High-Dose Methotrexate-Based Chemotherapy Followed by Consolidating Radiotherapy in Non–AIDS-Related Primary Central Nervous System Lymphoma: European Organization for Research and Treatment of Cancer Lymphoma Group Phase II Trial 20962

医学 卡莫司汀 化疗 甲基强的松龙 内科学 外科 阿糖胞苷 甘薯糖苷 放射治疗 甲氨蝶呤 养生 胃肠病学 化疗方案 原发性中枢神经系统淋巴瘤 环磷酰胺 依托泊苷
作者
Philip Poortmans,Hanneke C. Kluin‐Nelemans,Hanny Haaxma-Reiche,Mars van’t Veer,Mads Hansen,Pierre Soubeyran,Martin Taphoorn,José Thomas,Martin J. van den Bent,M. Fickers,Gustaaf van Imhoff,Cynthia Rozewicz,Ivana Teodorović,M. van Glabbeke
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:21 (24): 4483-4488 被引量:333
标识
DOI:10.1200/jco.2003.03.108
摘要

To confirm the feasibility and estimate the efficacy of methotrexate (MTX), teniposide, carmustine, and methylprednisolone (MBVP) chemotherapy combined with radiotherapy (RT) for patients with non-AIDS-related primary CNS lymphoma (PCNSL) treated in a multicenter setting.Treatment consisted of two cycles of MBVP (MTX 3 g/m2 days 1 and 15, teniposide 100 mg/m2 days 2 and 3, carmustine 100 mg/m2 day 4, methylprednisolone 60 mg/m2 days 1 to 5, and two intrathecal injections of MTX 15 mg, cytarabine 40 mg, and hydrocortisone 25 mg) followed by 40 Gy of RT. Primary end points were response and safety of this regimen.Twelve centers included 52 patients who were all analyzed on an intent-to-treat basis. Median follow-up of all patients was 27 months. One patient progressed and died before treatment, and five patients died during treatment. Four patients received RT after one cycle of chemotherapy, and 42 patients completed the entire treatment. Hematologic grade 3 and 4 toxicity was seen in 78% of patients for leukocytes and 24% of patients for platelets. The overall response rate of all 52 patients was 81%. Two patients who did not fulfill the criteria of objective response survived more than 1 year; one of them is still alive without disease. Eighteen patients died; 11 deaths were a result of tumor, five were probably treatment-related, one was caused by late leukoencephalopathy, and one was a result of intercurrent disease. Median estimated overall survival was 46 months.MBVP followed by RT for PCNSL has a high response rate. However, the 10% toxic death rate during treatment in a multicenter setting underlines the need for highly specialized care.
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