医学
阿糖胞苷
耐火材料(行星科学)
髓系白血病
阿扎胞苷
内科学
柔红霉素
Fms样酪氨酸激酶3
维持疗法
肿瘤科
白血病
外科
化疗
生物
突变
生物化学
基因表达
天体生物学
基因
DNA甲基化
作者
Giulia Arrigo,Stefano D’Ardìa,Ernesta Audisio,Marco Cerrano,Roberto Freilone,Valentina Giai,Carolina Secreto,Irene Urbino,Chiara Frairia
摘要
Extramedullary relapse of acute myeloid leukemia (AML) is not a rare event, and the FMS-like tyrosine kinase 3 (<i>FLT3</i>) mutation is a well-known risk factor. Gilteritinib is approved for relapsed/refractory <i>FLT3</i>+ AML, but its efficacy in extramedullary relapse is still undefined. Here, we present the case of a 69-year-old woman with therapy-related nucleophosmin-1 and <i>FLT3</i>-internal tandem duplication (<i>FLT3</i>-ITD) positive AML treated with induction and consolidation with CPX-351 (liposomal daunorubicin plus cytarabine) followed by off-label azacitidine maintenance who obtained a complete remission (CR) with persistent measurable residual disease. After 19 months of CR, she experienced an isolated breast relapse of <i>FLT3</i>-ITD+ AML. She was started on single-agent gilteritinib, resulting in a rapid and persistent complete regression of the breast nodule. Targeted therapy with gilteritinib for relapsed/refractory <i>FLT3</i>-ITD+ AML can be effective in isolated extramedullary relapse.
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