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伊布替尼:对其治疗晚期慢性淋巴细胞白血病潜力的循证综述

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

作者信息

Chavez Julio C, Sahakian Eva, Pinilla-Ibarz Javier

机构信息

H Lee Moffitt Cancer and Research Institute, Division of Malignant Hematology, and University of South Florida, Tampa, FL, USA.

出版信息

Core Evid. 2013;8:37-45. doi: 10.2147/CE.S34068. Epub 2013 May 16.

Abstract

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.

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,目前仍是无法治愈的疾病。症状性CLL的特征是频繁复发并最终对氟达拉滨产生耐药性,这预示着患者的预后不佳。越来越多的证据表明,诸如B细胞受体和NFkB等信号通路与CLL细胞的存活和增殖有关,而这最终与疾病的持续存在相关。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靶点。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。I期和II期研究表明,难治性/复发性CLL患者以及未经治疗的老年CLL患者使用依鲁替尼后反应率令人印象深刻,且安全性良好。本文综述了依鲁替尼用于治疗CLL的临床前和临床数据。还讨论了近期显示依鲁替尼联合单克隆抗体和化学免疫疗法治疗益处的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9564/3662532/eb5dab3ccc84/ce-8-037f1.jpg

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