癌变·畸变·突变 ›› 2004, Vol. 16 ›› Issue (4): 208-210.doi: 10.3969/j.issn.1004-616x.2004.04.006

• 论著 • 上一篇    下一篇

脑恶性胶质瘤自体瘤苗治疗的临床初步观察

牟永告 ,陈忠平,张湘衡 ,刘然义,李永强   

  1. 中山大学肿瘤防治中心神经外科, 广东 广州 510060
  • 收稿日期:2004-03-31 修回日期:2004-05-10 出版日期:2004-07-30 发布日期:2004-07-30
  • 通讯作者: 牟永告

Preliminary Results of Immunotherapy Against Malignant Gliomas Using Autologous Tumor Cell Vaccine

MU Yong-gao, CHEN Zhong-ping, ZHANG Xiang-heng, et al   

  1. Department of Neurosurgery,Sun Yat-sen University,Guangzhou 510060, China
  • Received:2004-03-31 Revised:2004-05-10 Online:2004-07-30 Published:2004-07-30
  • Contact: MU Yong-gao

摘要: 背景与目的: 探讨NDV(新城鸡瘟病毒)修饰的瘤苗治疗脑恶性胶质瘤的疗效。 材料与方法:自2001-05~2001-11,对8例恶性脑胶质瘤患者给予瘤苗免疫治疗。显微镜下行肿瘤全切除或次全切除,术中留取肿瘤组织备用瘤苗制作和药敏试验;切口愈合后即行放疗;放疗结束后,根据药敏试验结果行化疗一疗程;化疗后4周,行瘤苗治疗,每周注射一次共4次为一疗程。 结果: 通过门诊复查、随访10~25个月。 4例无复发,KPS 90~100分,生存期分别为25、24、20、23个月,平均23个月。复发4例,其中3例死亡,生存期分别为10、14、15个月,1例右额胶质瘤III级者全切除术后13个月复发,行γ刀治疗及化疗,现KPS 90分,已生存19个月,该疗法超过文献中脑恶性胶质瘤中位生存期不足一年的报告。 结论: 恶性脑胶质瘤自体瘤苗治疗理论上可以提高机体的免疫力,预防肿瘤复发,但还需临床和基础的进一步研究,以提高其疗效。

关键词: 胶质瘤, 瘤苗, 免疫治疗

Abstract: BACKGROUND AND AIM: To evaluate the therapeutical effect of autologous Newcastle-Disease-Virus (NDV) modified tumor cell vaccine in the treatment of malignant gliomas. MATERIAL AND METHODS: Eight patients with malignant gliomas were treated with autologous NDV-Modified tumor cell vaccine from May to November of 2001. The tumor was total or sub-total resected under neuromicroscope and the tumor tissues were preserved for vaccine preparation and drug sensitive test. All the patients received postoperative radiotherapy followed by one cycle of chemotherapy. Four weeks after chemotherapy, the patients were immunized with tumor vaccines once a week for four weeks. RESULTS: All the patients were followed up from 10 to 25 months by June of 2003. Four patients survived without the evidence of recurrence with the Karnofsky Performance Scale (KPS) from 90 to 100, and the survival time was 25,24,20 and 23 months, respectively (mean 23 months). Four cases recurred, and three of them died in the 10th, 14th, 15th month after the treatment, respectively. One patient with frontal glioma of Grade III recurred within 13 months after resection. The patient was treated with gamma-knife radiosurgery and chemotherapy and still alive up to 19 months follow-up end.The mean survival time in this therapy was more than one in documents, which was less 1 year for the patients with malignant glionas. CONCLUSIONS: Autologous modified tumor cell vaccines for treatment of malignant gliomas may be a promising alternative to enhance patients' immunity and prevent the recurrence of gliomas, however, its efficiency need to be immproved.

Key words: glioma, vaccination, immunotherapy