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Cholesterol esterification inhibition and imatinib treatment synergistically inhibit growth of BCR-ABL mutation-independent resistant chronic myelogenous leukemia.胆固醇酯化抑制与伊马替尼治疗协同抑制BCR-ABL突变非依赖性耐药慢性粒细胞白血病的生长。
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本文引用的文献

1
Bosutinib safety and management of toxicity in leukemia patients with resistance or intolerance to imatinib and other tyrosine kinase inhibitors.博舒替尼治疗对伊马替尼和其他酪氨酸激酶抑制剂耐药或不耐受的白血病患者的安全性和毒性管理。
Blood. 2014 Feb 27;123(9):1309-18. doi: 10.1182/blood-2013-07-513937. Epub 2013 Dec 17.
2
Ponatinib in refractory Philadelphia chromosome-positive leukemias.波纳替尼治疗难治性费城染色体阳性白血病。
N Engl J Med. 2012 Nov 29;367(22):2075-88. doi: 10.1056/NEJMoa1205127.
3
Phase 2 study of subcutaneous omacetaxine mepesuccinate after TKI failure in patients with chronic-phase CML with T315I mutation.T315I 突变的慢性期 CML 患者 TKI 治疗失败后皮下注射奥马曲星的 2 期研究。
Blood. 2012 Sep 27;120(13):2573-80. doi: 10.1182/blood-2012-03-415307. Epub 2012 Aug 15.
4
Predictive value of early molecular response in patients with chronic myeloid leukemia treated with first-line dasatinib.一线达沙替尼治疗慢性髓性白血病患者早期分子反应的预测价值。
Blood. 2012 Jul 12;120(2):291-4. doi: 10.1182/blood-2012-01-407486. Epub 2012 May 29.
5
Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML).慢性髓性白血病(CML)中早期的分子和细胞遗传学应答可预测长期无进展生存和总生存。
Leukemia. 2012 Sep;26(9):2096-102. doi: 10.1038/leu.2012.85. Epub 2012 Mar 26.
6
Bosutinib is active in chronic phase chronic myeloid leukemia after imatinib and dasatinib and/or nilotinib therapy failure.博舒替尼对于伊马替尼、达沙替尼和/或尼洛替尼治疗失败后的慢性期慢性髓性白血病具有活性。
Blood. 2012 Apr 12;119(15):3403-12. doi: 10.1182/blood-2011-11-390120. Epub 2012 Feb 27.
7
Chronic myeloid leukemia: clinical impact of BCR-ABL1 mutations and other lesions associated with disease progression.慢性髓细胞白血病:BCR-ABL1 突变及其他与疾病进展相关的病变的临床影响。
Semin Oncol. 2012 Feb;39(1):58-66. doi: 10.1053/j.seminoncol.2011.11.002.
8
Successful treatment of a chronic-phase T-315I-mutated chronic myelogenous leukemia patient with a combination of imatinib and interferon-alfa.伊马替尼联合干扰素-α成功治疗慢性期 T315I 突变慢性髓性白血病患者。
Int J Hematol. 2012 Feb;95(2):209-13. doi: 10.1007/s12185-012-1005-1. Epub 2012 Jan 20.
9
BCR-ABL1 kinase domain mutations: methodology and clinical evaluation.BCR-ABL1 激酶结构域突变:方法学与临床评估。
Am J Hematol. 2012 Mar;87(3):298-304. doi: 10.1002/ajh.22272. Epub 2012 Jan 9.
10
Undetectable molecular residual disease after omacetaxine and nilotinib combination therapy in an imatinib-resistant chronic myeloid leukaemia patient harbouring the BCR-ABL1 T315I gatekeeper mutation.在一名携带BCR-ABL1 T315I守门基因突变的伊马替尼耐药慢性髓性白血病患者中,奥马西他辛与尼罗替尼联合治疗后分子残留病检测不到。
Br J Haematol. 2012 May;157(3):407-10. doi: 10.1111/j.1365-2141.2011.09016.x. Epub 2012 Jan 9.

慢性髓性白血病酪氨酸激酶抑制剂治疗耐药:临床观点与新兴治疗选择。

Resistance to tyrosine kinase inhibition therapy for chronic myelogenous leukemia: a clinical perspective and emerging treatment options.

机构信息

The University of Texas, MD Anderson Cancer Center, Houston, TX.

出版信息

Clin Lymphoma Myeloma Leuk. 2013 Oct;13(5):515-29. doi: 10.1016/j.clml.2013.03.018. Epub 2013 Jul 26.

DOI:10.1016/j.clml.2013.03.018
PMID:23890944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4160831/
Abstract

The development of tyrosine kinase inhibitors (TKIs) has led to extended lifespans for many patients with chronic myelogenous leukemia (CML). However, 20% to 30% of patients fail to respond, respond suboptimally, or experience disease relapse after treatment with imatinib. A key factor is drug resistance. The molecular mechanisms implicated in this resistance include those that involve upregulation or mutation of BCR-ABL kinase and those that are BCR-ABL independent. The clinical consequences of these molecular mechanisms of resistance for disease pathogenesis remain open for debate. This review summarizes the molecular mechanisms and clinical consequences of TKI resistance and addresses the current and future treatment approaches for patients with TKI-resistant CML.

摘要

酪氨酸激酶抑制剂(TKIs)的发展使许多慢性髓性白血病(CML)患者的寿命得以延长。然而,仍有 20%至 30%的患者对伊马替尼治疗无反应、反应不佳或出现疾病复发。一个关键因素是药物耐药性。涉及 BCR-ABL 激酶上调或突变以及 BCR-ABL 不依赖的耐药机制与这种耐药性有关。这些耐药分子机制对疾病发病机制的临床后果仍存在争议。本文综述了 TKI 耐药的分子机制和临床后果,并探讨了 TKI 耐药 CML 患者目前和未来的治疗方法。