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dc.contributor.authorSingh, Johnny Joginder
dc.contributor.authorStensvold, Andreas
dc.contributor.authorTurzer, Martin
dc.contributor.authorGrov, Ellen Karine
dc.date.accessioned2024-05-16T05:49:58Z
dc.date.available2024-05-16T05:49:58Z
dc.date.created2024-05-15T13:41:25Z
dc.date.issued2024
dc.identifier.citationActa Oncologica. 2024, 63 (May 8), 313-321.en_US
dc.identifier.issn0284-186X
dc.identifier.urihttps://hdl.handle.net/11250/3130622
dc.description.abstractBackground: A significant proportion of patients with incurable cancer receive systemic anticancer therapy (SACT) within their last 30 days of life (DOL). The treatment has questionable benefit, nevertheless is considered a quality indicator of end-of-life (EOL) care. This retrospective cohort study aims to investigate the rates and potential predictors of SACT and factors associated with SACT within the last 30 DOL. The study also evaluates the scope of Eastern Cooperative Oncology Group (ECOG) performance status and the modified Glasgow prognostic score (mGPS) as decision-making tools for oncologists. Patients and material: This review of medical records included 383 patients with non-curable cancer who died between July 2018 and December 2019. Descriptive statistics with Chi-squared tests and regression analysis were used to identify factors associated with SACT within the last 30 DOL. Results: Fifty-seven (15%) patients received SACT within the last 30 DOL. SACT within 30 last DOL was associated with shorter time from diagnosis until death (median 234 days vs. 482, p = 0.008) and ECOG scoreen_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectAnticancermidleren_US
dc.subjectDrugs against canceren_US
dc.subjectPalliasjonen_US
dc.subjectPalliative careen_US
dc.subjectKvalitetsindikatoren_US
dc.subjectQuality indicatoren_US
dc.titleAnticancer therapy at end-of-life: A retrospective cohort studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.2340/1651-226X.2024.22139
dc.identifier.cristin2268906
dc.source.journalActa Oncologicaen_US
dc.source.volume63en_US
dc.source.issueMay 8en_US
dc.source.pagenumber313-321en_US
dc.relation.projectSykehuset Østfold HF: Stensvolden_US
dc.subject.nsiVDP::Andre klinisk medisinske fag: 799en_US
dc.subject.nsiVDP::Other clinical medical sciences: 799en_US


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