PO.CL01.06 · 临床研究

基线DKK1血浆水平升高是sirexatamab治疗的结直肠癌患者的生物标志物

Elevated baseline DKK1 plasma is a biomarker for sirexatamab treated colorectal cancer patients

海报缩略图:基线DKK1血浆水平升高是sirexatamab治疗的结直肠癌患者的生物标志物
编号 7715 展板 6 时间 4/22 09:00–12:00 区域 Section 41 主讲 Michael Kagey, PhD
分会场 Biomarkers Predictive of Therapeutic Benefit 6
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作者与单位 Authors & Affiliations

Zongzhong Tong1, Scott Patton1, Patty Ormonde-Hanson1, Calvin Jia2, Cyndi Sirard2, Jay Baum2, Mike Kagey2

1ARUP Laboratories, Salt Lake City, UT,2Leap Therapeutics, Cambridge, MA

摘要 Abstract

中文摘要
Sirexatamab是一种IgG4单克隆抗体,可强效中和dickkopf相关蛋白1(DKK1)。DKK1是一种分泌型蛋白,已被认为是结直肠癌(CRC)的不良预后标志物和致癌驱动因子。DeFianCe(NCT05480306)研究是一项2期随机、全球、开放标签、多中心研究,旨在评估sirexatamab联合当前标准治疗(SOC)方案(FOLFIRI/FOLFOX和贝伐珠单抗)相比SOC作为晚期CRC参与者二线治疗的疗效和安全性(n=188)。使用一种研究性检测方法对基线血浆DKK1水平进行的回顾性分析发现,在DKK1水平升高的患者中,实验组的无进展生存期和总生存期得到显著改善。为了支持未来的前瞻性患者筛选,开发了一种使用Meso Scale Discovery(MSD)平台的优化DKK1检测方法,并在中心实验室进行了可行性验证。使用优化后的检测方法对DeFianCe样本进行了重新检测。与研究性检测方法一致,DKK1水平高于中位数的患者在实验组中相比SOC显示出改善的临床结局。此外,评估了约500份商业CRC血浆样本,以确定真实世界数据集中DKK1升高患者的流行率,并了解人口统计学特征与DKK1水平之间的关联。未来工作将包括完成该检测方法作为潜在伴随诊断的开发和验证,并确定最有可能从基于sirexatamab疗法中获得临床获益的CRC患者的适宜DKK1血浆水平阈值。
查看英文原文 English abstract
Sirexatamab is an IgG4 monoclonal antibody that potently neutralizes dickkopf-related protein 1 (DKK1). DKK1 is a secreted protein that has been implicated as a poor prognostic marker and as an oncogenic driver for colorectal cancer (CRC). The DeFianCe (NCT05480306) Phase 2 randomized, global, open-label, multicenter study was conducted to evaluate the efficacy and safety of sirexatamab plus the current standard of care (SOC) treatment regimen (FOLFIRI/FOLFOX and bevacizumab) versus SOC as second-line treatment for participants with advanced CRC (n=188). A retrospective analysis of baseline plasma levels of DKK1 using a research assay identified a significant improvement in progression free and overall survival favoring the experimental arm in patients with elevated levels of DKK1. In order to enable future prospective patient selection, an optimized DKK1 assay using the Meso Scale Discovery (MSD) platform was developed and underwent feasibility at a central laboratory. DeFianCe samples were retested with the optimized assay. Consistent with the research assay, patients whose DKK1 levels were above the median showed improved clinical outcomes in the experimental arm compared to SOC. Furthermore, approximately 500 commercial CRC plasma samples were evaluated to determine the prevalence of patients with elevated DKK1 in a real-world data set and understand the association between demographics and DKK1 levels. Future work will include completing the development and validation of the assay as a potential companion diagnostic and determining the appropriate threshold of DKK1 plasma levels for CRC patients who would be most likely to derive clinical benefit from a sirexatamab-based therapy.
利益披露 Disclosure
Z. Tong, ARUP Laboratories Employment. S. Patton, ARUP Laboratories Employment. P. Ormonde-Hanson, ARUP Laboratories Employment. C. Jia, Leap Therapeutics Employment, Stock Option. C. Sirard, Leap Therapeutics Employment, Stock Option. J. Baum, Leap Therapeutics Employment, Stock Option. M. Kagey, Leap Therapeutics Employment, Stock Option.

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