanced phase of CML and those with multiple TKI treatment failures. Nonetheless, even in the TKI era, alloSCT retains its curative potential. Herein, the authors give an overview of the indications to allogeneic transplant for CML and the management of TKI in the pre and post-transplant settings.
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