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首页> 外文期刊>Journal of Translational Medicine >A pilot clinical trial testing mutant von Hippel-Lindau peptide as a novel immune therapy in metastatic Renal Cell Carcinoma
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A pilot clinical trial testing mutant von Hippel-Lindau peptide as a novel immune therapy in metastatic Renal Cell Carcinoma

机译:一项试验性临床试验测试了突变型von Hippel-Lindau肽作为转移性肾细胞癌的新型免疫疗法

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Background Due to the lack of specific tumor antigens, the majority of tested cancer vaccines for renal cell carcinoma (RCC) are based on tumor cell lysate. The identification of the von Hippel-Lindau (VHL) gene mutations in RCC patients provided the potential for developing a novel targeted vaccine for RCC. In this pilot study, we tested the feasibility of vaccinating advanced RCC patients with the corresponding mutant VHL peptides. Methods Six patients with advanced RCC and mutated VHL genes were vaccinated with the relevant VHL peptides. Patients were injected with the peptide mixed with Montanide subcutaneously (SQ) every 4 weeks until disease progression or until the utilization of all available peptide stock. Results Four out of five evaluable patients (80%) generated specific immune responses against the corresponding mutant VHL peptides. The vaccine was well tolerated. No grade III or IV toxicities occurred. The median overall survival (OS) and median progression-free survival (PFS) were 30.5 and 6.5 months, respectively. Conclusions The vaccine demonstrated safety and proved efficacy in generating specific immune response to the mutant VHL peptide. Despite the fact that the preparation of these custom-made vaccines is time consuming, the utilization of VHL as a vaccine target presents a promising approach because of the lack of other specific targets for RCC. Accordingly, developing mutant VHL peptides as vaccines for RCC warrants further investigation in larger trials. Trial registration: 98C0139
机译:背景技术由于缺乏特异性肿瘤抗原,大多数用于肾细胞癌(RCC)的测试癌症疫苗均基于肿瘤细胞裂解液。对RCC患者中的von Hippel-Lindau(VHL)基因突变的鉴定为开发针对RCC的新型靶向疫苗提供了潜力。在这项初步研究中,我们测试了用相应的突变VHL肽为晚期RCC患者接种疫苗的可行性。方法对6例晚期RCC和VHL基因突变的患者接种相关的VHL肽。每4周向患者皮下注射与Montanide混合的肽,直至疾病进展或直至利用所有可用的肽储备。结果五分之四的可评估患者(80%)产生了针对相应突变型VHL肽的特异性免疫反应。疫苗耐受良好。没有发生III级或IV级毒性。中位总体生存期(OS)和无进展生存期(PFS)分别为30.5和6.5个月。结论该疫苗证明了安全性,并证明了对突变VHL肽产生特异性免疫应答的功效。尽管制备这些定制疫苗是耗时的事实,但由于缺乏RCC的其他特定靶标,将VHL用作疫苗靶标还是一种有前途的方法。因此,开发突变的VHL肽作为RCC疫苗值得在更大的试验中进一步研究。试用注册:98C0139

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