Sipos László, Vitanovics Dusan, Afra Dénes
National Institute of Neurosurgery, Budapest.
Ideggyogy Sz. 2004 Nov 20;57(11-12):394-9.
Anaplastic astrocytomas and glioblastomas are the most frequent and most malignant hemispherial tumours. Unfortunately, astrocytic tumours are of infiltrative character and radical removal is not possible. Recurrent malignant gliomas are rarely suitable for reoperation. In most of the cases of recurrent gliomas chemotherapy is the last choice.
Seventy-five consecutive patients with recurrent malignant astrocytomas and glioblastomas had been treated at our institute with per os temozolomide for five days every month. The patients received two to 16 courses of chemotherapy. The toxicity, quality of life, response to chemotherapy and survival data were analysed.
Out of 75 patients four were excluded following the first treatment due to myelotoxicity, and allergic reactions. Among the patients treated with temozolomide in seven cases complete response, 17 partial response, 14 progressive disease were observed. In 33 cases the disease stabilized and out of them in 27% a significant neurological improvement was detected. The time to progression was 6.8 months and the median survival time 8.75 months for patients with glioblastoma and with malignant astrocytoma or malignant mixed oligoastrocytoma 9.45 and 11.15 months, respectively. The overall survival for patients with originally lower grade glioma was 70.32 and for patients with glioblastoma multiforme 17.43 months.
Temozolomide chemotherapy in patients with recurrent malignant astrocytoma and glioblastoma proved to be efficacious and similar good results were achieved as with a nitrosourea based combined chemotherapy. Even in those patients who received previous chemotherapy temozolomide is well tolerated and a relatively long time to progression was achieved in cases of recurrent malignant gliomas. In a few number of patients where BCNU had been previously failed with temozolomide stable disease was achieved. Temozolomide seems to be a promising drug in the chemotherapy of malignant gliomas and can be applied as a second line chemotherapy, as well.
间变性星形细胞瘤和胶质母细胞瘤是最常见且恶性程度最高的半球肿瘤。不幸的是,星形细胞瘤具有浸润性,无法进行根治性切除。复发性恶性胶质瘤很少适合再次手术。在大多数复发性胶质瘤病例中,化疗是最后的选择。
我院连续75例复发性恶性星形细胞瘤和胶质母细胞瘤患者接受了口服替莫唑胺治疗,每月服药5天。患者接受了2至16个疗程的化疗。分析了毒性、生活质量、化疗反应和生存数据。
75例患者中,4例在首次治疗后因骨髓毒性和过敏反应被排除。在接受替莫唑胺治疗的患者中,7例完全缓解,17例部分缓解,14例病情进展。33例病情稳定,其中27%的患者神经功能有显著改善。胶质母细胞瘤患者的疾病进展时间为6.8个月,中位生存时间为8.75个月;恶性星形细胞瘤或恶性混合性少突星形细胞瘤患者的疾病进展时间和中位生存时间分别为9.45个月和11.15个月。原发性低级别胶质瘤患者的总生存时间为70.32个月,多形性胶质母细胞瘤患者为17.43个月。
替莫唑胺化疗在复发性恶性星形细胞瘤和胶质母细胞瘤患者中被证明是有效的,与基于亚硝基脲的联合化疗取得了相似的良好效果。即使是那些之前接受过化疗的患者,替莫唑胺也耐受性良好,复发性恶性胶质瘤患者的疾病进展时间相对较长。在少数之前使用卡莫司汀(BCNU)治疗失败的患者中,使用替莫唑胺后病情稳定。替莫唑胺似乎是恶性胶质瘤化疗中有前景的药物,也可作为二线化疗药物应用。