Serum cytokine profiles in patients with pancreatic cancer and chronic pancreatitis

dc.contributor.authorLanki Mira
dc.contributor.authorMustonen Harri
dc.contributor.authorSalmi Marko
dc.contributor.authorJalkanen Sirpa
dc.contributor.authorHaglund Caj
dc.contributor.authorSeppänen Hanna
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=MediCity|en=MediCity|
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id180486722
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/180486722
dc.date.accessioned2025-08-27T12:56:25Z
dc.date.available2025-08-27T12:56:25Z
dc.description.abstract<p>Background: Chronic pancreatitis (CP) may cause tumor-like lesions, creating a challenge in distinguishing between CP and pancreatic ductal adenocarcinoma (PDAC) in a patient. Given that invasive surgery is a standard cancer treatment, we aimed to examine whether a noninvasive diagnostic tool utilizing serum cytokines could safely differentiate between PDAC and CP.</p><p><i>Methods:</i> A pre-operative serum panel comprising 48 inflammatory cytokines, CA19-9, and C-reactive protein (CRP) was analyzed, consisting of 231 patients, 186 with stage IeIII PDAC and 45 with CP. We excluded PDAC patients who underwent neoadjuvant therapy and those CP patients with other active malignancies. The laboratory variables most associated with PDAC diagnosis were assessed using logistic regression and selected using the lasso method.<br></p><p><i>Results</i>: The cytokines CTACK, GRO-a, and b-NGF were selected alongside CA19-9 and CRP for our differential diagnostic model. The area under the curve (AUC) for our differential diagnostic model was 0.809 (95% confidence interval [CI] 0.738e0.880), compared with 0.791 (95% CI 0.728e0.854) for CA19-9 alone (not significant).<br></p><p><i>Conclusions</i>: We found that inflammatory cytokines CTACK, GRO-a, and b-NGF alongside CA19-9 and CRP may help distinguish PDAC from CP.<br></p>
dc.identifier.eissn1424-3911
dc.identifier.jour-issn1424-3903
dc.identifier.olddbid199899
dc.identifier.oldhandle10024/182926
dc.identifier.urihttps://www.utupub.fi/handle/11111/45093
dc.identifier.urlhttps://doi.org/10.1016/j.pan.2023.07.004
dc.identifier.urnURN:NBN:fi-fe2025082784834
dc.language.isoen
dc.okm.affiliatedauthorSalmi, Marko
dc.okm.affiliatedauthorJalkanen, Sirpa
dc.okm.affiliatedauthorDataimport, MediCity
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier B.V.
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.doi10.1016/j.pan.2023.07.004
dc.relation.ispartofjournalPancreatology
dc.source.identifierhttps://www.utupub.fi/handle/10024/182926
dc.titleSerum cytokine profiles in patients with pancreatic cancer and chronic pancreatitis
dc.year.issued2023

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