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首页> 外文期刊>Transplantation Proceedings >Feasibility of second hematopoietic stem cell transplantation using reduced-intensity conditioning with fludarabine and melphalan after a failed autologous hematopoietic stem cell transplantation.
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Feasibility of second hematopoietic stem cell transplantation using reduced-intensity conditioning with fludarabine and melphalan after a failed autologous hematopoietic stem cell transplantation.

机译:自体造血干细胞移植失败后,使用氟达拉滨和美法仑降低强度进行第二次造血干细胞移植的可行性。

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摘要

This study was performed to determine the feasibility of second hematopoietic stem cell transplantation (HSCT) using reduced-intensity conditioning (RIC) with fludarabine and melphalan in patients with relapsed hematologic malignancies after a prior autologous HSCT. Twelve patients (multiple myeloma [n = 7], non-Hodgkin lymphoma [n = 3], and acute myeloid leukemia [n = 2] received allogeneic HSCT using RIC with fludarabine (25 mg/m(2) for 5 days) and melphalan (140 mg/m(2) for 1 day) after a failed autologous HSCT. The graft-versus-host disease (GVHD) prophylaxis consisted of cyclosporine plus a minidose of methotrexate. All patients achieved a neutrophil and platelet engraftment in a median 13.5 days and 17.5 days, respectively. The transplant-related mortality was 2 patients (16.7%). Grade II-IV acute GVHD and chronic extensive GVHD were noted in 4 (33.3%) and 1 patient (11.1%), respectively. Over a median follow-up duration of 376 days, 5 patients were alive without evidence of disease. The estimated nonrelapse mortality at 1 year was 28.4%. The estimated overall survival rate at 1 year was 58.3%, and the estimated event-free survival rate at 1 year was 41.7%. Allogeneic HSCT using RIC with fludarabine and melphalan appears to be feasible for a second HSCT in patients with relapsed hematologic malignancies after a failed autologous HSCT.
机译:这项研究的目的是确定在先行自体HSCT后复发性血液系统恶性肿瘤患者中,使用氟达拉滨和美法仑的减低强度调节(RIC)进行第二次造血干细胞移植(HSCT)的可行性。 12名患者(多发性骨髓瘤[n = 7],非霍奇金淋巴瘤[n = 3]和急性髓性白血病[n = 2])接受了RIC联合氟达拉滨(25 mg / m(2)治疗5天)的异基因HSCT治疗,自体HSCT失败后进行美法仑(140 mg / m(2),持续1天)。预防移植物抗宿主病(GVHD)包括环孢菌素和小剂量甲氨蝶呤。所有患者中位嗜中性粒细胞和血小板植入分别为13.5天和17.5天,与移植相关的死亡率为2例患者(16.7%),其中II-IV级急性GVHD和慢性广泛GVHD分别为4例(33.3%)和1例(11.1%)。中位随访时间为376天,有5例患者存活,没有疾病迹象,估计1年的非复发死亡率为28.4%,估计1年的总生存率为58.3%,估计为无事件生存率在1年时为41.7%。使用RIC与氟达拉滨和美法兰的同种异体HSCT似乎可行。自体HSCT失败后血液系统恶性肿瘤复发的第二次HSCT。

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