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Claudin 18.2, IDH1, and neutrophil-to-lymphocyte ratio as prognostic biomarkers in unresectable pancreatic ductal adenocarcinoma receiving first-line chemotherapy

dc.contributor.authorKarcl, Ebru
dc.contributor.authorOzden, Ferhat
dc.contributor.authorKuzucular, Elif
dc.contributor.authorAcikgoz, Ozgur
dc.contributor.authorOlmez, Omer Fatih
dc.contributor.authorYildiz, Ozcan
dc.contributor.authorUzun, Hafize
dc.contributor.authorBilici, Ahmet
dc.date.accessioned2026-11-05T11:07:01Z
dc.date.issued2026
dc.description.abstractPancreatic ductal adenocarcinoma (PDAC) is a highly aggressive malignancy with few effective treatment options. This study investigates the prognostic significance of claudin 18.2 (CLDN18.2), isocitrate dehydrogenase-1 (IDH1) expression, and the neutrophil-to-lymphocyte ratio (NLR) in patients with unresectable PDAC undergoing first-line chemotherapy. This single-center retrospective analysis utilized prospectively collected data from 72 patients treated with FOLFIRINOX (59.7%) or gemcitabine plus nab-paclitaxel (40.3%). CLDN18.2 and IDH1 expression levels were evaluated through immunohistochemistry, while NLR was calculated from pretreatment blood counts. Survival analyses were conducted using univariable and multivariable Cox regression models. CLDN18.2 positivity was found in 18.1% of patients, and IDH1 positivity was observed in 2.8%. Additionally, an elevated NLR (>3.22) was present in 56.9% of patients. The median progression-free survival (PFS) and overall survival (OS) were 7.1 months (95% CI: 4.2-9.9) and 9.7 months (95% CI: 8.5-10.8), respectively. In the multivariable analysis, CLDN18.2 expression, IDH1 expression, and NLR were significantly associated with OS, whereas no consistent associations were found for PFS. Effect estimates include corresponding 95% confidence intervals. These findings indicate the potential prognostic value of integrating molecular and systemic biomarkers in unresectable PDAC. However, due to the retrospective design and limited sample size, these results should be regarded as hypothesis-generating and necessitate validation in larger, independent cohorts prior to clinical implementation.
dc.description.issue11
dc.description.pages2117-2124
dc.description.volume26
dc.identifier.doi10.17305/bb.2026.14093
dc.identifier.issn2831-0896
dc.identifier.issn2831-090X
dc.identifier.urihttps://doi.org/10.17305/bb.2026.14093
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/11410
dc.identifier.wosWOS:001740306300001
dc.language.isoen
dc.publisherASSOC BASIC MEDICAL SCI FEDERATION BOSNIA & HERZEGOVINA SARAJEVO
dc.relation.hasversion10.17305/bb.2026.14093
dc.relation.ispartofBIOMOLECULES AND BIOMEDICINE
dc.subjectPancreatic ductal adenocarcinoma
dc.subjectclaudin 18.2
dc.subjectisocitrate dehydrogenase
dc.subjectneutrophil-to-lymphocyte ratio
dc.subjectprognosis
dc.subjectoverall survival
dc.subjectCANCER
dc.subjectANTIBODY
dc.subjectTARGET
dc.subjectMedicine, Research & Experimental
dc.subjectResearch & Experimental Medicine
dc.titleClaudin 18.2, IDH1, and neutrophil-to-lymphocyte ratio as prognostic biomarkers in unresectable pancreatic ductal adenocarcinoma receiving first-line chemotherapy
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.endPage2124
oaire.citation.issue11
oaire.citation.startPage2117
oaire.citation.volume26
person.identifier.ridHZK-7453-2023

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