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采用化疗和抗 PD-1 药物联合治疗作为一线治疗方案,为非鳞状非小细胞肺癌患者接种个体化新抗原疫苗 NEO-PV-01。

Personalized neoantigen vaccine NEO-PV-01 with chemotherapy and anti-PD-1 as first-line treatment for non-squamous non-small cell lung cancer.

机构信息

Dana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Cancer Cell. 2022 Sep 12;40(9):1010-1026.e11. doi: 10.1016/j.ccell.2022.08.003. Epub 2022 Aug 25.

Abstract

Neoantigens arising from mutations in tumor DNA provide targets for immune-based therapy. Here, we report the clinical and immune data from a Phase Ib clinical trial of a personalized neoantigen-vaccine NEO-PV-01 in combination with pemetrexed, carboplatin, and pembrolizumab as first-line therapy for advanced non-squamous non-small cell lung cancer (NSCLC). This analysis of 38 patients treated with the regimen demonstrated no treatment-related serious adverse events. Multiple parameters including baseline tumor immune infiltration and on-treatment circulating tumor DNA levels were highly correlated with clinical response. De novo neoantigen-specific CD4 and CD8 T cell responses were observed post-vaccination. Epitope spread to non-vaccinating neoantigens, including responses to KRAS G12C and G12V mutations, were detected post-vaccination. Neoantigen-specific CD4 T cells generated post-vaccination revealed effector and cytotoxic phenotypes with increased CD4 T cell infiltration in the post-vaccine tumor biopsy. Collectively, these data support the safety and immunogenicity of this regimen in advanced non-squamous NSCLC.

摘要

肿瘤 DNA 突变产生的新抗原为免疫治疗提供了靶点。在这里,我们报告了一项 I 期临床试验的临床和免疫数据,该试验将个体化新抗原疫苗 NEO-PV-01 与培美曲塞、卡铂和帕博利珠单抗联合用于晚期非鳞状非小细胞肺癌 (NSCLC) 的一线治疗。对 38 例接受该方案治疗的患者的分析表明,没有与治疗相关的严重不良事件。包括基线肿瘤免疫浸润和治疗期间循环肿瘤 DNA 水平在内的多个参数与临床反应高度相关。接种疫苗后可观察到新抗原特异性 CD4 和 CD8 T 细胞反应。接种疫苗后还检测到抗原表位扩展到非疫苗新抗原,包括对 KRAS G12C 和 G12V 突变的反应。接种疫苗后产生的新抗原特异性 CD4 T 细胞表现出效应和细胞毒性表型,在接种疫苗后的肿瘤活检中 CD4 T 细胞浸润增加。总的来说,这些数据支持该方案在晚期非鳞状 NSCLC 中的安全性和免疫原性。

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