VOLTAGE-2: multicenter phase II study of nivolumab monotherapy in patients with mismatch repair-deficient resectable locally advanced rectal cancer

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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Abstract

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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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
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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