Evidence map›Paper›PMID 42113010›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2026

A Noninvasive Circulating Tumor DNA Methylation Classifier to Identify Benign Pulmonary Nodules.

Qiaomei Guo, Chaoqiang Deng, Xufeng Pan, Jiatao Liu, Guohua Yang, Yuteng Sun, Feng Shi, Mingna Zhao, Xueqing Wang, Shuxuan Yang and 12 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

22 authors.

Qiaomei Guo *Department of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0009-0001-3140-4054
Chaoqiang Deng *Department of Thoracic Surgery and State Key Laboratory of Genetics and Development of Complex Phenotypes, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID 0000-0002-3910-9519
Xufeng Pan *Department of Thoracic Surgery, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0009-0004-1535-1134
Jiatao Liu *Department of Thoracic Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.ORCID 0009-0009-9596-8666
Guohua YangDepartment of Research and Development, Apogenomics Co. Ltd., Shanghai, China.ORCID 0000-0003-3868-3786
Yuteng SunSchool of Laboratory Medicine, Bengbu Medical University, Bengbu, China.ORCID 0009-0000-6979-6236
Feng ShiDepartment of Research and Development, United Imaging Intelligence, Shanghai, China.ORCID 0000-0003-1522-9943
Mingna ZhaoDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0000-0001-8373-7267
Xueqing WangDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0009-0005-3955-3539
Shuxuan YangSchool of Laboratory Medicine, Bengbu Medical University, Bengbu, China.ORCID 0009-0004-4834-3106
Xiaohui LiangDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0009-0007-4742-5056
Wanxing XuDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0009-0000-4669-0121
Jingwen YeDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0009-0009-1214-1111
Xin HuangDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0009-0000-3187-2088
Jiaojiao WuDepartment of Research and Development, United Imaging Intelligence, Shanghai, China.ORCID 0000-0003-2402-7825
Wenyu WangDepartment of Thoracic Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.ORCID 0009-0003-9814-9304
Zhiwei GuoDepartment of Research and Development, Apogenomics Co. Ltd., Shanghai, China.ORCID 0000-0003-4851-0707
Rongjun HuDepartment of Research and Development, Apogenomics Co. Ltd., Shanghai, China.ORCID 0000-0002-4237-8138
Yue YuDepartment of Thoracic Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0001-7457-6596
Yang ZhangDepartment of Thoracic Surgery and State Key Laboratory of Genetics and Development of Complex Phenotypes, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID 0000-0002-9081-0802
Jiatao LouDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0000-0001-8191-3255
Lin WangDepartment of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0000-0002-1787-5298

Funding

National Natural Science Foundation of China (NSFC) 81902453National Natural Science Foundation of China (NSFC) 82273380National Natural Science Foundation of China (NSFC) 82273418National Natural Science Foundation of China (NSFC) 82472375Science and Technology Commission of Shanghai Municipality (STCSM) 22Y11902800Shanghai Rising-Star Program 23QA1407900Shanghai Shen Kang Hospital Development Center SHDC2022CRD020
6 · The paper itself

Abstract

purposeLow-dose computed tomography suffers from a high false-positive rate in the evaluation of pulmonary nodules. Circulating tumor DNA (ctDNA) methylation is a promising complementary biomarker, but its detection is hindered by the highly fragmented nature of ctDNA. EXPERIMENTAL

designWe developed single-strand amplification methylation-targeted sequencing (SAMT-Seq), optimized for methylation detection in fragmented ctDNA. Lung cancer-specific methylation markers were identified from in-house cohort and The Cancer Genome Atlas database and validated in paired tissue and plasma samples from 30 patients with early-stage lung cancer. A panel of 30 key markers was selected using least absolute shrinkage and selection operator (LASSO) regression in a training cohort (n = 239). A Gaussian process classifier was developed and validated in two independent cohorts (n = 59 and n = 207).

resultsSAMT-Seq demonstrated superior analytic sensitivity and on-target efficiency compared with a standard commercial Swift method. The 30-marker classifier yielded area under the curve values of 0.95, 0.95, and 0.92 in the training cohort and validation cohorts 1 and 2, respectively. Notably, it maintained robust performance across nodule types (solid/subsolid), sizes, smoking status, and in situ carcinoma. With a predefined threshold, the model achieved specificity of 100% and 92.16% in validation cohort 1 and 2, respectively, suggesting its potential utility in reducing false-positive classifications.

conclusionsWe developed a high-specificity ctDNA methylation classifier that serves as a practical, complementary tool for risk stratification of pulmonary nodules, with the potential to significantly reduce unnecessary invasive procedures. Ongoing prospective diagnostic validation studies are evaluating its clinical performance.

Indexed as

Biomarkers, TumorCirculating Tumor DNADNA MethylationLung NeoplasmsMultiple Pulmonary NodulesSolitary Pulmonary NoduleAgedFemaleHumansMaleMiddle AgedBiomarkers, TumorCirculating Tumor DNA

Identifiers

PMID42113010
PMCPMC13473858

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.