成人费城染色体阳性急性淋巴细胞白血病的诊断和治疗。

International Journal of Hematologic Oncology Pub Date : 2016-09-01 Epub Date: 2016-09-23 DOI:10.2217/ijh-2016-0009
Xavier Thomas, Maël Heiblig
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引用次数: 0

摘要

随着酪氨酸激酶抑制剂(TKIs)的问世,费城染色体阳性(Ph+)急性淋巴细胞白血病(ALL)成人患者的治疗效果得到了大幅改善。目前,TKIs 已成为 Ph+ ALL 治疗不可或缺的组成部分。目前的共识是,与单纯化疗的历史对照患者相比,TKIs可改善患者的预后,并增加能够接受干细胞移植的患者人数。主要通过Abelson酪氨酸激酶突变诱导耐药性的新挑战已经出现。目前正在开发几种新型激酶抑制剂,它们具有更强的抗白血病活性。此外,招募或改造患者自身T细胞以对抗白血病细胞的新型免疫疗法也正在开发中,几年内可能会在Ph+ ALL治疗中占据重要地位。在本文中,我们回顾了成人 Ph+ ALL 的治疗方法,重点是 TKIs 和联合化疗方案。
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Diagnostic and treatment of adult Philadelphia chromosome-positive acute lymphoblastic leukemia.

The outcome of adult patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) has improved substantially with the introduction of tyrosine kinase inhibitors (TKIs). TKIs are now integral components of therapy for Ph+ ALL. The current consensus is that they improve patient outcomes compared with historical control patients treated with chemotherapy alone, and increase the number of patients able to receive stem cell transplant. New challenges have emerged with respect to induction of resistance mainly via Abelson tyrosine kinase mutations. Several novel kinase inhibitors with significantly more potent antileukemic activity are currently being developed. Furthermore novel immune therapies, which recruit or modify patient's own T cells to fight leukemic cells, are being developed and could find an important place in Ph+ ALL therapy by few years. In this article, we reviewed treatment approaches in adults with Ph+ ALL with a focus on TKIs and combined chemotherapy regimens.

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自引率
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发文量
3
审稿时长
13 weeks
期刊介绍: International Journal of Hematologic Oncology welcomes unsolicited article proposals. Email us today to discuss the suitability of your research and our options for authors, including Accelerated Publication. Find out more about publishing open access with us here.
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