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dc.contributor.authorHannevik, Trine-Lise
dc.contributor.authorBrekke, Jorunn
dc.contributor.authorEnden, Tone Rønnaug
dc.contributor.authorFrøen, Hege
dc.contributor.authorAhmed, Herish
dc.contributor.authorJacobsen, Eva-Marie
dc.contributor.authorQuist-Paulsen, Petter
dc.contributor.authorPorojnicu, Alina Carmen
dc.contributor.authorRee, Anne Hansen
dc.contributor.authorTorfoss, Dag
dc.contributor.authorVelle, Elin Osvik
dc.contributor.authorWik, Hilde Skuterud
dc.contributor.authorGhanima, Waleed Khalid
dc.contributor.authorSandset, Per Morten
dc.contributor.authorDahm, Anders Erik A
dc.date.accessioned2022-12-14T13:10:52Z
dc.date.available2022-12-14T13:10:52Z
dc.date.created2021-01-12T21:02:10Z
dc.date.issued2020
dc.identifier.citationThrombosis Research. 2020, 196 238-244.en_US
dc.identifier.issn0049-3848
dc.identifier.urihttps://hdl.handle.net/11250/3037719
dc.description.abstractIntroduction: The direct oral anti-coagulants (DOAC) edoxaban and rivaroxaban are suggested treatment alternatives for cancer-associated venous thromboembolism (VTE) together with low molecular-weight heparins. New studies indicate that the DOAC apixaban also is an option for cancer-associated VTE. The current study assessed recurrent VTE, arterial thrombosis, bleedings and adverse events in a cohort of apixaban treated cancer patients with VTE. Materials and methods: Single-arm, interventional study of apixaban as treatment of cancer-associated VTE. Inclusion criteria were cancer with objectively verified VTE. Patients received apixaban 10 mg bid for seven days, then 5 mg bid for six months. Primary efficacy and safety outcomes were recurrent VTE and bleeding respectively. This trial is registered with ClinicalTrials.gov identifier NCT02581176. Results: We recruited 298 cancer patients with VTE. During six months treatment, recurrent VTE or death related to VTE occurred in 12 patients (4.0%, 95% confidence interval (CI) 2.1–6.9%). Major bleeding occurred in 16 patients (5.4%, 95% CI 2.8–7.9), most frequently gastrointestinal bleeding. There were no overrepresentation of major bleedings among patients with gastrointestinal cancer (7/126, 5.5%, 95% CI 2.3–11%). Twenty-six patients experienced one or more clinically relevant non-major bleedings (8.9%, 95% CI 5.5–12%). Twelve patients had arterial thrombosis (4.0%, 95% CI 2.1–6.9%), of which the majority were strokes in patients with pancreatic cancer. Death occurred in 35 patients (12%, 95% CI 8.3–16%). Conclusion: The frequency of recurrent VTE and major bleedings are in line with other studies on apixaban in cancer-associated VTE. Arterial thrombosis was a frequent serious adverse event.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.titleThrombosis and bleedings in a cohort of cancer patients treated with apixaban for venous thromboembolismen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2020 Published by Elsevier Ltd.en_US
dc.source.pagenumber238-244en_US
dc.source.volume196en_US
dc.source.journalThrombosis Researchen_US
dc.identifier.doi10.1016/j.thromres.2020.08.042
dc.identifier.cristin1870200
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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