Lun Y, Yang J-J, Wu Y
Department of Hematology and Hematology Research Laboratory, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Division of Molecular Bioregulation, Cancer Research Institute, Kanazawa University, Kanazawa, Ishikawa, Japan.
J Clin Pharm Ther. 2017 Dec;42(6):786-789. doi: 10.1111/jcpt.12577. Epub 2017 Jun 23.
The mixed lineage leukaemia (MLL) gene translocations are found in approximately 10% of adults with acute myeloid leukaemia (AML) and are markers of poor prognosis. As the best reported response in relapsed and refractory MLL-rearranged AML is around 40%, reinduction treatment is very challenging for those patients.
We report a case of relapsed and refractory AML with MLL-AF9, who did not respond to FLAG (fludarabine, cytarabine, granulocyte colony stimulating factor) regimen reinduction treatment, but achieved complete response and molecular remission after chidamide-based chemotherapy.
Chidamide (CS055/HBI-8000) is a new histone deacetylase (HDAC) inhibitor that is clinically active in relapsed and refractory peripheral T-cell lymphomas. To the best of our knowledge, successful reinduction treatment on relapsed MLL-AF9 by chidamide-based regimen has not been previously reported.
混合谱系白血病(MLL)基因易位在约10%的成年急性髓系白血病(AML)患者中被发现,是预后不良的标志物。由于复发难治性MLL重排AML的最佳报道缓解率约为40%,因此对这些患者进行再诱导治疗极具挑战性。
我们报告1例伴有MLL-AF9的复发难治性AML患者,其对FLAG(氟达拉滨、阿糖胞苷、粒细胞集落刺激因子)方案再诱导治疗无反应,但在基于西达本胺的化疗后实现了完全缓解和分子缓解。
西达本胺(CS055/HBI-8000)是一种新型组蛋白去乙酰化酶(HDAC)抑制剂,在复发难治性外周T细胞淋巴瘤中具有临床活性。据我们所知,此前尚未有基于西达本胺方案成功对复发的MLL-AF9进行再诱导治疗的报道。