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

Authors
 Kim, Hongkyung  ;  Lee, Jinho  ;  Park, Mi Ri  ;  Choi, Zisun  ;  Han, Seung Jung  ;  Kim, Dongha  ;  Shin, Saeam  ;  Lee, Seung-Tae  ;  Choi, Jong Rak  ;  Park, Seung Woo 
Citation
 ANNALS OF LABORATORY MEDICINE, Vol.45(2) : 199-208, 2025-03 
Journal Title
ANNALS OF LABORATORY MEDICINE
ISSN
 2234-3806 
Issue Date
2025-03
MeSH
Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor / blood ; Biomarkers, Tumor / genetics ; CA-19-9 Antigen / blood ; Carcinoma, Pancreatic Ductal* / diagnosis ; Carcinoma, Pancreatic Ductal* / drug therapy ; Carcinoma, Pancreatic Ductal* / mortality ; Carcinoma, Pancreatic Ductal* / pathology ; Circulating Tumor DNA* / blood ; Female ; High-Throughput Nucleotide Sequencing ; Humans ; Kaplan-Meier Estimate ; Male ; Middle Aged ; Neoplasm Metastasis ; Pancreatic Neoplasms* / diagnosis ; Pancreatic Neoplasms* / drug therapy ; Pancreatic Neoplasms* / mortality ; Pancreatic Neoplasms* / pathology ; Prognosis
Keywords
Biomarkers ; CA19-9 ; Circulating tumor DNA ; Neoplasm metastasis ; Pancreatic ductal adenocarcinoma ; Prognosis ; Residual neoplasm
Abstract
Background: 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.
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DOI
10.3343/alm.2024.0345
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
Yonsei Authors
Park, Seung Woo(박승우) ORCID logo https://orcid.org/0000-0001-8230-964X
Shin, Saeam(신새암) ORCID logo https://orcid.org/0000-0003-1501-3923
Lee, Seung-Tae(이승태) ORCID logo https://orcid.org/0000-0003-1047-1415
Choi, Jong Rak(최종락) ORCID logo https://orcid.org/0000-0002-0608-2989
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/208825
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