克服伊鲁替尼耐药性的研究进展。

IF 1.8 4区 医学 Q2 Medicine
Xiang-Yu Ma, Min Zhao, Yi-Dong Li, Yanglu Chen, Liuya Wei, Zhe-Sheng Chen
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引用次数: 0

摘要

Ibrutinib是一种口服小分子靶向药物,是全球首个获批上市的布鲁顿酪氨酸激酶(BTK)抑制剂。它通过调节细胞增殖、凋亡和迁移起作用,已被证明对b细胞淋巴瘤(包括慢性淋巴细胞白血病或小淋巴细胞淋巴瘤和套细胞淋巴瘤)具有较高的疗效和良好的安全性。但部分患者不可避免地出现耐药性和疾病复发,导致预后较差。本文对伊鲁替尼耐药抑制剂的相关文献进行综述,供临床参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research progress in overcoming ibrutinib drug resistance.

Ibrutinib, an oral small-molecule targeted drug, has been the first Bruton tyrosine kinase (BTK) inhibitor in the world to be approved for the market. It works by regulating cell proliferation, apoptosis and migration, and has been proven to exhibit high efficacy and good safety in the treatment of B-cell lymphomas, including chronic lymphocytic leukemia or small lymphocytic lymphoma and mantle cell lymphoma. However, some patients inevitably have drug resistance and disease recurrence, resulting in a poor prognosis. This article serves as a clinical reference by summarizing the related literature on ibrutinib resistance inhibitors.

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来源期刊
Drugs of today
Drugs of today 医学-药学
CiteScore
3.90
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: An international, peer-reviewed journal publishing monographs on new products entering the market and review articles. Since its inception in 1965, Drugs of Today has established a reputation for excellence in providing physicians and other key healthcare professionals with practical, up-to-date monographs on recently approved and launched drugs.
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