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Clinical Trials and Observations: Eight-year experience with allogeneic stem cell transplantation for relapsed follicular lymphoma after nonmyeloablative conditioning with fludarabine cyclophosphamide and rituximab

机译:临床试验和观察:氟达拉滨环磷酰胺和利妥昔单抗非清髓性调理后同种异体干细胞移植治疗复发性滤泡性淋巴瘤已有八年经验

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摘要

Nonmyeloablative stem cell transplantation in patients with follicular lymphoma has been designed to exploit the graft-versus-lymphoma immunity. The long-term effectiveness and toxicity of this strategy, however, is unknown. In this prospective study, we analyzed our 8-year experience. Patients received a conditioning regimen of fludarabine (30 mg/m2 daily for 3 days), cyclophosphamide (750 mg/m2 daily for 3 days), and rituximab (375 mg/m2 for 1 day plus 1000 mg/m2 for 3 days). They were then given an infusion of human leukocyte antigen-matched hematopoietic cells from related (n = 45) or unrelated donors (n = 2). Tacrolimus and methotrexate were used for graft-versus-host disease (GVHD) prophylaxis. Forty-seven patients were included. All patients experienced complete remission, with only 2 relapses. With a median follow-up time of 60 months (range, 19-94), the estimated survival and progression-free survival rates were 85% and 83%, respectively. All 18 patients who were tested and had evidence of JH/bcl-2 fusion transcripts in the bone marrow at study entry experienced continuous molecular remission. The incidence of grade 2-IV acute GVHD was 11%. Only 5 patients were still undergoing immunosuppressive therapy at the time of last follow-up. We believe that the described results are a step forward toward developing a curative strategy for recurrent follicular lymphoma.
机译:滤泡性淋巴瘤患者的非清髓性干细胞移植已被设计为利用移植物抗淋巴瘤免疫力。然而,这种策略的长期有效性和毒性尚不清楚。在这项前瞻性研究中,我们分析了我们8年的经验。患者接受氟达拉滨(每天30 mg / m 2 ,持续3天),环磷酰胺(每天750 mg / m 2 ,持续3天),利妥昔单抗(375)的调节方案mg / m 2 1天,再加上1000 mg / m 2 3天)。然后从相关的(n = 45)或无关的供体(n = 2)中给他们输注人白细胞抗原匹配的造血细胞。他克莫司和甲氨蝶呤用于预防移植物抗宿主病(GVHD)。包括四十七名患者。所有患者均完全缓解,仅2次复发。中位随访时间为60个月(范围19-94),估计生存率和无进展生存率分别为85%和83%。所有进入研究的18名患者在研究进入时在骨髓中都有JH / bcl-2融合转录物的证据,均经历了连续的分子缓解。 2-IV级急性GVHD的发生率为11%。在最后一次随访时,只有5例患者仍在接受免疫抑制治疗。我们认为,所描述的结果是朝着开发复发性滤泡性淋巴瘤的治疗策略迈出的一步。

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