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Multicenter phase 1 trial of intraventricular immunochemotherapy in recurrent CNS lymphoma

机译:脑室内免疫化学疗法治疗复发性中枢神经系统淋巴瘤的多中心1期试验

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Recurrent CNS lymphoma continues to be associated with poor outcomes in the rituximab era. Although IV rituximab mediates superior disease control of systemic non-Hodgkin lymphoma (NHL), it fails to completely eliminate the risk of meningeal recurrence, likely due to minimal CNS penetration. Given that rituximab acts synergistically with chemotherapy, we conducted the first phase 1 study of intraventricular immunochemotherapy in patients with recurrent CNS NHL. Fourteen patients received 10 mg or 25 mg intraventricular rituximab twice weekly for 4 weeks, with rituximab administered as monotherapy during the first treatment each week and rituximab administered in combination with methotrexate (MTX) during the second treatment each week. More than 150 doses were administered without serious toxicity. In a population with high-refractory CNS NHL, 75% of patients achieved complete cytologic responses and 43% achieved an overall complete response in CSF and/or brain parenchyma. Two patients achieved a first complete response of CNS NHL with intraventricular rituximab/MTX, including 1 with CNS lymphoma refractory to high-dose systemic and intrathecal MTX plus IV rituximab. We conclude that intraventricular rituximab in combination with MTX is feasible and highly active in the treatment of drug-resistant CNS NHL that is refractory or unresponsive to IV rituximab. This trial is registered at www.clinicaltrials.gov as NCT00221325.
机译:中枢神经系统淋巴瘤复发仍与利妥昔单抗时代的不良预后相关。尽管IV利妥昔单抗介导了系统性非霍奇金淋巴瘤(NHL)的卓越疾病控制,但它可能无法完全消除脑膜复发的风险,这可能是由于中枢神经系统渗透率最低。鉴于利妥昔单抗与化学疗法协同作用,我们对复发性中枢神经系统非霍奇金淋巴瘤患者进行了脑室内免疫化学疗法的第一个1期研究。 14名患者每周两次接受10 mg或25 mg脑室内利妥昔单抗治疗,持续4周,每周一次在第一次治疗中给予利妥昔单抗单药治疗,每周第二次治疗期间利妥昔单抗与甲氨蝶呤(MTX)联用。给予超过150剂剂量,无严重毒性。在具有高难治性中枢神经系统NHL的人群中,有75%的患者在CSF和/或脑实质中获得了完全的细胞学应答,而43%的患者获得了完全的完全应答。两名患者在脑室内应用利妥昔单抗/ MTX首次实现了CNS NHL的完全缓解,其中1例对大剂量全身和鞘内MTX加静脉注射利妥昔单抗难治的CNS淋巴瘤。我们得出结论,脑室内利妥昔单抗联合MTX是可行的,并且在治疗难治性或对IV利妥昔单抗无反应的耐药性CNS NHL中具有很高的活性。该试验已在www.clinicaltrials.gov上注册为NCT00221325。

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