Pancreatic cancer survival prediction via inflammatory serum markers

dc.contributor.authorLanki Mira
dc.contributor.authorSeppänen Hanna
dc.contributor.authorMustonen Harri
dc.contributor.authorSalmiheimo Aino
dc.contributor.authorStenman Ulf-Håkan
dc.contributor.authorSalmi Marko
dc.contributor.authorJalkanen Sirpa
dc.contributor.authorHaglund Caj
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.contributor.organization-code1.2.246.10.2458963.20.83772236069
dc.converis.publication-id69283728
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/69283728
dc.date.accessioned2022-10-28T12:48:14Z
dc.date.available2022-10-28T12:48:14Z
dc.description.abstract<p><strong>Background: </strong>For prognostic evaluation of pancreatic ductal adenocarcinoma (PDAC), the only well-established serum marker is carbohydrate antigen CA19-9. To improve the accuracy of survival prediction, we tested the efficacy of inflammatory serum markers.</p><p><strong>Methods: </strong>A preoperative serum panel comprising 48 cytokines plus high-sensitivity CRP (hs-CRP) was analyzed in 173 stage I-III PDAC patients. Analysis of the effect of serum markers on survival utilized the Cox regression model, with the most promising cytokines chosen with the aid of the lasso method. We formed a reference model comprising age, gender, tumor stage, adjuvant chemotherapy status, and CA19-9 level. Our prognostic study model incorporated these data plus hs-CRP and the cytokines. We constructed time-dependent ROC curves and calculated an integrated time-averaged area under the curve (iAUC) for both models from 1 to 10 years after surgery.</p><p><strong>Results: </strong>Hs-CRP and the cytokines CTACK, MIF, IL-1β, IL-3, GRO-α, M-CSF, and SCF, were our choices for the prognostic study model, in which the iAUC was 0.837 (95% CI 0.796-0.902), compared to the reference model's 0.759 (95% CI 0.691-0.836, NS). These models divided the patients into two groups based on the maximum value of Youden's index at 7.5 years. In our study model, 60th percentile survival times were 4.5 (95% CI 3.7-NA) years (predicted high-survival group, n = 34) and 1.3 (95% CI 1.0-1.7) years (predicted low-survival group, n = 128), log rank p < 0.001. By the reference model, the 60th percentile survival times were 2.8 (95% CI 2.1-4.4) years (predicted high-survival group, n = 44) and 1.3 (95% CI 1.0-1.7) years (predicted low-survival group, n = 118), log rank p < 0.001.</p><p><strong>Conclusion: </strong>Hs-CRP and the seven cytokines added to the reference model including CA19-9 are potential prognostic factors for improved survival prediction for PDAC patients.</p>
dc.identifier.jour-issn0340-7004
dc.identifier.olddbid179094
dc.identifier.oldhandle10024/162188
dc.identifier.urihttps://www.utupub.fi/handle/11111/33512
dc.identifier.urnURN:NBN:fi-fe2022022120288
dc.language.isoen
dc.okm.affiliatedauthorSalmi, Marko
dc.okm.affiliatedauthorJalkanen, Sirpa
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSPRINGER
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1007/s00262-021-03137-6
dc.relation.ispartofjournalCancer Immunology, Immunotherapy
dc.source.identifierhttps://www.utupub.fi/handle/10024/162188
dc.titlePancreatic cancer survival prediction via inflammatory serum markers
dc.year.issued2022

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