全身性肥大细胞增多症
医学
米多司他林
伊马替尼
全身疗法
药理学
免疫学
疾病
内科学
白血病
髓系白血病
癌症
乳腺癌
作者
Giovanni Costanzo,Valentina Marzio,Edoardo Cavaglià,Giovanni Paoletti,Enrico Heffler
标识
DOI:10.1097/aci.0000000000001079
摘要
Despite the considerable therapeutic progress in recent years, systemic mastocytosis is an incurable disease. In the last 20 years, the management of systemic mastocytosis has transformed from a one-size-fits-all approach, characterized by nonspecific cytoreductive drugs, to a tailored strategy focused on increasingly precise molecular targets, with the most notable example being the KIT inhibitors. Recently, the FDA and EMA have approved two drugs for treating systemic mastocytosis: avapritinib and midostaurin. Moreover, numerous trials are currently assessing the efficacy of new molecules: most are testing new-generation KIT inhibitors (ripretinib, bezuclastinib, elenestinib, masitinib, nintedanib), others focusing on Bruton's kinase (TL-895), interleukin-6 (sarilumab), sialic acid-binding immunoglobulin-like lectin-8 (lirentelimab), mTOR and CD33, among others. Real-life data are needed to confirm preliminary preclinical results.
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