Immunophenotype based on inflammatory cells, PD-1/PD-L1 signalling pathway and M2 macrophages predicts survival in gastric cancer

dc.contributor.authorJunttila Anna
dc.contributor.authorHelminen Olli
dc.contributor.authorVäyrynen Juha P.
dc.contributor.authorAhtiainen Maarit
dc.contributor.authorKenessey Istvan
dc.contributor.authorJalkanen Sirpa
dc.contributor.authorMecklin Jukka-Pekka
dc.contributor.authorKellokumpu Ilmo
dc.contributor.authorKuopio Teijo
dc.contributor.authorBöhm Jan
dc.contributor.authorMrena Johanna
dc.contributor.organizationfi=MediCity|en=MediCity|
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.contributor.organization-code1.2.246.10.2458963.20.83772236069
dc.contributor.organization-code2607003
dc.converis.publication-id50476259
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/50476259
dc.date.accessioned2022-10-28T13:20:33Z
dc.date.available2022-10-28T13:20:33Z
dc.description.abstract<p>Background</p><p>Immune response against cancer has prognostic impact but its role in gastric cancer is poorly known. The aim of the study was to assess the prognostic significance of immune cell score (CD3+, CD8+), tumour immune escape (PD-L1, PD-1) and immune tolerance (Clever-1). </p><p>Methods<br>After exclusion of Epstein-Barr virus positive (n = 4) and microsatellite instable (n = 6) tumours, the study included 122 patients with GC undergoing D2 gastrectomy. CD3+ and CD8+ based ICS, PD-L1, PD-1 and Clever-1 expressions were evaluated. Differences in survival were examined using Cox regression adjusted for confounders. The primary outcome was 5-year survival. <br></p><p>Results <br></p><p>The 5-year overall survival rate was 43.4%. High ICS was associated with improved overall survival (adjusted HR 0.48 (95% CI 0.26-0.87)) compared to low ICS. In the high ICS group, patients with PD-L1 expression (5-year survival 69.2 vs. 53.1%, <em>p</em> = 0.317), high PD-1 (5-year survival 70.6 vs. 55.3% <em>p</em> = 0.312) and high Clever-1 (5-year survival 72.0% vs. 45.5% (<em>p</em> = 0.070) had poor prognosis. <br></p><p>Conclusions <br></p><p>High ICS was associated with improved survival. In the high ICS group, patients with high PD-L1, PD-1 and Clever-1 had poor prognosis highlighting the importance of immune escape and immune tolerance in GC.</p>
dc.format.pagerange1625
dc.format.pagerange1632
dc.identifier.eissn1532-1827
dc.identifier.jour-issn0007-0920
dc.identifier.olddbid181400
dc.identifier.oldhandle10024/164494
dc.identifier.urihttps://www.utupub.fi/handle/11111/37929
dc.identifier.urnURN:NBN:fi-fe2021042826535
dc.language.isoen
dc.okm.affiliatedauthorKenessey, Istvan
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.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNATURE PUBLISHING GROUP
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1038/s41416-020-01053-7
dc.relation.ispartofjournalBritish Journal of Cancer
dc.relation.issue11
dc.relation.volume123
dc.source.identifierhttps://www.utupub.fi/handle/10024/164494
dc.titleImmunophenotype based on inflammatory cells, PD-1/PD-L1 signalling pathway and M2 macrophages predicts survival in gastric cancer
dc.year.issued2020

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