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使用阿霉素、VM 26和洛莫司汀联合治疗成人恶性胶质瘤和脑转移瘤。II期试验结果

Treatment of malignant gliomas and brain metastases in adults using a combination of adriamycine, VM 26, and CCNU. Results of a type II trial.

作者信息

Pouillart P, Mathé G, Palangie T, Lheritier J, Poisson M, Huguenin P, Gautier H, Morin P, Parrot R

出版信息

Recent Results Cancer Res. 1977(62):17-28. doi: 10.1007/978-3-642-81174-6_5.

Abstract

Forty-three patients with inoperable and/or recurring malignant gliomas and 30 patients with multiple recurring brain metastases were treated with a combination of adriamycine (45 mg/m 2 and 4-dimethyl-epipodophyllotoxin D-thenylidene (VM 26) (60 mg/m 2 for 2 days) and 1-(2-chloroethyl)-3-cyclohexyl-1-nitroso-urea (CCNU) (60 mg/m 2 for 2 days). These cycles of treatment were repeated as soon as the hematologic restoration was complete. The treatment was well-tolerated and the clinical condition of 31 out of 43 glioblastoma patients improved during the 2 months after the beginning of the treatment. Six out of eight patients with breast cancer metastases, one out of 13 with bronchial cancer metastases, and three out of nine with other types of cancer metastases also benefitted from the treatment. Examination of the results reveals the following characteristics: 1. A low degree of efficiency of this combination in the treatment of brain metastases, except for breast cancer metastases. 2. Absence of complete correlation between the clinical results observed and the cinegammagraphic developments 3. Similarity of the results independent of the initial localization 4. Establishment of a 6-month median survival period, with ten patients at present in a state of apparently complete remission, 180-506 days after beginning of the treatment.

摘要

43例无法手术切除和/或复发性恶性胶质瘤患者以及30例多发性复发性脑转移瘤患者接受了阿霉素(45mg/m²)、4-二甲基表鬼臼噻吩糖苷(VM26)(60mg/m²,连用2天)和1-(2-氯乙基)-3-环己基-1-亚硝基脲(CCNU)(60mg/m²,连用2天)联合治疗。一旦血液学指标恢复正常,就重复进行这些治疗周期。该治疗耐受性良好,43例胶质母细胞瘤患者中有31例在治疗开始后的2个月内临床状况有所改善。8例乳腺癌脑转移患者中有6例、13例支气管癌脑转移患者中有1例以及9例其他类型癌脑转移患者中有3例也从该治疗中获益。对结果的检查显示出以下特点:1. 除乳腺癌脑转移外,该联合治疗对脑转移瘤的治疗效率较低。2. 观察到的临床结果与闪烁γ照相术进展之间不存在完全相关性。3. 结果与初始定位无关。4. 确定了6个月的中位生存期,目前有10例患者处于明显完全缓解状态,治疗开始后180 - 506天。

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