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Treatment strategies in patients with AML or high-risk myelodysplastic syndrome relapsed after Allo-SCT

机译:Allo-SCT后复发的AML或高危骨髓增生异常综合征患者的治疗策略

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Non-relapse mortality after Allo-SCT has significantly decreased over the last years. Nevertheless, relapse remains a major cause for post SCT mortality in patients with AML and high-risk myelodysplastic syndrome (MDS). In this retrospective single-center analysis, we have analyzed the treatment outcomes of 108 patients with AML or MDS, who relapsed after Allo-SCT. Seventy of these patients (65%) were treated with salvage therapies containing chemotherapy alone, allogeneic cell-based treatment or the combination of both. Thirty-eight patients (35%) received palliative treatment. Median OS after diagnosis of relapse was 130 days. Compared with patients who received chemotherapy alone, response to salvage therapy was significantly improved in patients treated with a combination of chemo-and allogeneic cell-based therapy (CR rate 57% vs 13%, P = 0.002). Among risk factors concerning pretreatment characteristics, disease status before first Allo-SCT, and details of transplantation, only the time interval from Allo-SCT to relapse was an independent predictor of response to salvage therapy and OS. These data confirmed that time to relapse after transplantation is an important prognostic factor. Up to now, only patients eligible for treatment regimens containing allogeneic cell-based interventions achieved relevant response rates.
机译:在过去的几年中,Allo-SCT后的非复发死亡率显着降低。然而,复发仍然是AML和高危骨髓增生异常综合征(MDS)患者SCT术后死亡率的主要原因。在这项回顾性单中心分析中,我们分析了108例Allo-SCT术后复发的AML或MDS患者的治疗结果。这些患者中有七十名(65%)接受了仅包含化学疗法,基于异基因细胞的治疗或两者结合的挽救疗法。 38位患者(35%)接受了姑息治疗。诊断为复发后的中位OS为130天。与仅接受化学疗法的患者相比,采用化学和异体细胞治疗的患者对挽救疗法的反应显着改善(CR率分别为57%和13%,P = 0.002)。在与预处理特征,首次Allo-SCT之前的疾病状态以及移植细节有关的危险因素中,只有从Allo-SCT到复发的时间间隔是对挽救疗法和OS反应的独立预测因子。这些数据证实,移植后复发时间是重要的预后因素。迄今为止,只有符合包含异基因细胞干预措施的治疗方案的患者才有相关的缓解率。

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