钇-90 ibrumomab tixetan + busulfan,环磷酰胺和依托泊苷(BuCyE)与单独BuCyE作为非霍奇金淋巴瘤的调理方案。

The Korean Journal of Hematology Pub Date : 2012-06-01 Epub Date: 2012-06-26 DOI:10.5045/kjh.2012.47.2.119
Jae-Cheol Jo, Dok Hyun Yoon, Shin Kim, Jung Sun Park, Chan-Sik Park, Jooryung Huh, Sang-Wook Lee, Jin-Sook Ryu, Cheolwon Suh
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引用次数: 8

摘要

背景:放射免疫治疗药物在自体干细胞移植中具有非常重要的作用,因为它们可以改善耐受性并增加调理方案的疗效。方法:回顾性分析ybrumomab tiuxetan (Zevalin)联合静脉注射busulfan、环磷酰胺和依托泊苷(Z-BuCyE)治疗复发或难治性b细胞非霍奇金淋巴瘤(NHL)患者的疗效和毒性,并与单独使用BuCyE后自体干细胞移植进行比较。比较了19例接受Z-BuCyE治疗的患者和19例接受BuCyE治疗的历史对照组的疗效、毒性和植入特性。结果:两个治疗组具有相似的基线特征。血小板植入(>20×10(9)/L)和中性粒细胞植入(>0.5×10(9)/L)的中位时间在Z-BuCyE组(分别为12天和10天)和BuCyE组(分别为12天和10天)之间无显著差异。在毒性和治疗相关死亡率方面,两组间未观察到显著差异。中位随访时间为30.4个月,Z-BuCyE组的中位无事件生存期(12.5个月)普遍优于BuCyE组(6.2个月,P=0.236)。两组间的总生存率无显著差异。结论:在BuCyE大剂量化疗中加入伊布单抗替克坦可能使复发或难治性b细胞NHL患者受益,且无额外毒性风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Yttrium-90 ibritumomab tiuxetan plus busulfan, cyclophosphamide, and etoposide (BuCyE) versus BuCyE alone as a conditioning regimen for non-Hodgkin lymphoma.

Background: Radioimmunotherapy agents have a highly significant role in autologous stem cell transplantation as they improve tolerability and increase the efficacy of the conditioning regimen.

Methods: We retrospectively analyzed the efficacy and toxicity of yttrium-90 ibritumomab tiuxetan (Zevalin) combined with intravenous busulfan, cyclophosphamide, and etoposide (Z-BuCyE) compared with those of BuCyE alone followed by autologous stem cell transplantation in patients with relapsed or refractory B-cell non-Hodgkin lymphoma (NHL). The efficacy, toxicity, and engraftment characteristics were compared between 19 patients who received Z-BuCyE and 19 historical controls who received BuCyE.

Results: The 2 treatment groups shared similar baseline characteristics. The median time to platelet engraftment (>20×10(9)/L) and neutrophil engraftment (>0.5×10(9)/L) did not significantly differ between the Z-BuCyE group (12 days and 10 days, respectively) and the BuCyE group (12 days and 10 days, respectively). No significant differences were observed between the groups with respect to toxicities and treatment-related mortality. The median follow-up period was 30.4 months, and median event-free survival was generally better in the Z-BuCyE group (12.5 months) vs. the BuCyE group (6.2 months, P=0.236). No significant difference in overall survival between the groups was noted.

Conclusion: Adding ibritumomab tiuxetan to BuCyE high-dose chemotherapy may benefit patients with relapsed or refractory B-cell NHL with no risk of additional toxicity.

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