首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Repeat treatment with iodine-131-rituximab is safe and effective in patients with relapsed indolent B-cell non-Hodgkin's lymphoma who had previously responded to iodine-131-rituximab.
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Repeat treatment with iodine-131-rituximab is safe and effective in patients with relapsed indolent B-cell non-Hodgkin's lymphoma who had previously responded to iodine-131-rituximab.

机译:碘131-利妥昔单抗重复治疗对先前对碘131-利妥昔单抗有反应的复发性惰性B细胞非霍奇金淋巴瘤复发患者是安全有效的。

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BACKGROUND: Small series suggest retreatment of indolent lymphomas with murine anti-CD20 radioimmunotherapy is effective. The longer half-life of iodine-131 ((131)I)-rituximab may result in increased bone marrow exposure, with greater toxicity on repeat administration. We examined the effects of a second (131)I-rituximab in patients with indolent lymphoma following relapse. PATIENTS AND METHODS: We analyzed two institutional databases from January 2000 to July 2007 for retreatment with (131)I-rituximab. The severity of cytopenia, development of myelodysplasia (MDS), acute myeloid leukemia (AML) and hypothyroidism was noted. We compared response duration and toxicity of the treatments. RESULTS: Fourteen of 16 patients responded with nine complete responses (CRs), with a median duration of 10.5 months in responders. Six of 13 reresponders had the same or a longer response and six more remain in complete response. The median event-free survival was not significantly different for the two treatments. Therewas no significant difference in the severity of myelosuppression. Four patients developed hypothyroidism with three requiring thyroxine. One patient developed AML, with no other cases of MDS. The actuarial progression-free survival rate at 12 months was 36%. CONCLUSIONS: Repeat (131)I-rituximab induces high response rates, some of which result in durable remissions in patients who had previously responded.
机译:背景:小系列研究表明,用鼠抗CD20放射免疫疗法治疗惰性淋巴瘤是有效的。碘131((131)I)-利妥昔单抗的半衰期较长,可能导致骨髓暴露增加,重复给药具有更大的毒性。我们检查了复发性惰性淋巴瘤患者第二次(131)I-利妥昔单抗的治疗效果。患者与方法:我们分析了2000年1月至2007年7月用于(131)I-利妥昔单抗复治的两个机构数据库。记录了严重的血细胞减少症,骨髓增生异常(MDS),急性髓细胞性白血病(AML)和甲状腺功能减退症。我们比较了治疗的反应时间和毒性。结果:16例患者中有14例有9例完全缓解(CR),响应者中位持续时间为10.5个月。 13位响应者中有6位具有相同或更长的响应,另外6位仍保持完整响应。两种治疗的中位无事件生存期无显着差异。骨髓抑制的严重程度没有显着差异。四名患者出现甲状腺功能减退,三名需要甲状腺素。一名患者患有AML,没有其他MDS病例。 12个月时精算无进展生存率为36%。结论:重复(131)I-利妥昔单抗诱导高反应率,其中一些导致先前有反应的患者持续缓解。

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