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慢性髓系白血病认识的最新进展:我们目前的状况如何?

Recent advances in understanding chronic myeloid leukemia: where do we stand?

作者信息

Kumar Rahul, Krause Daniela S

机构信息

Georg-Speyer-Haus, Institute for Tumor Biology and Experimental Therapy, 60596 Frankfurt, Germany.

German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Fac Rev. 2021 Apr 1;10:35. doi: 10.12703/r/10-35. eCollection 2021.

Abstract

While the need for complete eradication of leukemic stem cells (LSCs) in chronic myeloid leukemia may be controversial, it is agreed that remaining LSCs are the cause of relapse and disease progression. Current efforts are focused on the understanding of the persistence of immunophenotypically defined LSCs, which feature abnormalities in signaling pathways relating to autophagy, metabolism, epigenetics, and others and are influenced by leukemia cell-extrinsic factors such as the immune and bone marrow microenvironments. In sum, these elements modulate response and resistance to therapies and the clinical condition of treatment-free remission (TFR), the newly established goal in CML treatment, once the patient has achieved a durable molecular remission after treatment with tyrosine kinase inhibitors. Novel combination therapies based on these identified vulnerabilities of LSCs, aimed at the induction or maintenance of TFR, are being developed, while other research is directed at the elucidation of factors mediating progression to blast crisis.

摘要

虽然在慢性髓性白血病中彻底清除白血病干细胞(LSCs)的必要性可能存在争议,但人们一致认为,残留的LSCs是复发和疾病进展的原因。目前的研究重点是了解免疫表型定义的LSCs的持久性,这些LSCs在与自噬、代谢、表观遗传学等相关的信号通路中存在异常,并受到白血病细胞外在因素的影响,如免疫和骨髓微环境。总之,这些因素调节对治疗的反应和耐药性以及无治疗缓解(TFR)的临床状况,TFR是慢性髓性白血病治疗的新确立目标,一旦患者在接受酪氨酸激酶抑制剂治疗后实现持久的分子缓解。基于这些已确定的LSCs弱点的新型联合疗法正在开发中,旨在诱导或维持TFR,而其他研究则致力于阐明介导疾病进展为急变期的因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e2a/8103906/f4caa6b0364a/facrev-10-35-g001.jpg

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