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dc.contributor.authorRee, Anne Hansen
dc.contributor.authorNygaard, Vigdis
dc.contributor.authorRussnes, Hege Elisabeth Giercksky
dc.contributor.authorHeinrich, Daniel
dc.contributor.authorNygaard, Vegard
dc.contributor.authorJohansen, Christin
dc.contributor.authorBergheim, Inger Riise
dc.contributor.authorHovig, Eivind
dc.contributor.authorBeiske, Klaus
dc.contributor.authorNegård, Anne
dc.contributor.authorBørresen-Dale, Anne-Lise
dc.contributor.authorFlatmark, Kjersti
dc.contributor.authorMælandsmo, Gunhild Mari
dc.date.accessioned2020-02-03T14:07:49Z
dc.date.available2020-02-03T14:07:49Z
dc.date.issued2019-02-25
dc.description.abstractMost patients whose large bowel cancer has spread to other organs do not respond to immune therapy. We detected a rare gene mutation, termed 9p24.1 copy-number gain (CNG), in an otherwise incurable colorectal cancer that provoked an immune therapy response. We identified this gene mutation by gene-panel sequencing of DNA from a liver metastasis biopsy from a patient who had disease refractory to standard therapies. Following immune checkpoint blockade (ICB) with pembrolizumab (anti–PD-1), the patient experienced conversion of the tumor phenotype from one with epithelial features to that of an inflamed microenvironment, detected by high-resolution RNA sequencing. Circulating tumor DNA disappeared over the first weeks of therapy. As assessed by standard radiographic measurement, the patient had a partial response that was durable. This patient's response may support the use of histology-agnostic ICB in solid tumors that carry the rare 9p24.1 CNG.en_US
dc.identifier.citationRee AH, Nygaard V, Russnes HE, Heinrich D, Nygaard V, Johansen C, Bergheim IR, Hovig E, Beiske K, Negård A, Børresen-Dale A, Flatmark K, Mælandsmo GM. Responsiveness to PD-1 Blockade in End-Stage Colon Cancer with Gene Locus 9p24.1 Copy-Number Gain. Cancer immunology research. 2019;7(5):701-706en_US
dc.identifier.cristinIDFRIDAID 1707183
dc.identifier.doi10.1158/2326-6066.CIR-18-0777
dc.identifier.issn2326-6066
dc.identifier.issn2326-6074
dc.identifier.urihttps://hdl.handle.net/10037/17310
dc.language.isoengen_US
dc.publisherAmerican Association for Cancer Researchen_US
dc.relation.journalCancer immunology research
dc.relation.projectIDNorges forskningsråd: 218325en_US
dc.relation.projectIDHelse Sør-Øst RHF: 2017109en_US
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN/BEHANDLING/218325/Norway/MetAction: Actionable Targets in Cancer Metastasis - from Bed to Bench to Byte to Bedside//en_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holder©2019 American Association for Cancer Research.en_US
dc.subjectVDP::Medisinske Fag: 700
dc.subjectVDP::Medical disciplines: 700
dc.titleResponsiveness to PD-1 Blockade in End-Stage Colon Cancer with Gene Locus 9p24.1 Copy-Number Gainen_US
dc.type.versionacceptedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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