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Pilot Trial of Systemic Methotrexate plus R-CHOP Regimen with Intrathecal Methotrexate for Simultaneous Central Nervous System and Systemic Diffuse Large B Cell Lymphoma

机译:系统性甲氨蝶呤加R-CHOP方案鞘内注射甲氨蝶呤治疗中枢神经系统和全身弥漫性大B细胞淋巴瘤的试验

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Background: The simultaneous presentation of systemic diffuse large B cell lymphoma (DLBCL) with central nervous system (CNS) disease is not well controlled by either R-CHOP or systemic methotrexate (MTX) alone. Methods: We conducted a pilot trial with 6 patients who were initially diagnosed with systemic DLBCL with CNS involvement. Patients were treated with a systemic MTX plus R-CHOP regimen. Results: The overall response rate was 4/6 (66.7%). The CNS response rate and systemic response rate were 4/6 (66.7%) and 5/6 (83.3%), respectively. The median response duration of the 4 patients with complete remission at completion was 25.5 months, and the median survival of all patients was 25.1 months. CNS lesions progressed in all relapsed and refractory patients, while systemic disease progression was observed in 1 patient. No fatal hematologic adverse effects, hepatotoxicity or nephrotoxicity were observed. Conclusions: The dose of systemic MTX (1 similar to 1.5 g/m(2)) or dose intensity (4-week interval in 4 patients) used in this trial was considered insufficient. Therefore, the dose of MTX or interval of each chemotherapy cycle should be modified in future trials to control CNS disease involved with DLBCL. (C) 2014 S. Karger AG, Basel
机译:背景:全身性弥漫性大B细胞淋巴瘤(DLBCL)与中枢神经系统(CNS)疾病的同时出现,不能通过R-CHOP或全身性甲氨蝶呤(MTX)很好地控制。方法:我们对6例最初诊断为中枢神经系统受累的系统性DLBCL的患者进行了一项试验性研究。患者接受全身性MTX加R-CHOP方案治疗。结果:总体回应率为4/6(66.7%)。中枢神经系统反应率和全身反应率分别为4/6(66.7%)和5/6(83.3%)。 4名完成缓解后完全缓解的患者的中位反应持续时间为25.5个月,所有患者的中位生存期为25.1个月。所有复发性和难治性患者的中枢神经系统病变进展,而1例患者观察到全身性疾病进展。没有观察到致命的血液学不良反应,肝毒性或肾毒性。结论:该试验中使用的全身性MTX剂量(1类似于1.5 g / m(2))或剂量强度(4名患者每4周间隔一次)被认为不足。因此,在以后的试验中应调整MTX剂量或每个化疗周期的间隔,以控制与DLBCL有关的CNS疾病。 (C)2014 S.Karger AG,巴塞尔

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