PO.CL01.10 · 临床研究

游离DNA片段组用于转移性结直肠癌患者的治疗反应监测:Dolphin研究

Cell-free DNA fragmentomes for treatment response monitoring in patients with metastatic colorectal cancer: The Dolphin study

海报缩略图:游离DNA片段组用于转移性结直肠癌患者的治疗反应监测:Dolphin研究
编号 5325 展板 20 时间 4/21 09:00–12:00 区域 Section 45 主讲 Denise Steijn, MS
分会场 Liquid Biopsies: Circulating Nucleic Acids 4
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作者与单位 Authors & Affiliations

Denise E. van Steijn1, Lorenzo Rinaldi2, Adria Closa1, Erica Peters2, Alissa Konicki2, Mariska Bierkens1, Haoyue Wang3, Marjolein Greuter3, Birgit Lissenberg-Witte4, Veerle Coupé3, Amoolya Singh2, Timothy McDaniel2, Meike de Wit1, Anna Houben5, Daan van den Broek6, Miriam Koopman5, Gerrit Meijer1, Max Lahaye7, Manon Braat8, Victor Velculescu9, Jeanine Roodhart8, Nicholas Dracopoli2, Frederieke van der Baan6, Geraldine Vink6, Niels Kok10, Remond Fijneman1

1Department of Pathology, Netherlands Cancer Institute, Amsterdam, Netherlands,2DELFI Diagnostics, Baltimore, MD,3Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Amsterdam, Netherlands,4Department of Data Science and Biostatistics, Julius Center for Health Sciences and Primary Care/University Medical Center Utrecht, Utrecht, Netherlands,5Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands,6Department of Laboratory Medicine, Netherlands Cancer Institute, Amsterdam, Netherlands,7Department of Radiology, Netherlands Cancer Institute, Amsterdam, Netherlands,8Department of Radiology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands,9Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD,10Department of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands

摘要 Abstract

中文摘要
引言:对接受全身治疗的转移性结直肠癌(mCRC)患者进行准确的肿瘤反应监测,对于实现及时且明智的治疗决策至关重要。尽管CT成像目前是标准方式,但它存在局限性,包括对检测小病灶的准确性有限以及阅片者间的变异性。可靠的基于血液的生物标志物可能实现对治疗反应更精确和动态的评估。循环肿瘤DNA(ctDNA)能够反映癌细胞负荷,可能补充CT成像来评估治疗反应。DELFI肿瘤分数(DELFI-TF)是一种不依赖突变和肿瘤的ctDNA检测方法,已证明在纵向监测治疗反应方面具有潜力。DOLPHIN研究旨在评估DELFI-TF相对于传统的基于成像的反应监测在mCRC患者中的临床附加价值。 方法:DOLPHIN是前瞻性荷兰结直肠癌队列(Prospective Dutch Colorectal Cancer Cohort)的一项前瞻性观察性子研究,其中在mCRC患者常规CT成像的同时纵向采集血液样本。使用DELFI-TF ctDNA检测方法纵向评估ctDNA水平,该方法是一个锁定并经过验证的机器学习模型,利用来自低覆盖度全基因组测序的游离DNA(cfDNA)片段组数据来定量肿瘤负荷。同时,对肿瘤组织确认存在RAS或BRAF突变的患者样本进行ddPCR分析。本研究的主要终点是ctDNA水平变化与临床确定的治疗反应之间的关联。次要终点包括:ctDNA动态与全身治疗期间多个时间点的临床、生化和影像学反应之间的相关性(I);ctDNA检测相比CT成像识别疾病进展的提前时间(II);纵向ctDNA检测的预后价值(III);以及各种监测方法的成本效益(IV)。 结果:在2023年3月16日至2025年10月16日期间,504例患者在开始二线治疗前被纳入。9例患者因入组标准不符而被排除。患者人口统计学和临床特征的全面概述将在会议上呈现。共采集了2214份血液样本和2468次CT扫描,采集计划将持续到2026年3月。迄今为止,已成功将2186份样本(86.8%)与相应的CT扫描匹配,其中1881份(86.0%)是在成像后14天内获得的。 结论:在正在进行的DOLPHIN研究中,我们成功地将大部分血液样本与相应的CT扫描对齐。本研究将确定DELFI-TF能否补充mCRC患者的治疗反应监测,并可能使部分随访转移到家庭环境中进行。
查看英文原文 English abstract
Introduction: Accurate monitoring of tumor response in patients with metastatic colorectal cancer (mCRC) undergoing systemic therapy is essential to enable timely and informed treatment decisions. Although CT imaging is currently the standard-modality, it has limitations including limited accuracy for detecting small lesions, as well as inter-reader variability. A reliable blood-based biomarker may enable a more precise and dynamic assessment of treatment response. Circulating tumor DNA (ctDNA) is indicative of cancer cell burden and may complement CT imaging for evaluating treatment responses. DELFI tumor fraction (DELFI-TF) is a mutation- and tumor-independent ctDNA assay which has demonstrated potential for longitudinal monitoring of treatment response. The DOLPHIN study aims to evaluate the clinical added value of DELFI-TF to conventional imaging-based response monitoring in patients with mCRC. Method: DOLPHIN is a prospective, observational substudy of the Prospective Dutch Colorectal Cancer Cohort, in which blood samples are collected longitudinally in conjunction with routine CT imaging in mCRC patients. ctDNA levels are longitudinally assessed using the DELFI-TF ctDNA assay, a locked and validated machine learning model that quantifies tumor burden using cell-free DNA (cfDNA) fragmentomic data derived from low-coverage whole genome sequencing. Simultaneously, ddPCR analysis is performed on samples from patients with a tumor tissue-confirmed RAS or BRAF mutation. The primary endpoint of this study is the association between changes in ctDNA levels and clinically determined treatment response. Secondary endpoints include the correlation between ctDNA dynamics and clinical, biochemical, and radiological responses at multiple timepoints during systemic treatment (I), lead time of ctDNA testing compared with CT imaging for identifying progressive disease (II), prognostic value of longitudinal ctDNA testing (III) and the cost-effectiveness of various monitoring approaches (IV). Results: Between March 16 2023 and October 16 2025, 504 patients were enrolled before starting the second line of treatment. Nine patients were excluded due to incorrect entry criteria. A comprehensive overview of patient demographics and clinical characteristics will be presented at the conference. In total 2214 blood samples and 2468 CT scans have been collected, with collection planned to continue until March 2026. To date, 2186 samples (86.8%) have been successfully matched to a corresponding CT scan, and 1881 (86.0%) of these were obtained within 14 days of imaging. Conclusion: In the ongoing DOLPHIN study, we successfully aligned a majority of blood samples with corresponding CT scans. This study will determine whether DELFI-TF can complement treatment response monitoring in mCRC patients and potentially enable parts of follow-up to be shifted to the home setting.
利益披露 Disclosure
D. E. van Steijn, DELFI Diagnostics Other, The first author is employed based on funding by a public private partnership consortium grant in collaboration with Delfi Diagnostics. L. Rinaldi, DELFI Diagnostic Employment, Stock. A. Closa, None. E. Peters, DELFI Diagnostics Employment, Stock. A. Konicki, DELFI Diagnostics Employment, Stock. M. Bierkens, None.. H. Wang, None.. M. Greuter, None.. B. Lissenberg-Witte, None.. V. Coupé, None. A. Singh, DELFI Diagnostics Employment, Stock. T. McDaniel, DELFI Diagnostics Employment, Stock. M. de Wit, None. A. Houben, Amgen, BMS, Delfi Diagnostics, GSK, Incyte, Merck, Natera, Nordic, Personal Genome Diagnostics, Pierre Fabre, Servier ). D. van den Broek, Roche diagnostics Other, Lectures, expert testimony, and advisory board presence. M. Koopman, Eisai, Nordic Pharma, Merck, Pierre Fabre, Servier (transferred to the institute) Other, Advisory role. Bayer, Bristol Myers Squibb, Merck, Personal Genome Diagnostics (PGDx), Pierre Fabre, Roche, Sirtex, Servier ). Servier Other, PI from the international cohort study PROMETCO with Servier as sponsor. G. Meijer, CRCbioscreen BV g., Board of Directors, non-salaried role), Other, Founder. CZ Health Insurances Other, Research collaboration. Sysmex, Sentinel Ch. SpA, Personal Genome Diagnostics (PGDX), Exact Science, DELFi and Hartwig Medical Foundation Patent, Other, Materials, equipment and/or sample/genomic analyses; several patents pending/issued. Dutch Research Council, ZonMw, CZ Health Insurances, PGDX, IKNL, Hartwig Medical Foundation ). CRCbioscreen BV Patent. Health-RI, IKNL, ZonMw, BBMRI-NL, EATRIS-NL g., Board of Directors, non-salaried role). M. Lahaye, None.. M. Braat, None. V. Velculescu, Delfi Diagnostics g., Board of Directors, non-salaried role), Stock, Other, Founder. Johns Hopkins University, Delfi Diagnostics, LabCorp, Qiagen, Sysmex, Agios, Genzyme, Esoterix, Ventana and ManaT Bio Patent. Viron Therapeutics, Epitope Other, Advisor. J. Roodhart, Bayer, BMS, Merck-Serono, Pierre Fabre, Servier, HUB 4 organoids, Cleara Biotech Other, Institutional financial interests. N. Dracopoli, DELFI Diagnostics Employment, Stock. F. van der Baan, Personal Genome Diagnostics Other, Financial support. G. Vink, UMC Utrecht, IKNL Employment. Natera, BMS, Merck, Servier, Personal Genome Diagnostics, Bayer, Sirtex, Nordic Pharma, Pierre Fabre, Lilly, Delfi Diagnostics ). N. Kok, None. R. Fijneman, Delfi Diagnostics, Natera and with Solvias (Cergentis BV), Labcorp (Personal Genome Diagnostics), MERCK BV ), Gift.

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