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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Lenalidomide maintenance after nonmyeloablative allogeneic stem cell transplantation in multiple myeloma is not feasible: results of the HOVON 76 Trial.
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Lenalidomide maintenance after nonmyeloablative allogeneic stem cell transplantation in multiple myeloma is not feasible: results of the HOVON 76 Trial.

机译:非清髓性异体干细胞移植治疗多发性骨髓瘤后来那度胺的维持是不可行的:HOVON 76试验的结果。

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摘要

To improve the outcome of allogeneic stem cell transplantation (allo-SCT) in multiple myeloma as part of first-line treatment, we prospectively investigated the feasibility and efficacy of lenalidomide maintenance. Patients started maintenance 1 to 6 months after nonmyeloablative allo-SCT. Lenalidomide was dosed 10 mg on days 1 to 21 of a 28-day schedule for a total of 24 cycles. Peripheral blood samples were taken to evaluate immune modulating effects. Thirty-five eligible patients were enrolled, and 30 started with lenalidomide. After 2 cycles, 14 patients (47%) had to stop treatment, mainly because of the development of acute graft versus host disease (GVHD). In total, 13 patients (43%) stopped treatment because of development of GVHD, 5 patients (17%) because of other adverse events, and 5 patients (17%) because of progression. Responses improved in 37% of patients, and the estimated 1-year progression-free survival from start of maintenance was 69% (90% confidence interval, 53%-81%). Lenalidomide increased the frequency of human leukocyte antigen-DR(+) T cells and regulatory T cells, without correlation with clinical parameters. In conclusion, lenalidomide maintenance 10 mg daily after nonmyeloablative allo-SCT with unmanipulated graft in multiple myeloma patients is not feasible, mainly because of the induction of acute GVHD. This trial was registered at www.trialregister.nl as #NTR1645.
机译:为了改善多发性骨髓瘤同种异体干细胞移植(allo-SCT)的治疗效果,作为一线治疗的一部分,我们前瞻性研究了来那度胺维持的可行性和疗效。非清髓性异体SCT术后1至6个月,患者开始维持治疗。来那度胺在28天的治疗计划的第1到21天服用10 mg,共24个周期。采集外周血样品以评估免疫调节作用。入选了35例合格患者,其中30例开始使用来那度胺。 2个周期后,有14名患者(47%)必须停止治疗,这主要是由于急性移植物抗宿主病(GVHD)的发展。总共有13例患者(43%)因发生GVHD而停止治疗,5例患者(17%)因其他不良事件而停止治疗,5例患者(17%)因进展而停止。 37%的患者的反应有所改善,并且从维持治疗开始的1年无进展生存期估计为69%(90%置信区间,53%-81%)。来那度胺增加人白细胞抗原-DR(+)T细胞和调节性T细胞的频率,而与临床参数无关。总之,在多发性骨髓瘤患者中进行非清髓性异体-SCT联合非操作性移植后,来那度胺每天维持10 mg的治疗是不可行的,这主要是因为诱导了急性GVHD。该试验已在www.trialregister.nl注册为#NTR1645。

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