Publication:
Single Dose Regorafenib-Induced Hypertensive Crisis

dc.authorscopusid26647866500
dc.authorscopusid23479972900
dc.authorscopusid56151089400
dc.authorscopusid55370691000
dc.authorscopusid36702709300
dc.authorscopusid7003323947
dc.contributor.authorYilmaz, B.
dc.contributor.authorKemal, Y.
dc.contributor.authorTeker, F.
dc.contributor.authorKut, E.
dc.contributor.authorDemirag̈, G.
dc.contributor.authorYücel, I.
dc.date.accessioned2020-06-21T09:37:40Z
dc.date.available2020-06-21T09:37:40Z
dc.date.issued2014
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Yilmaz] Bahiddin, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kemal] Yasemin, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Teker] Fatih, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kut] Engin, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Demirag̈] Güzin Gonullu, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yücel] Idris, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractGastrointestinal stromal tumors (GISTs) are uncommon tumors of the gastrointestinal (GI) tract. Regorafenib is a new multikinase inhibitor and is approved for the treatment of GISTs in patients who develop resistance to imatinib and sunitinib. The most common drug-related adverse events with regorafenib are hypertension, hand-foot skin reactions, and diarrhea. Grade IV hypertensive side effect has never been reported after a single dose. In this report, we present a case of Grade IV hypertensive side effect (hypertensive crisis and seizure) after a single dose of regorafenib. A 54-year-old male normotensive GIST patient was admitted to the emergency department with seizure and encephalopathy after the first dosage of regorafenib. His blood pressure was 240/140 mmHg upon admission. After intensive treatment with nitrate and nitroprusside, his blood pressure returned to normal levels in five days. Regorafenib was discontinued, and he did not experience hypertension again. This paper reports the first case of Grade IV hypertension after the first dosage of regorafenib. We can suggest that hypertension is an idiosyncratic side effect unrelated to the dosage. Copyright © Experimental Oncology, 2014.en_US
dc.identifier.endpage135en_US
dc.identifier.issn1812-9269
dc.identifier.issue2en_US
dc.identifier.pmid24980770
dc.identifier.scopus2-s2.0-84903790361
dc.identifier.scopusqualityQ4
dc.identifier.startpage134en_US
dc.identifier.volume36en_US
dc.language.isoenen_US
dc.publisherMorion LLC tanya_ua@morion.kiev.uaen_US
dc.relation.ispartofExperimental Oncologyen_US
dc.relation.journalExperimental Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGastrointestinal Stromal Tumoren_US
dc.subjectHypertensionen_US
dc.subjectRegorafeniben_US
dc.titleSingle Dose Regorafenib-Induced Hypertensive Crisisen_US
dc.typeArticleen_US
dspace.entity.typePublication

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