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Cited 21 time in webofscience Cited 22 time in scopus
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Vitamin D status after colorectal cancer diagnosis and patient survival according to immune response to tumour

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dc.contributor.authorHamada, Tsuyoshi-
dc.contributor.authorLiu, Li-
dc.contributor.authorNowak, Jonathan A.-
dc.contributor.authorMima, Kosuke-
dc.contributor.authorCao, Yin-
dc.contributor.authorNg, Kimmie-
dc.contributor.authorTwombly, Tyler S.-
dc.contributor.authorSong, Mingyang-
dc.contributor.authorJung, Seungyoun-
dc.contributor.authorDou, Ruoxu-
dc.contributor.authorMasugi, Yohei-
dc.contributor.authorKosumi, Keisuke-
dc.contributor.authorShi, Yan-
dc.contributor.authorda Silva, Annacarolina-
dc.contributor.authorGu, Mancang-
dc.contributor.authorLi, Wanwan-
dc.contributor.authorKeum, NaNa-
dc.contributor.authorWu, Kana-
dc.contributor.authorNosho, Katsuhiko-
dc.contributor.authorInamura, Kentaro-
dc.contributor.authorMeyerhardt, Jeffrey A.-
dc.contributor.authorNevo, Daniel-
dc.contributor.authorWang, Molin-
dc.contributor.authorGiannakis, Marios-
dc.contributor.authorChan, Andrew T.-
dc.contributor.authorGiovannucci, Edward L.-
dc.contributor.authorFuchs, Charles S.-
dc.contributor.authorNishihara, Reiko-
dc.contributor.authorZhang, Xuehong-
dc.contributor.authorOgino, Shuji-
dc.date.accessioned2023-04-28T06:42:03Z-
dc.date.available2023-04-28T06:42:03Z-
dc.date.issued2018-11-
dc.identifier.issn0959-8049-
dc.identifier.issn1879-0852-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/8935-
dc.description.abstractBackground: High-level plasma 25-hydroxyvitamin D[25(OH)D] has been associated with lower colorectal cancer incidence and mortality. Considering evidence indicating immunomodulatory effects of vitamin D, we hypothesised that survival benefits from high systemic vitamin D level might be stronger for colorectal carcinoma with lower immune response to tumour. Methods: Using 869 colon and rectal cancer cases within the Nurses' Health Study and Health Professionals Follow-up Study, we assessed the prognostic association of postdiagnosis 25(OH) D score [derived from diet and lifestyle variables to predict plasma 25(OH) D level] in strata of levels of histopathologic lymphocytic reaction. The Cox proportional hazards regression model was adjusted for potential confounders, including microsatellite instability, CpG island methylator phenotype, LINE-1 methylation, PTGS2 (cyclooxygenase-2) expression and KRAS, BRAF and PIK3CA mutations. Results: The association of postdiagnosis 25(OH) D score with colorectal cancer-specific mortality differed by levels of peritumoural lymphocytic reaction (p(interaction) = 0.001). Multivariable-adjusted mortality hazard ratios for a quintile-unit increase of 25(OH) D score were 0.69 [95% confidence interval (CI), 0.54-0.89] in cases with negative/low peritumoural lymphocytic reaction, 1.08 (95% CI, 0.93-1.26) in cases with intermediate peritumoural reaction and 1.25 (95% CI, 0.75-2.09) in cases with high peritumoural reaction. The survival association of the 25(OH) D score did not significantly differ by Crohn's-like lymphoid reaction, intratumoural periglandular reaction or tumour-infiltrating lymphocytes. Conclusions: The association between the 25(OH) D score and colorectal cancer survival is stronger for carcinomas with lower peritumoural lymphocytic reaction. Our results suggesting interactive effects of vitamin D and immune response may contribute to personalised dietary and lifestyle intervention strategies. (C) 2018 Elsevier Ltd. All rights reserved.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCI LTD-
dc.titleVitamin D status after colorectal cancer diagnosis and patient survival according to immune response to tumour-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.ejca.2018.07.130-
dc.identifier.scopusid2-s2.0-85053203682-
dc.identifier.wosid000447292100012-
dc.identifier.bibliographicCitationEUROPEAN JOURNAL OF CANCER, v.103, pp 98 - 107-
dc.citation.titleEUROPEAN JOURNAL OF CANCER-
dc.citation.volume103-
dc.citation.startPage98-
dc.citation.endPage107-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusIMMUNOTHERAPY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROGNOSIS-
dc.subject.keywordPlusMORTALITY-
dc.subject.keywordPlusASPIRIN-
dc.subject.keywordPlusRISK-
dc.subject.keywordAuthorClinical outcome-
dc.subject.keywordAuthorImmunology-
dc.subject.keywordAuthorMolecular pathological epidemiology-
dc.subject.keywordAuthorPrecision medicine-
dc.subject.keywordAuthorTumour microenvironment-
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