首页> 外文期刊>Hematological oncology >Treatment of secondary central nervous system lymphoma with intrathecal rituximab, high‐dose methotrexate, and R‐DHAP followed by autologous stem cell transplantation: results of the HOVON 80 phase 2 study
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Treatment of secondary central nervous system lymphoma with intrathecal rituximab, high‐dose methotrexate, and R‐DHAP followed by autologous stem cell transplantation: results of the HOVON 80 phase 2 study

机译:用鞘内蓖麻毒素,高剂量甲氨蝶呤和R-DHAP治疗次级中枢神经系统淋巴瘤,然后进行自体干细胞移植:HOVON 80阶段2研究的结果

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Abstract The prognosis of central nervous system (CNS) relapse of systemic non‐Hodgkin lymphoma is poor with 1‐year survival historically at 0% to 20%. Aiming to improve these results, we performed a multicenter phase 2 study in patients with a CNS relapse, with or without concurrent systemic relapse. Treatment consisted of 2?cycles of R‐DHAP alternating with high‐dose methotrexate (MTX) and was combined with intrathecal rituximab. Responding patients received a third R‐DHAP‐MTX cycle followed by busulfan and cyclophosphamide myeloablative therapy and autologous stem cell transplantation. In patients with persistent cerebrospinal fluid lymphoma after cycle 1, the intrathecal rituximab was replaced by intrathecal triple therapy, with MTX, cytarabine, and dexamethasone. Thirty‐six patients were included. Eighteen had evidence of cerebrospinal fluid lymphoma, 24 had brain parenchymal disease, and 20 (56%) had concurrent systemic disease. The overall response rate after 2 R‐DHAP‐MTX was 53% (19/36), with 22% (8/36) complete remission. Fifteen patients (42%) underwent a transplant. One‐year progression‐free survival was 19% (95% confidence interval, 9‐34): 25% in patients without and 15% in patients with systemic disease. One‐year overall survival was 25% (95% confidence interval, 12‐40). This treatment regimen did not result in a major improvement of outcome of secondary CNS lymphoma, especially when concurrent systemic disease was present. Registered in the Dutch trial register www.trialregister.nl , NTR1757; EudraCT number 2006‐002141‐37.
机译:摘要中枢神经系统(CNS)拷贝全身性非霍奇金淋巴瘤的预后较差,1年生存历史上涨0%至20%。旨在改善这些结果,我们对CNS复发的患者进行了多中心第2期研究,有或没有并发全身复发。治疗由2?与高剂量甲氨蝶呤(MTX)交替的R-DHAP循环,并与鞘内蓖麻人合并。响应患者接受了第三个R-DHAP-MTX周期,然后是Busulfan和环磷酰胺肌钙糖治疗和自体干细胞移植。在循环1后持续脑脊液淋巴瘤的患者中,鞘内蓖麻毒素以鞘内三重疗法取代,用MTX,Cytarabine和地塞米松代替。包括三十六名患者。十八有脑脊液淋巴瘤的证据,24例脑实质疾病,20(56%)进行了同时的全身疾病。 2R-DHAP-MTX后的整体反应率为53%(19/36),22%(8/36)完全缓解。十五名患者(42%)正在进行移植。一年的无进展生存率为19%(95%置信区间,9-34):患者25%,全身疾病患者患者有15%。一年的总生存率为25%(95%置信区间,12-40)。这种治疗方案没有导致继发性CNS淋巴瘤结果的重大改进,特别是当存在并发全身性疾病时。注册在荷兰试用注册www.trialRegister.nl,NTR1757; eudract 2006-002141-37。

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