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dc.contributor.authorBirkman, Eva-Maria
dc.contributor.authorAvoranta, Tuulia
dc.contributor.authorÅlgars, Annika
dc.contributor.authorKorkeila, Eija
dc.contributor.authorLintunen, Minnamaija
dc.contributor.authorLahtinen, Laura
dc.contributor.authorKuopio, Teijo
dc.contributor.authorRistamäki, Raija
dc.contributor.authorCarpén, Olli
dc.contributor.authorSundström, Jari
dc.date.accessioned2018-10-30T10:44:32Z
dc.date.available2018-10-30T10:44:32Z
dc.date.issued2018
dc.identifier.citationBirkman, E.-M., Avoranta, T., Ålgars, A., Korkeila, E., Lintunen, M., Lahtinen, L., Kuopio, T., Ristamäki, R., Carpén, O., & Sundström, J. (2018). EGFR gene copy number decreases during anti-EGFR antibody therapy in colorectal cancer. <i>Human Pathology</i>, <i>82</i>, 163-171. <a href="https://doi.org/10.1016/j.humpath.2018.07.028" target="_blank">https://doi.org/10.1016/j.humpath.2018.07.028</a>
dc.identifier.otherCONVID_28219805
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/60025
dc.description.abstractEpidermal growth factor receptor (EGFR) gene copy number (GCN) increase is associated with a favorable anti-EGFR antibody treatment response in RAS wild-type metastatic colorectal cancer. However, there are limited and comparative data regarding the EGFR GCN in primary colorectal cancer tumors and corresponding metastases or the effect of anti-EGFR antibody treatment on EGFR GCN in recurrent disease. In addition, little is known about the potential EGFR GCN changes during anti-EGFR therapy in comparison with other treatment regimens. EGFR GCN was analyzed by EGFR immunohistochemistry-guided silver in situ hybridization in primary and corresponding recurrent local or metastatic tumors from 80 colorectal cancer patients. GCN levels were compared between KRAS wild-type patients having received anti-EGFR therapy and patients having received other forms of treatment after primary surgery. The EGFR GCN decrease between primary and recurrent tumors was more pronounced among the anti–EGFR-treated patients than among patients not treated with anti-EGFR therapy (P = .047). None of the patients experiencing an EGFR GCN increase of at least 1.0 between the primary and recurrent tumors were treated with anti-EGFR antibodies. When including only patients with distant metastases, an EGFR GCN decrease of at least 1.0 was more common among the anti–EGFR-treated patients than among patients not treated with anti-EGFR therapy (P = .028). Our results suggest that anti-EGFR antibody treatment is associated with EGFR GCN decrease between the primary and recurrent colorectal adenocarcinomas, whereas no GCN change is observed among patients receiving other forms of treatment after primary surgery.fi
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherElsevier Inc.
dc.relation.ispartofseriesHuman Pathology
dc.rightsCC BY-NC-ND 4.0
dc.subject.othercolorectal cancer
dc.subject.otherepidermal growth factor receptor
dc.subject.othergene copy number
dc.subject.othersilver in situ hybridization
dc.subject.othermonoclonal antibody
dc.titleEGFR gene copy number decreases during anti-EGFR antibody therapy in colorectal cancer
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-201810304553
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.contributor.oppiaineSolu- ja molekyylibiologiafi
dc.contributor.oppiaineCell and Molecular Biologyen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2018-10-30T10:15:13Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange163-171
dc.relation.issn0046-8177
dc.relation.numberinseries0
dc.relation.volume82
dc.type.versionpublishedVersion
dc.rights.copyright© 2018 the Authors
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.subject.ysoperäsuolisyöpä
dc.subject.ysosyöpähoidot
dc.subject.ysovasta-aineet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p5936
jyx.subject.urihttp://www.yso.fi/onto/yso/p27422
jyx.subject.urihttp://www.yso.fi/onto/yso/p12206
dc.rights.urlhttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.relation.doi10.1016/j.humpath.2018.07.028
dc.type.okmA1


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