作者: Tor Henrik Tvedt , Ina Nepstad , Øystein Bruserud
DOI: 10.1080/13543784.2017.1275564
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摘要: ABSTRACTIntroduction: Midostaurin is a multikinase inhibitor that inhibits receptor tyrosine kinases (Flt3, CD117/c-kit, platelet-derived growth factor receptor, vascular endothelial 2) as well non-receptor (Frg, Src, Syk, Protein kinase C). Combination of midostaurin with conventional intensive chemotherapy followed by one year maintenance monotherapy was recently reported to improve the survival acute myeloid leukemia (AML) patients Flt3 mutations.Areas covered: Relevant publications were identified through literature searches in PubMed database. We searched for (i) original articles describing results from clinical studies; (ii) published importance midostaurin-inhibited leukemogenesis and chemosensitivity.Expert opinion: tolerated, combined gastrointestinal toxicity increases significantly. alters anthracycline pharmacokinetics. Fu...