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射频消融联合肽新抗原疫苗接种:未来癌症免疫治疗的有前途模式。

Combination treatment of radiofrequency ablation and peptide neoantigen vaccination: Promising modality for future cancer immunotherapy.

机构信息

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Hangzhou Neoantigen Therapeutics Co., Ltd., Hangzhou, China.

出版信息

Front Immunol. 2022 Sep 29;13:1000681. doi: 10.3389/fimmu.2022.1000681. eCollection 2022.

Abstract

BACKGROUND

The safety and immunogenicity of a personalized neoantigen-based peptide vaccine, iNeo-Vac-P01, was reported previously in patients with a variety of cancer types. The current study investigated the synergistic effects of radiofrequency ablation (RFA) and neoantigen vaccination in cancer patients and tumor-bearing mice.

METHODS

Twenty-eight cancer patients were enrolled in this study, including 10 patients who had received RFA treatment within 6 months before vaccination (Cohort 1), and 18 patients who had not (Cohort 2). Individualized neoantigen peptide vaccines were designed, manufactured, and subcutaneously administrated with GM-CSF as an adjuvant for all patients. Mouse models were employed to validate the synergistic efficacy of combination treatment of RFA and neoantigen vaccination.

RESULTS

Longer median progression free survival (mPFS) and median overall survival (mOS) were observed in patients in Cohort 1 compared to patients in Cohort 2 (4.42 and 20.18 months vs. 2.82 and 10.94 months). The results of IFN-γ ELISpot assay showed that patients in Cohort 1 had stronger neoantigen-specific immune responses at baseline and post vaccination. Mice receiving combination treatment of RFA and neoantigen vaccines displayed higher antitumor immune responses than mice receiving single modality. The combination of PD-1 blockage with RFA and neoantigen vaccines further enhanced the antitumor response in mice.

CONCLUSION

Neoantigen vaccination after local RFA treatment could improve the clinical and immune response among patients of different cancer types. The synergistic antitumor potentials of these two modalities were also validated in mice, and might be further enhanced by immune checkpoint inhibition. The mechanisms of their synergies require further investigation.

CLINICAL TRIAL REGISTRATION

https://clinicaltrials.gov/, identifier NCT03662815.

摘要

背景

先前有研究报道了一种基于个体化新生抗原的肽疫苗 iNeo-Vac-P01 在多种癌症类型患者中的安全性和免疫原性。本研究旨在探究射频消融(RFA)与新生抗原疫苗接种联合应用于癌症患者及荷瘤小鼠的协同作用。

方法

本研究共纳入 28 例癌症患者,其中 10 例患者在接种疫苗前 6 个月内接受了 RFA 治疗(队列 1),18 例患者未接受 RFA 治疗(队列 2)。所有患者均接受了个体化新生抗原肽疫苗接种,疫苗联合 GM-CSF 作为佐剂进行皮内注射。同时构建了小鼠模型,以验证 RFA 和新生抗原疫苗联合治疗的协同疗效。

结果

队列 1 患者的中位无进展生存期(mPFS)和中位总生存期(mOS)均长于队列 2 患者(4.42 个月和 20.18 个月 vs. 2.82 个月和 10.94 个月)。IFN-γ ELISpot 检测结果显示,队列 1 患者在基线和接种疫苗后的新生抗原特异性免疫反应更强。与接受单一治疗的小鼠相比,接受 RFA 和新生抗原疫苗联合治疗的小鼠表现出更强的抗肿瘤免疫反应。此外,PD-1 阻断联合 RFA 和新生抗原疫苗进一步增强了小鼠的抗肿瘤反应。

结论

局部 RFA 治疗后进行新生抗原疫苗接种可以改善不同癌症类型患者的临床和免疫反应。在小鼠模型中也验证了这两种治疗方式的协同抗肿瘤潜力,并且免疫检查点抑制可能进一步增强其抗肿瘤作用。其协同作用的机制需要进一步研究。

临床试验注册

https://clinicaltrials.gov/,标识符 NCT03662815。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc38/9559398/7bdde0c0bfc7/fimmu-13-1000681-g001.jpg

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