依鲁替尼:循证评价其治疗晚期慢性淋巴细胞白血病的潜力。

Core Evidence Pub Date : 2013-01-01 Epub Date: 2013-05-16 DOI:10.2147/CE.S34068
Julio C Chavez, Eva Sahakian, Javier Pinilla-Ibarz
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引用次数: 22

摘要

慢性淋巴细胞白血病(CLL)是一种病程多变的异质性疾病,至今仍是一种不治之症。频繁复发和最终对氟达拉滨耐药是有症状的CLL的特征,预示着患者预后不佳。越来越多的证据表明,B细胞受体和NFkB等信号通路与CLL细胞的存活和增殖有关,最终与疾病的持续存在有关。布鲁顿酪氨酸激酶途径调节B细胞受体的下游激活,并已成为一个有吸引力的目标。依鲁替尼抑制布鲁顿酪氨酸激酶途径,从而诱导B细胞凋亡。在难治性/复发性CLL患者和老年treatment-naïve CLL患者中,I期和II期研究显示出令人印象深刻的反应率和出色的安全性。本文综述了依鲁替尼治疗慢性淋巴细胞白血病的临床前和临床数据。最近的研究显示伊鲁替尼、单克隆抗体和化学免疫治疗联合治疗的益处也进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ibrutinib: an evidence-based review of its potential in the treatment of advanced chronic lymphocytic leukemia.

Ibrutinib: an evidence-based review of its potential in the treatment of advanced chronic lymphocytic leukemia.

Chronic lymphocytic leukemia (CLL) is a heterogeneous disease with a variable course, and remains an incurable disease. Frequent relapses and eventual resistance to fludarabine characterize symptomatic CLL and portends a dismal prognosis for patients. Growing evidence has shown that signaling pathways such as the B cell receptor and NFkB are implicated in the survival and proliferation of the CLL cells which are ultimately associated with persistence of the disease. The Bruton's tyrosine kinase pathway regulates downstream activation of the B cell receptor and has emerged as an attractive target. Ibrutinib inhibits the Bruton's tyrosine kinase pathway, and consequently induces apoptosis of B cells. Phase I and II studies have shown impressive response rates with an excellent safety profile in patients with refractory/relapsed CLL and elderly treatment-naïve CLL patients. This paper reviews the preclinical and clinical data for ibrutinib when used in the treatment of CLL. Recent studies showing the benefit of combination therapy using ibrutinib, monoclonal antibodies, and chemoimmunotherapy are also discussed.

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Core Evidence
Core Evidence PHARMACOLOGY & PHARMACY-
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期刊介绍: Core Evidence evaluates the evidence underlying the potential place in therapy of drugs throughout their development lifecycle from preclinical to postlaunch. The focus of each review is to evaluate the case for a new drug or class in outcome terms in specific indications and patient groups The emerging evidence on new drugs is reviewed at key stages of development and evaluated against unmet needs
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