Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures

Author:

Gouda Mohamed A123ORCID,Duose Dzifa Y1,Lapin Morten4,Zalles Stephanie1,Huang Helen J2,Xi Yuanxin5,Zheng Xiaofeng5,Aldesoky Amira I3,Alhanafy Alshimaa M3,Shehata Mohamed A3,Wang Jing5,Kopetz Scott6ORCID,Meric-Bernstam Funda2,Wistuba Ignacio I1,Luthra Rajyalakshmi1,Janku Filip2

Affiliation:

1. Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center , Houston , USA

2. Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center , Houston , USA

3. Department of Clinical Oncology and Nuclear Medicine, Faculty of Medicine, Menoufia University, Shebin Al-Kom , Egypt

4. Department of Hematology and Oncology, Stavanger University Hospital, Stavanger , Norway

5. Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center , Houston , USA

6. Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center , Houston , USA

Abstract

Abstract Detection of methylation patterns in circulating tumor DNA (ctDNA) can offer a novel approach for cancer diagnostics given the unique signature for each tumor type. We developed a next-generation sequencing (NGS)-based assay targeting 32 CpG sites to detect colorectal cancer-specific ctDNA. NGS was performed on bisulfite-converted libraries and status dichotomization was done using median methylation ratios at all targets. We included plasma samples from patients with metastatic colorectal (n = 20) and non-colorectal cancers (n = 8); and healthy volunteers (n = 4). Median methylation ratio was higher in colorectal cancer compared with non-colorectal cancers (P = .001) and normal donors (P = .005). The assay detected ctDNA in 85% of patients with colorectal cancer at a specificity of 92%. Notably, we were able to detect methylated ctDNA in 75% of patients in whom ctDNA was not detected by other methods. Detection of methylated ctDNA was associated with shorter median progression-free survival compared to non-detection (8 weeks versus 54 weeks; P = .027).

Funder

Rising Tide Foundation

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference20 articles.

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3. Methylated circulating tumor DNA as a biomarker in cutaneous melanoma;Diefenbach;Melanoma Manag,2020

4. Epigenetics in cancer;Esteller;N Engl J Med,2008

5. DNA methylation-based testing in liquid biopsies as detection and prognostic biomarkers for the four major cancer types;Constancio;Cells,2020

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