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米索硝唑与洛莫司汀用于复发性原发性脑肿瘤的化疗

Misonidazole and CCNU chemotherapy for recurrent primary brain tumor.

作者信息

Fulton D S, Urtasun R C, McKinnon S, Tanasichuk H

出版信息

J Neurooncol. 1987;4(4):383-8. doi: 10.1007/BF00195609.

Abstract

CCNU chemotherapy prolongs survival of patients with primary brain tumor when given at the time of tumor progression following radiation therapy. Used as single agent, response rates of 30 to 80 per cent have been reported with median response durations of five to six months. Experimentally, tumor cytotoxicity is enhanced using the combination of misonidazole and CCNU, without increasing myelotoxicity. In this phase I/II study, 23 patients with primary brain tumor which progressed following radiation therapy were treated with combined CCNU and misonidazole. In all patients either the diagnosis of high grade glioma was made at the time of initial diagnosis prior to radiation therapy or the tumor transformed from low grade to high grade glioma at the time of progression following radiation therapy. CCNU 120 mg/M2 was given four hours following misonidazole 3.5 g/M2 every six weeks, with dosage adjustments for myelotoxicity. Treatment was continued for one year or until tumor progression. Of the 17 patients in the study for one year or more, 11 (65 per cent) survived for one year, and six (35 per cent) remained free of tumor progression for one year. Median time to tumor progression from start of CCNU plus misonidazole chemotherapy was 27 weeks and median survival was 80 weeks. No severe complications resulted from myelotoxicity. One patient developed mild peripheral neuropathy which disappeared following discontinuation of misonidazole.

摘要

在放疗后肿瘤进展时给予环磷酰胺(CCNU)化疗可延长原发性脑肿瘤患者的生存期。作为单一药物使用时,据报道缓解率为30%至80%,中位缓解持续时间为5至6个月。在实验中,米索硝唑与CCNU联合使用可增强肿瘤细胞毒性,且不增加骨髓毒性。在这项I/II期研究中,23例放疗后进展的原发性脑肿瘤患者接受了CCNU与米索硝唑联合治疗。所有患者要么在放疗前初始诊断时被诊断为高级别胶质瘤,要么在放疗后进展时肿瘤从低级别转变为高级别胶质瘤。每六周在给予米索硝唑3.5 g/M²后4小时给予CCNU 120 mg/M²,并根据骨髓毒性调整剂量。治疗持续一年或直至肿瘤进展。在该研究中接受治疗一年或更长时间的17例患者中,11例(65%)存活了一年,6例(35%)在一年中无肿瘤进展。从开始CCNU加米索硝唑化疗到肿瘤进展的中位时间为27周,中位生存期为80周。骨髓毒性未导致严重并发症。1例患者出现轻度周围神经病变,在停用米索硝唑后消失。

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