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Sorafenib in relapsed and refractory FLT3-ITD positive acute myeloid leukemia: a novel treatment option

机译:索拉非尼治疗复发性和难治性FLT3-ITD阳性急性髓性白血病:一种新的治疗选择

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BACKGROUND: The therapeutic options for relapsed or refractory FLT3-ITD positive AML are limited, particularly in case of a prior allogenic stem cell transplantation (SCT) or poor performance status. The clinical value of a targeted intervention using the FLT3-ITD-specific inhibitor sorafenib in this situation is largely unknown. PATIENTS AND METHODS: Between 2007 and 2010 eight patients (4 men, 4 women; age 40-75 years) with relapsed or refractory FLT3-ITD positive acute myeloid leukemia (AML) before (n=4) and after allogenic SCT (n=5) were treated off-label with sorafenib. RESULTS: All patients showed rapid hematological responses. There were three complete molecular remissions when sorafenib was given after allogenic SCT. Two of them are ongoing for 12 and 15 months, respectively. Long-term remissions after prior allogenic SCT were associated with the re-establishment of a chronic graft versus host reaction. Side effects could be controlled by dose reduction. CONCLUSION: Sorafenib is apparently an effective treatment alternative for patients with relapsed or refractory FLT3-ITD positive AML. In the context of a prior allogenic SCT it may have curative potential via inducing a synergism between targeted inhibition of FLT3-ITD and anti-leukemic immunity.
机译:背景:复发性或难治性FLT3-ITD阳性AML的治疗选择有限,特别是在先前的同种异体干细胞移植(SCT)或不良状态的情况下。在这种情况下使用FLT3-ITD特异性抑制剂索拉非尼进行靶向干预的临床价值尚不清楚。患者与方法:在2007年至2010年之间,有8例(4例男性,4例女性;年龄40-75岁)在异基因SCT之前(n = 4)和之后发生了复发性或难治性FLT3-ITD阳性急性髓细胞白血病(AML)(n = 5)用索拉非尼超标治疗。结果:所有患者均表现出快速的血液学反应。同种异体SCT后给予索拉非尼有3个完全的分子缓解。其中两个分别进行了12个月和15个月。先前同种异体SCT术后的长期缓解与慢性移植物抗宿主反应的重建有关。副作用可以通过减少剂量来控制。结论:索拉非尼显然是复发或难治性FLT3-ITD阳性AML患者的有效治疗选择。在先前的同种异体SCT的背景下,它可能通过诱导FLT3-ITD的靶向抑制与抗白血病免疫之间的协同作用而具有治疗潜力。

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