米多司他林
医学
索拉非尼
舒尼替尼
髓系白血病
肿瘤科
内科学
血液学
癌症研究
药理学
癌症
肝细胞癌
作者
Mei‐Hwan Wu,Chuntuan Li,Xiongpeng Zhu
标识
DOI:10.1186/s13045-018-0675-4
摘要
FLT3 mutations are one of the most common findings in acute myeloid leukemia (AML). FLT3 inhibitors have been in active clinical development. Midostaurin as the first-in-class FLT3 inhibitor has been approved for treatment of patients with FLT3-mutated AML. In this review, we summarized the preclinical and clinical studies on new FLT3 inhibitors, including sorafenib, lestaurtinib, sunitinib, tandutinib, quizartinib, midostaurin, gilteritinib, crenolanib, cabozantinib, Sel24-B489, G-749, AMG 925, TTT-3002, and FF-10101. New generation FLT3 inhibitors and combination therapies may overcome resistance to first-generation agents.
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