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复发性多形性胶质母细胞瘤患者的单纯疱疹病毒胸苷激酶/白细胞介素-2联合基因治疗:生物学和临床结果

Combined HSV-TK/IL-2 gene therapy in patients with recurrent glioblastoma multiforme: biological and clinical results.

作者信息

Colombo Federico, Barzon Luisa, Franchin Elisa, Pacenti Monia, Pinna Vittore, Danieli Daniela, Zanusso Mariano, Palù Giorgio

机构信息

Division of Neurosurgery, San Bortolo Hospital, Vicenza, Italy.

出版信息

Cancer Gene Ther. 2005 Oct;12(10):835-48. doi: 10.1038/sj.cgt.7700851.

Abstract

Following our pilot clinical study of combined IL-2/HSV-TK gene therapy for recurrent glioblastoma multiforme (GBM), we extended the protocol to a larger population of patients and evaluated safety, feasibility, and biological activity of treatment. A total of 12 patients received intratumor injection of retroviral vector-producing cells (RVPCs), followed by intravenous ganciclovir (GCV). Treatment was well tolerated with only minor adverse events. Transduction of tumor cells was demonstrated in tumor biopsies. A marked and persistent increase of intratumor and plasma Th1 cytokine levels was demonstrated after RVPC injection. At magnetic resonance imaging evaluation, two patients had a partial response (including a patient showing disappearance of a distant noninjected tumor mass), four had a minor response, four had stable disease, and two had progressive disease. The 6- and 12-month progression-free survival rates were 47 and 14%, respectively. The 6- and 12-month overall survival rates were 58 and 25%, respectively. In conclusion, the results of our clinical protocol of gene therapy for recurrent GBM, based on combined delivery of a suicide and a cytokine gene, demonstrate that intratumor injection of RVPCs was safe, provided effective transduction of the therapeutic genes to target tumor cells, and activated a systemic cytokine cascade, with tumor responses in 50% of cases.

摘要

在我们针对复发性多形性胶质母细胞瘤(GBM)的白细胞介素-2/单纯疱疹病毒胸苷激酶(IL-2/HSV-TK)联合基因治疗的初步临床研究之后,我们将方案扩展至更多患者群体,并评估了治疗的安全性、可行性和生物学活性。共有12例患者接受了肿瘤内注射逆转录病毒载体产生细胞(RVPCs),随后静脉注射更昔洛韦(GCV)。治疗耐受性良好,仅出现轻微不良事件。在肿瘤活检中证实了肿瘤细胞的转导。RVPC注射后,肿瘤内和血浆中Th1细胞因子水平显著且持续升高。在磁共振成像评估中,2例患者有部分缓解(包括1例远处未注射肿瘤肿块消失的患者),4例有轻微缓解,4例病情稳定,2例病情进展。6个月和12个月的无进展生存率分别为47%和14%。6个月和12个月的总生存率分别为58%和25%。总之,我们基于自杀基因和细胞因子基因联合递送的复发性GBM基因治疗临床方案的结果表明,肿瘤内注射RVPCs是安全的,能将治疗基因有效转导至靶肿瘤细胞,并激活全身细胞因子级联反应,50%的病例出现肿瘤反应。

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