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首页> 外文期刊>Current opinion in pediatrics >The efficacy of rituximab in high-grade pediatric B-cell lymphoma/leukemia: a review of available evidence.
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The efficacy of rituximab in high-grade pediatric B-cell lymphoma/leukemia: a review of available evidence.

机译:利妥昔单抗在小儿高度B细胞淋巴瘤/白血病中的疗效:现有证据综述。

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PURPOSE OF REVIEW: This review evaluates whether rituximab has efficacy in high-grade pediatric B-cell lymphoma/leukemia. Current pediatric protocols for CD20+ B-cell lymphoma/leukemia significantly improve survival, but with major morbidity. To assess whether rituximab has efficacy in very high-grade pediatric disease, all published data on rituximab therapy for Burkitt's lymphoma/B acute lymphoblastic leukaemia (B-ALL) and pediatric patients with relapsed/refractory large B-cell lymphoma were reviewed. RECENT FINDINGS: Three trials in adult Burkitt's/B-ALL showed a significant survival advantage when rituximab was added to standard chemotherapy. Minimal pediatric data have been published, but 19 children with mature B-cell lymphoma/B-ALL received rituximab, alone or in combination with chemotherapy, as salvage therapy, after failure of intensive chemotherapy. Fifteen of 19 (79%) responded, 12 (63%) remained alive in continuous complete remission at 5+ to 48+ months of follow-up. Two patients were alive in partial remission. Five patients died, four of progressive disease. Only one patient had no response to rituximab. SUMMARY: Rituximab has demonstrated efficacy in Burkitt's disease in adults. Although positive reporting bias is suspected, it appears that rituximab, even as monotherapy, has efficacy in heavily pretreated pediatric patients with high-grade B-lymphoma/B-ALL. Rituximab use can be justified in a prospective controlled chemotherapy dose-reduction study.
机译:审查的目的:这篇综述评估了利妥昔单抗在高等级儿科B细胞淋巴瘤/白血病中是否具有疗效。当前针对CD20 + B细胞淋巴瘤/白血病的儿科治疗方案可显着提高生存率,但发病率较高。为了评估利妥昔单抗在极度高度的儿科疾病中是否具有疗效,回顾了所有已发表的有关利妥昔单抗治疗伯基特淋巴瘤/ B急性淋巴细胞白血病(B-ALL)和复发/难治性大B细胞淋巴瘤的儿科患者的数据。最近的发现:在成人Burkitt / B-ALL中进行的三项试验表明,将利妥昔单抗加入标准化疗后具有显着的生存优势。很少的儿科数据已经公布,但是19例成熟的B细胞淋巴瘤/ B-ALL患儿在强化化疗失败后,单独或联合化疗接受了利妥昔单抗作为挽救疗法。 19例中有15例(79%)有反应,在5个月至48个月以上的随访中,12例(63%)持续完全缓解仍存活。 2例患者部分缓解还活着。五名患者死亡,四名进行性疾病。只有一名患者对利妥昔单抗无反应。摘要:利妥昔单抗已证明对成人伯基特氏病有效。尽管怀疑有积极的报告偏倚,但似乎利妥昔单抗,即使作为单一疗法,也对经过高度预处理的小儿高级别B淋巴瘤/ B-ALL患者有效。利妥昔单抗的使用可以在前瞻性控制化疗的减量研究中证明是正确的。

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