克拉屈滨
医学
戊抑素
毛细胞白血病
嘌呤类似物
威罗菲尼
核苷类似物
伊布替尼
苯达莫司汀
美罗华
曲美替尼
肿瘤科
白血病
达布拉芬尼
药理学
慢性淋巴细胞白血病
内科学
癌症研究
核苷
嘌呤
淋巴瘤
MAPK/ERK通路
黑色素瘤
激酶
化学
酶
细胞生物学
生物
立体化学
生物化学
转移性黑色素瘤
作者
Aditya Sarvaria,Zheng Topp,Alan Saven
出处
期刊:JAMA Oncology
[American Medical Association]
日期:2015-10-29
卷期号:2 (1): 123-123
被引量:29
标识
DOI:10.1001/jamaoncol.2015.4134
摘要
Hairy cell leukemia (HCL) is a chronic B-cell leukemia noted for an indolent course that ultimately results in cytopenias and massive splenomegaly. Whereas treatment with the nucleoside purine analogues cladribine and pentostatin results in lengthy remissions in nearly all patients with HCL, most patients will experience relapse while a small percentage of patients' disease fails to respond to therapy in the first place. Retreatment with a purine nucleoside analogue often leads to an effective but limited response. For decades, few other viable therapeutic options were available to these patients who required retreatment. Recently, new insights into the mechanism of disease of HCL have led to research in new potential treatment agents, either alone or with a purine nucleoside analogue. Clinical trials with rituximab, bendamustine, and conjugate immunotoxins will reveal what role these therapies will have in HCL treatment. A better understanding of the BRAF/MEK/ERK pathway and the B-cell signaling pathway has allowed further exploration into the novel drugs vemurafenib, dabrafenib, trametinib, and ibrutinib.
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