VOLTAGE-2:针对错配修复缺陷可切除局部晚期直肠癌患者的 nivolumab 单药治疗多中心 II 期研究

H. Bando , Y. Tsukada , S. Kumagai , Y. Miyashita , A. Taketomi , S. Yuki , Y. Komatsu , T. Akiyoshi , E. Shinozaki , Y. Kanemitsu , A. Takashima , M. Shiozawa , A. Shiomi , K. Yamazaki , N. Matsuhashi , H. Hasegawa , T. Kato , E. Oki , M. Fukui , M. Wakabayashi , T. Yoshino
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引用次数: 0

摘要

背景新辅助放疗和化疗,然后进行手术切除,是局部晚期直肠癌(LARC)的标准治疗方法。新的证据显示,抗程序性细胞死亡蛋白1(anti-PD-1)疗法对错配修复缺陷(dMMR)结直肠癌患者有疗效,尤其是在控制转移性疾病方面。患者和方法在此,我们介绍 VOLTAGE-2 研究(EPOC 2201),这是一项非随机、单臂、II 期试验,旨在研究 nivolumab 单药治疗 dMMR 可切除 LARC 患者一年的疗效和安全性。临床完全应答(cCR)或接近完全应答(nCR)的患者将采用纪念斯隆-凯特琳回归方案进行非手术治疗(NOM)观察。主要终点是研究者确定的nivolumab单药治疗2年的cCR率。我们将使用基于全基因组测序(WGS)的分子残留疾病(MRD)检测方法研究循环肿瘤DNA检测作为cCR的替代性,并将使用全外显子组测序(WES)和基于全转录组测序(WTS)的肿瘤基因组学和免疫微环境评估方法评估抗PD-1抗体反应的生物标志物。我们计划利用人工智能和深度学习驱动的基因组学、转录组学、放射组学、病理组学、结肠镜成像、生活质量和临床特征进行时空跨组学分析。
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VOLTAGE-2: multicenter phase II study of nivolumab monotherapy in patients with mismatch repair-deficient resectable locally advanced rectal cancer

Background

Neoadjuvant radiotherapy and chemotherapy, followed by surgical resection, are standard treatments for locally advanced rectal cancer (LARC). Emerging evidence has shown the efficacy of anti-programmed cell death protein 1 (anti-PD-1) therapy for patients with mismatch repair-deficient (dMMR) colorectal cancer, particularly in managing metastatic disease. Several ongoing clinical trials evaluating the efficacy of anti-PD-1 therapy in patients with dMMR LARC have reported outstanding responses.

Patients and methods

Here, we present the VOLTAGE-2 study (EPOC 2201), a non-randomized, single-arm, phase II trial that aims to investigate the efficacy and safety of nivolumab monotherapy for 1 year in patients with dMMR-resectable LARC. Patients with clinical complete response (cCR) or near-complete response (nCR) will be observed with non-operative management (NOM) using the Memorial Sloan Kettering Regression Schema.

The primary endpoint will be investigator-determined 2-year cCR rate for nivolumab monotherapy. We will investigate the surrogacy of circulating tumor DNA assay as a cCR using whole-genome sequencing (WGS)-based molecular residual disease (MRD) assay and will evaluate the biomarkers of the response to anti-PD-1 antibody using whole-exome sequencing (WES) plus whole-transcriptome sequencing (WTS)-based tumor genomics and immune microenvironment evaluations. We plan to carry out spatiotemporal trans-omics analyses using artificial intelligence and deep learning-driven genomics, transcriptomics, radiomics, pathomics, colonoscopic imaging, quality of life, and clinical features.

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