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Improved outcome of adult Burkitt lymphoma/leukemia with rituximab and chemotherapy: report of a large prospective multicenter trial

机译:利妥昔单抗和化疗的成人Burkitt淋巴瘤/白血病的改善结果:大型前瞻性多中心试验的报告

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摘要

This largest prospective multicenter trial for adult patients with Burkitt lymphoma/leukemia aimed to prove the efficacy and feasibility of short-intensive chemotherapy combined with the anti-CD20 antibody rituximab. From 2002 to 2011, 363 patients 16 to 85 years old were recruited in 98 centers. Treatment consisted of 6 5-day chemotherapy cycles with high-dose methotrexate, high-dose cytosine arabinoside, cyclophosphamide, etoposide, ifosphamide, corticosteroids, and triple intrathecal therapy. Patients >55 years old received a reduced regimen. Rituximab was given before each cycle and twice as maintenance, for a total of 8 doses. The rate of complete remission was 88% (319/363); overall survival (OS) at 5 years, 80%; and progression-free survival, 71%; with significant difference between adolescents, adults, and elderly patients (OS rate of 90%, 84%, and 62%, respectively). Full treatment could be applied in 86% of the patients. The most important prognostic factors were International Prognostic Index (IPI) score (0-2 vs 3-5; P=.0005), age-adjusted IPI score (0-1 vs 2-3; P=.0001), and gender (male vs female; P=.004). The high cure rate in this prospective trial with a substantial number of participating hospitals demonstrates the efficacy and feasibility of chemoimmunotherapy, even in elderly patients. This trial was registered at www.clinicaltrials.gov as #NCT00199082.
机译:这种最大的预期多中心试验,用于Burkitt淋巴瘤/白血病的成人患者,旨在证明短期化化疗与抗CD20抗体利妥昔单抗相结合的疗效和可行性。从2002年到2011年,在98个中心招募了363名患者16至85岁。治疗由6个5日的化疗循环组成,具有高剂量甲氨蝶呤,高剂量胞嘧啶阿拉伯苷,环磷酰胺,依托泊苷,Ifosphamide,皮质类固醇和三重鞘内治疗。患者> 55岁接受了减少的方案。 Rituximab在每个循环之前给出,两次作为维护,总共8剂。完全缓解率为88%(319/363);总生存(OS)在5年,80%;和无进展的生存率,71%;青少年,成人和老年患者(OS率分别为90%,84%和62%)之间具有显着差异。可以在86%的患者中适用全面治疗。最重要的预后因素是国际预后指数(IPI)得分(0-2与3-5; P = .0005),年龄调整的IPI评分(0-1 vs 2-3; p = .0001),以及性别(男性vs女; p = .004)。这种前瞻性审判中的高治愈率,其中大量参与医院甚至在老年患者中表明了化疗疗法的疗效和可行性。此试验在www.clinicaltrials.gov注册为#nct00199082。

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