Tumor-associated CD3- and CD8-positive immune cells in colorectal cancer: The additional prognostic value of CD8+-to-CD3+ ratio remains debatable

dc.contributor.authorKasurinen Jussi
dc.contributor.authorHagström Jaana
dc.contributor.authorKaprio Tuomas
dc.contributor.authorBeilmann-Lehtonen Ines
dc.contributor.authorHaglund Caj
dc.contributor.authorBöckelman Camilla
dc.contributor.organizationfi=hammaslääketieteen laitos|en=Institute of Dentistry|
dc.contributor.organization-code1.2.246.10.2458963.20.64787032594
dc.converis.publication-id175288291
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175288291
dc.date.accessioned2022-10-28T12:46:07Z
dc.date.available2022-10-28T12:46:07Z
dc.description.abstract<p>Background<br></p><p>A large number of infiltrating CD3- and CD8-positive inflammatory cells indicates an improved survival in colorectal cancer (CRC), similar to many other cancers.<br></p><p>Objective<br></p><p>We investigated the prognostic value of different combinations of CD3- and CD8-positive immune cells in CRC patients.<br></p><p>Methods<br></p><p>The densities of CD3- and CD8-positive cells in intratumoral and stromal tissues were evaluated from 539 patients, for which we calculated a CD3 tumor–stroma index, a CD8 tumor–stroma index, and a CD3–CD8 tumor–stroma index.<br></p><p>Results<br></p><p>High CD3 and CD8 tumor–stroma indices associated with stage I to II disease (<i>p</i> < 0.001 for both). The CD3 tumor–stroma index associated with a colonic tumor location (<i>p</i> = 0.006), while the CD8 tumor–stroma index associated with right-sided tumors (<i>p</i> < 0.001) and histological grade 3 tumors (<i>p</i> = 0.032). High intratumoral and stromal densities for CD3- and CD8-positive immune cells, the CD3 tumor–stroma index, the CD8 tumor–stroma index, and the CD3–CD8 tumor–stroma index all indicated a better DSS.<br></p><p>Conclusions<br></p><p>The CD3 tumor–stroma index carries a strong prognostic value in CRC, and none of the CD3 and CD8 combinations we analyzed proved superior.<br></p>
dc.format.pagerange37
dc.format.pagerange52
dc.identifier.eissn1423-0380
dc.identifier.jour-issn1010-4283
dc.identifier.olddbid178823
dc.identifier.oldhandle10024/161917
dc.identifier.urihttps://www.utupub.fi/handle/11111/36413
dc.identifier.urlhttps://content.iospress.com/articles/tumor-biology/tub211571
dc.identifier.urnURN:NBN:fi-fe2022081154200
dc.language.isoen
dc.okm.affiliatedauthorHagström, Jaana
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherIOS Press BV
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.doi10.3233/TUB-211571
dc.relation.ispartofjournalTumor Biology
dc.relation.issue1
dc.relation.volume44
dc.source.identifierhttps://www.utupub.fi/handle/10024/161917
dc.titleTumor-associated CD3- and CD8-positive immune cells in colorectal cancer: The additional prognostic value of CD8+-to-CD3+ ratio remains debatable
dc.year.issued2022

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