髓系白血病
Fms样酪氨酸激酶3
癌症研究
医学
突变
髓样
白血病
肿瘤科
药理学
生物
内科学
遗传学
基因
作者
Lukáš Górecki,Eva Řezníčková,Vladimı́r Kryštof,Martina Řezáčová,Martina Čečková,Jan Korábečný
标识
DOI:10.1080/13543776.2024.2446224
摘要
Recent patents highlight advances in the field of FLT3 inhibitors with a focus on overcoming resistance, improving selectivity and potency. Future strategies may include third-generation inhibitors such as type III allosteric inhibitors, irreversible inhibitors, or PROTACs. Personalized medicine approaches utilizing genetic profiling to tailor therapies are emphasized. Exploration of novel combination regimens with emerging therapies like CAR T-cell therapy, immune checkpoint inhibitors, and small molecules targeting critical AML pathways is ongoing to further enhance anti-leukemic efficacy.
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