Chronic Myeloid Leukemia, from Pathophysiology to Treatment-Free Remission: A Narrative Literature Review.

IF 2.1 Q3 HEMATOLOGY
Ikhwan Rinaldi, Kevin Winston
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引用次数: 5

Abstract

Chronic myeloid leukemia (CML) is one of the most common leukemias occurring in the adult population. The course of CML is divided into three phases: the chronic phase, the acceleration phase, and the blast phase. Pathophysiology of CML revolves around Philadelphia chromosome that constitutively activate tyrosine kinase through BCR-ABL1 oncoprotein. In the era of tyrosine kinase inhibitors (TKIs), CML patients now have a similar life expectancy to people without CML, and it is now very rare for CML patients to progress to the blast phase. Only a small proportion of CML patients have resistance to TKI, caused by BCR-ABL1 point mutations. CML patients with TKI resistance should be treated with second or third generation TKI, depending on the BCR-ABL1 mutation. Recently, many studies have shown that it is possible for CML patients who achieve a long-term deep molecular response to stop TKIs treatment and maintain remission. This review aimed to provide an overview of CML, including its pathophysiology, clinical manifestations, the role of stem cells, CML treatments, and treatment-free remission.

Abstract Image

Abstract Image

慢性髓性白血病,从病理生理到无治疗缓解:一篇叙述性文献综述。
慢性髓性白血病(CML)是发生在成人人群中最常见的白血病之一。慢性粒细胞白血病的病程可分为三个阶段:慢性期、加速期和爆炸期。CML的病理生理机制围绕费城染色体,该染色体通过BCR-ABL1癌蛋白组成性地激活酪氨酸激酶。在酪氨酸激酶抑制剂(TKIs)的时代,CML患者的预期寿命现在与没有CML的人相似,现在CML患者进展到blast期的情况非常罕见。由于BCR-ABL1点突变,只有一小部分CML患者对TKI有耐药性。根据BCR-ABL1突变,对TKI耐药的CML患者应接受第二代或第三代TKI治疗。最近,许多研究表明,实现长期深层分子反应的CML患者有可能停止TKIs治疗并维持缓解。本文综述了慢性粒细胞白血病的病理生理、临床表现、干细胞的作用、治疗方法和无治疗缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
94
审稿时长
16 weeks
期刊介绍: The Journal of Blood Medicine is an international, peer-reviewed, open access, online journal publishing laboratory, experimental and clinical aspects of all topics pertaining to blood based medicine including but not limited to: Transfusion Medicine (blood components, stem cell transplantation, apheresis, gene based therapeutics), Blood collection, Donor issues, Transmittable diseases, and Blood banking logistics, Immunohematology, Artificial and alternative blood based therapeutics, Hematology including disorders/pathology related to leukocytes/immunology, red cells, platelets and hemostasis, Biotechnology/nanotechnology of blood related medicine, Legal aspects of blood medicine, Historical perspectives. Original research, short reports, reviews, case reports and commentaries are invited.
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