CA125: A superior prognostic biomarker for colorectal cancer compared to CEA, CA19-9 or CA242

dc.contributor.authorBjörkman Kajsa
dc.contributor.authorMustonen Harri
dc.contributor.authorKaprio Tuomas
dc.contributor.authorKekki Henna
dc.contributor.authorPettersson Kim
dc.contributor.authorHaglund Caj
dc.contributor.authorBöckelman Camilla
dc.contributor.organizationfi=MediCity|en=MediCity|
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=biotekniikka|en=Biotechnology|
dc.contributor.organization-code1.2.246.10.2458963.20.98373201676
dc.converis.publication-id62086113
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/62086113
dc.date.accessioned2022-10-28T13:51:41Z
dc.date.available2022-10-28T13:51:41Z
dc.description.abstract<p>OBJECTIVES:<br>The tumor stage represents the single most important prognostic factor for colorectal cancer (CRC), although more accurate prognostics remain much needed. Previously, we identified CA125 as an independent significant prognostic factor, which we have further validated along with CEA, CA19-9, and CA242 in a large cohort of CRC patients.<br>METHODS:<br>Using enzyme-linked immunosorbent assays, we analyzed preoperative serum samples in 322 CRC patients operated on between 1998 and 2003.<br>RESULTS:<br>Using the Spearman’s rho model, we calculated the correlation between our previous findings on MUC16 and CA125, for which the correlation coefficient was 0.808 (p < 0.001). The Cox regression analysis of the linear and logarithmic values of CEA, CA125, CA242, and CA19-9 identified only CA125 (hazard ratio [HR] 1.03; 95% confidence interval [95% CI] 1.02−1.04; p < 0.001) as significant when using the linear values. Survival among CRC patients with a high CA125 level was poor compared with CRC patients with a low CA125 level (HR 2.48; 95% CI 1.68–3.65; p < 0.001). In subgroup analyses, patients with high CA125 levels and aged ≤67 or >67, with stage I–II or III–IV, and both colon and rectal cancer exhibited poor prognoses. In the multivariate analysis, we used clinical pathological variables in the model, where age, gender, and stage served as the background characteristics. We dichotomized CA125 using the Youden maximal cutoff point, and the median values for CEA, CA19-9, and CA242. CA125 emerged as the only marker remaining significant and independent together with stage, location, and age (HR 1.91; 95% CI 1.24–2.95; p 0.003).<br>CONCLUSIONS:<br>CA125 represents a significant and independent prognostic factor in CRC patients, superior to CEA. Furthermore, CA242 served as a better prognostic marker than both CEA and CA19-9. We recommend including both CA125 and CA242 in prognostic clinical trials among CRC patients.<br></p>
dc.format.pagerange57
dc.format.pagerange70
dc.identifier.eissn1423-0380
dc.identifier.jour-issn1010-4283
dc.identifier.olddbid184801
dc.identifier.oldhandle10024/167895
dc.identifier.urihttps://www.utupub.fi/handle/11111/40944
dc.identifier.urlhttps://content.iospress.com/articles/tumor-biology/tub200069
dc.identifier.urnURN:NBN:fi-fe2021093048808
dc.language.isoen
dc.okm.affiliatedauthorDataimport, MediCity
dc.okm.affiliatedauthorDataimport, Biolääketieteen laitoksen yhteiset
dc.okm.affiliatedauthorKekki, Henna
dc.okm.affiliatedauthorPettersson, Kim
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.publisherNLM (Medline)
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.doi10.3233/TUB-200069
dc.relation.ispartofjournalTumor Biology
dc.relation.issue1
dc.relation.volume43
dc.source.identifierhttps://www.utupub.fi/handle/10024/167895
dc.titleCA125: A superior prognostic biomarker for colorectal cancer compared to CEA, CA19-9 or CA242
dc.year.issued2021

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