dc.contributor.author | Ree, Anne Hansen | |
dc.contributor.author | Nygaard, Vigdis | |
dc.contributor.author | Russnes, Hege Elisabeth Giercksky | |
dc.contributor.author | Heinrich, Daniel | |
dc.contributor.author | Nygaard, Vegard | |
dc.contributor.author | Johansen, Christin | |
dc.contributor.author | Bergheim, Inger Riise | |
dc.contributor.author | Hovig, Eivind | |
dc.contributor.author | Beiske, Klaus | |
dc.contributor.author | Negård, Anne | |
dc.contributor.author | Børresen-Dale, Anne-Lise | |
dc.contributor.author | Flatmark, Kjersti | |
dc.contributor.author | Mælandsmo, Gunhild Mari | |
dc.date.accessioned | 2020-02-03T14:07:49Z | |
dc.date.available | 2020-02-03T14:07:49Z | |
dc.date.issued | 2019-02-25 | |
dc.description.abstract | Most 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.citation | Ree 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):701-706 | en_US |
dc.identifier.cristinID | FRIDAID 1707183 | |
dc.identifier.doi | 10.1158/2326-6066.CIR-18-0777 | |
dc.identifier.issn | 2326-6066 | |
dc.identifier.issn | 2326-6074 | |
dc.identifier.uri | https://hdl.handle.net/10037/17310 | |
dc.language.iso | eng | en_US |
dc.publisher | American Association for Cancer Research | en_US |
dc.relation.journal | Cancer immunology research | |
dc.relation.projectID | Norges forskningsråd: 218325 | en_US |
dc.relation.projectID | Helse Sør-Øst RHF: 2017109 | en_US |
dc.relation.projectID | info: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.accessRights | openAccess | en_US |
dc.rights.holder | ©2019 American Association for Cancer Research. | en_US |
dc.subject | VDP::Medisinske Fag: 700 | |
dc.subject | VDP::Medical disciplines: 700 | |
dc.title | Responsiveness to PD-1 Blockade in End-Stage Colon Cancer with Gene Locus 9p24.1 Copy-Number Gain | en_US |
dc.type.version | acceptedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |