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Clinical Utility of Tumor-Naive Presurgical Circulating Tumor DNA Detection in Early-Stage NSCLC

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dc.contributor.author홍태희-
dc.date.accessioned2025-02-03T08:02:48Z-
dc.date.available2025-02-03T08:02:48Z-
dc.date.issued2024-11-
dc.identifier.issn1556-0864-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/201531-
dc.description.abstractObjectives: The use of tumor-informed circulating tumor DNA (ctDNA) testing in patients with early-stage disease before surgery is limited, mainly owing to restricted tissue access and extended turnaround times. This study aimed to evaluate the clinical value of a tumor-naïve, methylation-based cell-free DNA assay in a large cohort of patients with resected NSCLC. Method: We analyzed presurgical plasma samples from 895 patients with EGFR and anaplastic lymphoma kinase-wild-type, clinical stage I or II NSCLC. The ctDNA status was evaluated for its prognostic significance in relation to tumor volume, metabolic activity, histologic diagnosis, histologic subtypes, and clinical-to-pathologic TNM upstaging. Results: Presurgical ctDNA detection was observed in 55 of 414 patients (13%) with clinical stage I lung adenocarcinoma (LUAD) and was associated with poor recurrence-free survival (2-year recurrence-free survival 69% versus 91%; log-rank p < 0.001), approaching that of clinical stage II LUAD. Presurgical ctDNA detection was not prognostic in patients with clinical stage II LUAD or non-LUAD. Within LUAD, tumor volume and positron emission tomography avidity interacted to predict presurgical ctDNA detection. Moreover, presurgical ctDNA detection was predictive of the postsurgical discovery of International Association for the Study of Lung Cancer grade 3 tumors (p < 0.001) and pathologic TNM upstaging (p < 0.001). Notably, presurgical ctDNA detection strongly correlated with higher programmed death-ligand 1 expression in tumors (positive rates 28% versus 55%, p < 0.001), identifying a subgroup likely to benefit from anti-programmed death-ligand 1 therapies. Conclusion: These findings support the integration of ctDNA testing into routine diagnostic workflows in early-stage NSCLC without the need for tumor tissue profiling. Furthermore, it is clinically useful in identifying patients at high risk who might benefit from innovative treatments, including neoadjuvant immune checkpoint inhibitors.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfJOURNAL OF THORACIC ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBiomarkers, Tumor / blood-
dc.subject.MESHBiomarkers, Tumor / genetics-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / blood-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / genetics-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / pathology-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / surgery-
dc.subject.MESHCirculating Tumor DNA* / blood-
dc.subject.MESHCirculating Tumor DNA* / genetics-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLung Neoplasms* / blood-
dc.subject.MESHLung Neoplasms* / genetics-
dc.subject.MESHLung Neoplasms* / pathology-
dc.subject.MESHLung Neoplasms* / surgery-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Staging*-
dc.subject.MESHPrognosis-
dc.titleClinical Utility of Tumor-Naive Presurgical Circulating Tumor DNA Detection in Early-Stage NSCLC-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Thoracic and Cardiovascular Surgery (흉부외과학교실)-
dc.contributor.googleauthorTae Hee Hong-
dc.contributor.googleauthorSoohyun Hwang-
dc.contributor.googleauthorAbhijit Dasgupta-
dc.contributor.googleauthorChris Abbosh-
dc.contributor.googleauthorTiffany Hung-
dc.contributor.googleauthorJörg Bredno-
dc.contributor.googleauthorJill Walker-
dc.contributor.googleauthorXiaojin Shi-
dc.contributor.googleauthorTsveta Milenkova-
dc.contributor.googleauthorLeora Horn-
dc.contributor.googleauthorJoon Young Choi-
dc.contributor.googleauthorHo Yun Lee-
dc.contributor.googleauthorJong Ho Cho-
dc.contributor.googleauthorYong Soo Choi-
dc.contributor.googleauthorYoung Mog Shim-
dc.contributor.googleauthorShoujie Chai-
dc.contributor.googleauthorKate Rhodes-
dc.contributor.googleauthorManami Roychowdhury-Saha-
dc.contributor.googleauthorDarren Hodgson-
dc.contributor.googleauthorHong Kwan Kim-
dc.contributor.googleauthorMyung-Ju Ahn-
dc.identifier.doi10.1016/j.jtho.2024.07.002-
dc.contributor.localIdA06574-
dc.relation.journalcodeJ01909-
dc.identifier.eissn1556-1380-
dc.identifier.pmid38992468-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S155608642400666X-
dc.subject.keywordCancer detection-
dc.subject.keywordCell-free DNA-
dc.subject.keywordNSCLC-
dc.subject.keywordRecurrence-
dc.subject.keywordStaging-
dc.contributor.alternativeNameHong, Tae Hee-
dc.contributor.affiliatedAuthor홍태희-
dc.citation.volume19-
dc.citation.number11-
dc.citation.startPage1512-
dc.citation.endPage1524-
dc.identifier.bibliographicCitationJOURNAL OF THORACIC ONCOLOGY, Vol.19(11) : 1512-1524, 2024-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Thoracic and Cardiovascular Surgery (흉부외과학교실) > 1. Journal Papers

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