Accurate Early Detection and EGFR Mutation Status Prediction of Lung Cancer Using Plasma cfDNA Coverage Patterns: A Proof-of-Concept Study

Author:

Bie Zhixin1,Ping Yi2ORCID,Li Xiaoguang1,Lan Xun2345,Wang Lihui2

Affiliation:

1. Department of Minimally Invasive Tumor Therapies Center, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, No. 1 Dongdan Dahua Street, Beijing 100730, China

2. Department of Basic Medical Sciences, School of Medicine, Tsinghua University, Beijing 100084, China

3. Tsinghua-Peking Joint Center for Life Sciences, Tsinghua University, Beijing 100084, China

4. Centre for Life Sciences, Tsinghua University, Beijing 100084, China

5. MOE Key Laboratory of Bioinformatics, Tsinghua University, Beijing 100084, China

Abstract

Lung cancer is a major global health concern with a low survival rate, often due to late-stage diagnosis. Liquid biopsy offers a non-invasive approach to cancer detection and monitoring, utilizing various features of circulating cell-free DNA (cfDNA). In this study, we established two models based on cfDNA coverage patterns at the transcription start sites (TSSs) from 6X whole-genome sequencing: an Early Cancer Screening Model and an EGFR mutation status prediction model. The Early Cancer Screening Model showed encouraging prediction ability, especially for early-stage lung cancer. The EGFR mutation status prediction model exhibited high accuracy in distinguishing between EGFR-positive and wild-type cases. Additionally, cfDNA coverage patterns at TSSs also reflect gene expression patterns at the pathway level in lung cancer patients. These findings demonstrate the potential applications of cfDNA coverage patterns at TSSs in early cancer screening and in cancer subtyping.

Publisher

MDPI AG

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