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A Phase Ib Trial of Personalized Neoantigen Therapy Plus Anti-PD-1 in Patients with Advanced Melanoma, Non-small Cell Lung Cancer, or Bladder Cancer

机译:个性化新洲治疗的A相IB试验加上先进黑素瘤,非小细胞肺癌或膀胱癌患者的抗PD-1

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摘要

Neoantigens arise from mutations in cancer cells and are important targets of T cell-mediated anti-tumor immunity. Here, we report the first open-label, phase lb clinical trial of a personalized neoantigen-based vaccine, NEO-PV-01, in combination with PD-1 blockade in patients with advanced melanoma, non-small cell lung cancer, or bladder cancer. This analysis of 82 patients demonstrated that the regimen was safe, with no treatment-related serious adverse events observed. De novo neoantigen-specific CD4(+) and CD8(+) T cell responses were observed post-vaccination in all of the patients. The vaccine-induced T cells had a cytotoxic phenotype and were capable of trafficking to the tumor and mediating cell killing. In addition, epitope spread to neoantigens not included in the vaccine was detected post-vaccination. These data support the safety and immunogenicity of this regimen in patients with advanced solid tumors.
机译:新抗原源于癌细胞的突变,是T细胞介导的抗肿瘤免疫的重要靶点。在此,我们报告了个性化新抗原疫苗NEO-PV-01与PD-1阻断剂联合应用于晚期黑色素瘤、非小细胞肺癌或膀胱癌患者的首次开放标签、lb期临床试验。对82名患者的分析表明,该方案是安全的,没有观察到与治疗相关的严重不良事件。所有患者接种疫苗后均观察到新抗原特异性CD4(+)和CD8(+)T细胞反应。疫苗诱导的T细胞具有细胞毒性表型,能够转运至肿瘤并介导细胞杀伤。此外,疫苗接种后检测到表位扩散到疫苗中未包含的新抗原。这些数据支持该方案在晚期实体瘤患者中的安全性和免疫原性。

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