Evidence mapPaperPMID 41816417Full record

ArticleJournal of thoracic disease2026

Analysis of clinicopathological characteristics in postoperative molecular residual disease-positive stage I non-small cell lung cancer patients.

Xufeng Deng, Ziqi Huang, Kai Wang, Chengfei Yang, Weikang Shao, Qingyun Li, Jigang Dai, Quanxing Liu

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Article in Journal of thoracic disease, 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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

8 authors.

Xufeng Deng *Department of Thoracic Surgery, The Second Affiliated Hospital, Army Medical University, Chongqing, China.
Ziqi Huang *Department of Thoracic Surgery, The Second Affiliated Hospital, Army Medical University, Chongqing, China.
Kai WangDepartment of Thoracic Surgery, The Second Affiliated Hospital, Army Medical University, Chongqing, China.
Chengfei YangDepartment of Thoracic Surgery, The Second Affiliated Hospital, Army Medical University, Chongqing, China.
Weikang ShaoGenecast Biotechnology Co., Ltd., Wuxi, China.
Qingyun LiGenecast Biotechnology Co., Ltd., Wuxi, China.
Jigang DaiDepartment of Thoracic Surgery, The Second Affiliated Hospital, Army Medical University, Chongqing, China.ORCID https://orcid.org/0000-0002-3699-8138
Quanxing LiuDepartment of Thoracic Surgery, The Second Affiliated Hospital, Army Medical University, Chongqing, China.ORCID https://orcid.org/0000-0002-6725-385X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Multiple primary lung cancers (MPLCs) present unique clinical difficulties because of their genetically diverse independent tumors, requiring genetic testing to distinguish synchronous primaries from intrapulmonary metastases. While circulating tumor DNA (ctDNA) analysis shows potential for detecting molecular residual disease (MRD), tumor heterogeneity hinders its application. Thus, there is an urgent need to develop specific biomarkers and standardize liquid biopsy protocols to improve monitoring and treatment. The aim of this study was to analyze the clinicopathological characteristics of postoperative MRD-positive stage I non-small cell lung cancer (NSCLC) patients, with a focus on the potential utility of ctDNA in detecting MRD and guiding therapeutic decisions. Methods: Twelve patients with pulmonary nodules were analyzed. Paired tissue and plasma samples underwent genomic profiling via next-generation sequencing (NGS) using validated extraction/library preparation kits, following ethical standards. Rigorous quality controls were implemented to ensure sensitive variant detection. Results: Both solitary (n=5) and multiple nodules (n=7) carried Conclusions: Multifocal lung disease exhibits greater genomic complexity and enhanced ctDNA shedding, supporting its use as a disease-tracking tool. The findings identify actionable signatures for MRD surveillance and guide personalized therapeutic interventions based on observed clonal architectures.

Indexed as

biomarkerLung cancer, circulating tumor DNA (ctDNA)molecular residual disease (MRD)next-generation sequencing (NGS)

Identifiers

PMID41816417
PMCPMC12972764

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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 Socratic graph.