Colombo Federico, Barzon Luisa, Franchin Elisa, Pacenti Monia, Pinna Vittore, Danieli Daniela, Zanusso Mariano, Palù Giorgio
Division of Neurosurgery, San Bortolo Hospital, Vicenza, Italy.
Cancer Gene Ther. 2005 Oct;12(10):835-48. doi: 10.1038/sj.cgt.7700851.
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.
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。