12 39

Cited 2 times in

Cited 0 times in

Prognostic Value of Residual Circulating Tumor DNA in Metastatic Pancreatic Ductal Adenocarcinoma

DC Field Value Language
dc.contributor.authorKim, Hongkyung-
dc.contributor.authorLee, Jinho-
dc.contributor.authorPark, Mi Ri-
dc.contributor.authorChoi, Zisun-
dc.contributor.authorHan, Seung Jung-
dc.contributor.authorKim, Dongha-
dc.contributor.authorShin, Saeam-
dc.contributor.authorLee, Seung-Tae-
dc.contributor.authorChoi, Jong Rak-
dc.contributor.authorPark, Seung Woo-
dc.date.accessioned2025-11-14T02:01:41Z-
dc.date.available2025-11-14T02:01:41Z-
dc.date.created2025-07-29-
dc.date.issued2025-03-
dc.identifier.issn2234-3806-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/208825-
dc.description.abstractBackground: Circulating tumor DNA (ctDNA) is a potential biomarker in pancreatic ductal adenocarcinoma (PDAC). However, studies on residual ctDNA in patients post-chemotherapy are limited. We assessed the prognostic value of residual ctDNA in metastatic PDAC relative to that of carbohydrate antigen 19-9 (CA19-9). Methods: ctDNA analysis using a targeted next-generation sequencing panel was performed at baseline and during chemotherapy response evaluation in 53 patients. Progression-free survival (PFS) and overall survival (OS) were first evaluated based on ctDNA positivity at baseline. For further comparison, patients testing ctDNA-positive at baseline were subdivided based on residual ctDNA into ctDNA responders (no residual ctDNA post-chemotherapy) and ctDNA non-responders (residual ctDNA post-chemotherapy). Additional survival analysis was performed based on CA19-9 levels. Results: The baseline ctDNA detection rate was 56.6%. Although clinical outcomes tended to be poorer in patients with baseline ctDNA positivity than in those without, the differences were not significant. Residual ctDNA post-chemotherapy was associated with reduced PFS and OS. The prognosis of ctDNA responders was better than that of non-responders but did not significantly differ from that of ctDNA-negative individuals (no ctDNA both at baseline and during post-chemotherapy). Compared with ctDNA responses to chemotherapy, a >= 50% decrease in the CA19-9 level had less effect on both PFS and OS based on hazard ratios and significance levels. ctDNA could be monitored in half of the patients whose baseline CA19-9 levels were within the reference range. Conclusions: Residual ctDNA analysis post-chemotherapy is a promising approach for predicting the clinical outcomes of patients with metastatic PDAC.-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherKorean Society for Laboratory Medicine-
dc.relation.isPartOfANNALS OF LABORATORY MEDICINE-
dc.relation.isPartOfANNALS OF LABORATORY MEDICINE-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBiomarkers, Tumor / blood-
dc.subject.MESHBiomarkers, Tumor / genetics-
dc.subject.MESHCA-19-9 Antigen / blood-
dc.subject.MESHCarcinoma, Pancreatic Ductal* / diagnosis-
dc.subject.MESHCarcinoma, Pancreatic Ductal* / drug therapy-
dc.subject.MESHCarcinoma, Pancreatic Ductal* / mortality-
dc.subject.MESHCarcinoma, Pancreatic Ductal* / pathology-
dc.subject.MESHCirculating Tumor DNA* / blood-
dc.subject.MESHFemale-
dc.subject.MESHHigh-Throughput Nucleotide Sequencing-
dc.subject.MESHHumans-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Metastasis-
dc.subject.MESHPancreatic Neoplasms* / diagnosis-
dc.subject.MESHPancreatic Neoplasms* / drug therapy-
dc.subject.MESHPancreatic Neoplasms* / mortality-
dc.subject.MESHPancreatic Neoplasms* / pathology-
dc.subject.MESHPrognosis-
dc.titlePrognostic Value of Residual Circulating Tumor DNA in Metastatic Pancreatic Ductal Adenocarcinoma-
dc.typeArticle-
dc.contributor.googleauthorKim, Hongkyung-
dc.contributor.googleauthorLee, Jinho-
dc.contributor.googleauthorPark, Mi Ri-
dc.contributor.googleauthorChoi, Zisun-
dc.contributor.googleauthorHan, Seung Jung-
dc.contributor.googleauthorKim, Dongha-
dc.contributor.googleauthorShin, Saeam-
dc.contributor.googleauthorLee, Seung-Tae-
dc.contributor.googleauthorChoi, Jong Rak-
dc.contributor.googleauthorPark, Seung Woo-
dc.identifier.doi10.3343/alm.2024.0345-
dc.relation.journalcodeJ00164-
dc.identifier.eissn2234-3814-
dc.identifier.pmid39801270-
dc.subject.keywordBiomarkers-
dc.subject.keywordCA19-9-
dc.subject.keywordCirculating tumor DNA-
dc.subject.keywordNeoplasm metastasis-
dc.subject.keywordPancreatic ductal adenocarcinoma-
dc.subject.keywordPrognosis-
dc.subject.keywordResidual neoplasm-
dc.contributor.affiliatedAuthorLee, Jinho-
dc.contributor.affiliatedAuthorPark, Mi Ri-
dc.contributor.affiliatedAuthorShin, Saeam-
dc.contributor.affiliatedAuthorLee, Seung-Tae-
dc.contributor.affiliatedAuthorChoi, Jong Rak-
dc.contributor.affiliatedAuthorPark, Seung Woo-
dc.identifier.scopusid2-s2.0-85216715666-
dc.identifier.wosid001428086200009-
dc.citation.volume45-
dc.citation.number2-
dc.citation.startPage199-
dc.citation.endPage208-
dc.identifier.bibliographicCitationANNALS OF LABORATORY MEDICINE, Vol.45(2) : 199-208, 2025-03-
dc.identifier.rimsid88202-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorBiomarkers-
dc.subject.keywordAuthorCA19-9-
dc.subject.keywordAuthorCirculating tumor DNA-
dc.subject.keywordAuthorNeoplasm metastasis-
dc.subject.keywordAuthorPancreatic ductal adenocarcinoma-
dc.subject.keywordAuthorPrognosis-
dc.subject.keywordAuthorResidual neoplasm-
dc.subject.keywordPlusCARBOHYDRATE ANTIGEN 19-9-
dc.subject.keywordPlusCANCER INCIDENCE-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusCA-19-9-
dc.subject.keywordPlusDEATHS-
dc.subject.keywordPlusCTDNA-
dc.type.docTypeArticle-
dc.identifier.kciidART003174007-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalWebOfScienceCategoryMedical Laboratory Technology-
dc.relation.journalResearchAreaMedical Laboratory Technology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.