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维奈托克:抑制Bcl-2用于治疗慢性淋巴细胞白血病。

Venetoclax: Bcl-2 inhibition for the treatment of chronic lymphocytic leukemia.

作者信息

Del Poeta G, Postorino M, Pupo L, Del Principe M I, Dal Bo M, Bittolo T, Buccisano F, Mariotti B, Iannella E, Maurillo L, Venditti A, Gattei V, de Fabritiis P, Cantonetti M, Amadori S

机构信息

Hematology, Dipartimento di Biomedicina e Prevenzione, Universit à degli Studi di Roma Tor Vergata, Rome, Italy.

Clinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano (PN), Italy.

出版信息

Drugs Today (Barc). 2016 Apr;52(4):249-60. doi: 10.1358/dot.2016.52.4.2470954.

Abstract

Venetoclax (ABT-199) is a small-molecule selective oral inhibitor of the antiapoptotic protein Bcl-2 that promotes programmed cell death of chronic lymphocytic leukemia (CLL) cells regulating the release of proapoptotic factors, such as Smac/Diablo, apoptosis-inducing factor (AIF) and cytochrome c. In April 2016, the U.S. Food and Drug Administration (FDA) granted accelerated approval to venetoclax for patients diagnosed with CLL with 17p deletion, as detected by an FDA-approved test, who have received at least one prior therapy. This review will focus on the mechanism of action, preclinical studies and clinical development of venetoclax both as a monotherapy and in combination with other drugs for CLL in the current milieu of therapy dominated by novel tyrosine kinase inhibitors such as ibrutinib and idelalisib.

摘要

维奈托克(ABT-199)是一种抗凋亡蛋白Bcl-2的小分子选择性口服抑制剂,可促进慢性淋巴细胞白血病(CLL)细胞的程序性细胞死亡,调节促凋亡因子的释放,如Smac/ Diablo、凋亡诱导因子(AIF)和细胞色素c。2016年4月,美国食品药品监督管理局(FDA)加速批准维奈托克用于经FDA批准的检测方法检测出存在17p缺失、且至少接受过一种先前治疗的CLL患者。在当前以伊布替尼和idelalisib等新型酪氨酸激酶抑制剂为主导的治疗环境中,本综述将重点关注维奈托克作为单药疗法以及与其他药物联合用于CLL的作用机制、临床前研究和临床开发情况。

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