甲氨蝶呤诱发的一过性脑病。俄罗斯卫生部 N.N. Blokhin 国家肿瘤医学研究中心以俄罗斯医学科学院院士 L.A. Durnov 命名的儿科肿瘤学和血液学研究所的经验

Q4 Medicine
Kh. A. Aleskerova, O. M. Romantsova, V. V. Khairullova, M. M. Efimova, V. Y. Panarina, K. Kirgizov
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引用次数: 0

摘要

简介甲氨蝶呤是抗代谢组的主要化疗药物之一,是骨肉瘤的一线治疗药物。根据EURAMOS-1方案,该药物的使用剂量为12克/平方米。甲氨蝶呤引起的并发症包括肾毒性、肝毒性、骨髓抑制、皮肤和粘膜溃疡、消化不良。其中一种可怕但可逆的并发症是甲氨蝶呤诱发的一过性脑病(MIE),在使用大剂量甲氨蝶呤(HD MTX)治疗的患者中,15%以上会出现这种临床表现。俄罗斯卫生部 N.N. Blokhin 国家肿瘤医学研究中心以俄罗斯医学科学院院士 L.A. Durnov 命名的儿科肿瘤学和血液学研究所在 2013 年至 2023 年期间记录了 10 例 MIE。所有患者均按照 EURAMOS-1 方案接受治疗。10例患者中有4例在化疗后出现HD MTX消除延迟。没有一名患者在使用 HD MTX 时出现电解质紊乱。并发症出现的中位时间为 7 天(从开始治疗的 5 天到 10 天不等),最常见的并发症是在使用 12 克/平方米甲氨蝶呤的 3 个疗程后出现的,这相当于总共使用了 6 个剂量的甲氨蝶呤。神经系统症状:头痛、视力障碍、失语、抽搐均为一过性症状,平均在治疗开始 24 小时后缓解。所有 10 名患者都接受了强制性碱化、大量输液治疗、神经保护药物以及减充血剂治疗,以治疗 MIE。随后,10 名患者中有 9 人继续接受甲氨蝶呤治疗。目前还没有治疗 MIE 的标准建议。然而,出现严重的神经毒性并不排除在治疗方案中继续使用 HD MTX 的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methotrexate-induced transient encephalopathy. The experience of the Research Institute of Pediatric Oncology and Hematology named after Academician of the Russian Academy of Medical Sciences L.A. Durnov at N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Introduction. Methotrexate is one of the main chemotherapeutic agents of group antimetabolits, includes in the first line of therapy against osteosarcoma. The drug uses in dose 12 g/m2 according to the protocol EURAMOS-1. The range of methotrexate-induced complications includes renal toxity, hepatotoxicity, myelosuppression, skin and mucosal ulcerations, dyspeptic disorders. One of the formidable, but reversible complications, is methotrexate-induced transient encephalopathy (MIE), the clinical manifestations of which occur in more than 15 % of patients in the treatment of which high doses of methotrexate (HD MTX) are used.Materials and methods. At the Research Institute of Pediatric Oncology and Hematology named after Academician of the Russian Academy of Medical Sciences L.A. Durnov at N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia the period from 2013 to 2023 10 cases of MIE were recorded. All patients received therapy according to the protocol EURAMOS-1. The 4 out of 10 patients had a delay in the rate of elimination of HD MTX after the course of chemotherapy. No one patient had electrolyte disturbances with using HD MTX. The median occurrence of the complication’s emerging was 7 days (from 5 to 10 from the start of therapy) and most often developed after 3 courses of methotrexate 12 g/m2 , which corresponds in total 6 doses of methotrexate. Neurological symptoms: headache, visual impairment, aphasia, convulsions were transient and resolved after an average of 24 hours from the start of the treatment.Results. All 10 patients received obligatory alkalization, massive infusion therapy, neuroprotective drugs, as well as decongestant therapy as a treatment of MIE. Subsequently, therapy with methotrexate was continued for the 9 of 10 patients.Conclusions. The standard recommendations for the treatment of MIE do not currently exist. However, the development of severe neurotoxicity does not exclude the possibility of further using of HD MTX in the treatment program
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来源期刊
Russian Journal of Pediatric Hematology and Oncology
Russian Journal of Pediatric Hematology and Oncology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
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