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dc.contributor.authorSjøgren, Kristina
dc.contributor.authorJacobsen, Kristian Aalberg
dc.contributor.authorGrønberg, Bjørn Henning
dc.contributor.authorHalvorsen, Tarje Onsøien
dc.date.accessioned2021-10-25T08:10:48Z
dc.date.available2021-10-25T08:10:48Z
dc.date.created2020-12-15T12:54:29Z
dc.date.issued2020
dc.identifier.citationAnticancer Research. 2020, 40 (11), 6399-6406.en_US
dc.identifier.issn0250-7005
dc.identifier.urihttps://hdl.handle.net/11250/2825192
dc.description.abstractBackground/Aim: The aim of this study was to investigate the timing of severe toxicity in lung cancer patients receiving chemotherapy. Patients and Methods: Patients with advanced non-small cell lung cancer or limited disease small cell lung cancer included in two randomized controlled trials were analysed. Severe toxicity was defined as grade 3-5 toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) v3.0. Results: We analysed 569 patients and 433 (76.1%) experienced severe toxicity. Of these, 249 (57.5%) experienced the first episode of severe toxicity after the first, 109 (25.2%) after the second, 54 (12.5%) after the third and 18 (4.2%) after the fourth course of chemotherapy. Performance status (PS 2 vs. 0-1; p=0.046) and treatment arm were independent predictive factors for severe toxicity. Conclusion: Severe toxicity was most frequent after the first chemotherapy course, but some patients did not experience severe toxicity until after the fourth course. Accounting for timing might be important when studying factors predicting severe toxicity.en_US
dc.language.isoengen_US
dc.publisherInternational Institute of Anticancer Researchen_US
dc.titleTiming of severe toxicity from chemotherapy in patients with lung canceren_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionacceptedVersionen_US
dc.rights.holderCopyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserveden_US
dc.source.pagenumber6399-6406en_US
dc.source.volume40en_US
dc.source.journalAnticancer Researchen_US
dc.source.issue11en_US
dc.identifier.doi10.21873/anticanres.14661
dc.identifier.cristin1860019
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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