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dc.contributor.authorValan, Christine Damgaard
dc.contributor.authorSlagsvold, Jens Erik
dc.contributor.authorHalvorsen, Tarje Onsøien
dc.contributor.authorHerje, Martin
dc.contributor.authorBremnes, Roy M.
dc.contributor.authorBrunsvig, Paal Fr.
dc.contributor.authorBrustugun, Odd Terje
dc.contributor.authorFløtten, Øystein
dc.contributor.authorLevin, Nina
dc.contributor.authorSundstrøm, Stein Harald
dc.contributor.authorGrønberg, Bjørn Henning
dc.date.accessioned2018-05-07T07:54:29Z
dc.date.available2018-05-07T07:54:29Z
dc.date.created2018-01-18T00:57:32Z
dc.date.issued2018
dc.identifier.issn0250-7005
dc.identifier.urihttp://hdl.handle.net/11250/2497271
dc.description.abstractBackground/Aim: There are several definitions of limited disease (LD) in small cell lung cancer (SCLC), differing with respect to N3 disease accepted. We analyzed patients from a randomized trial comparing two schedules of thoracic radiotherapy (TRT) in LD SCLC to investigate whether there were survival differences between N3 subcategories (n=144). Patients and Methods: Patients with a baseline CT scan available were analysed. Patients received four courses of cisplatin/etoposide and TRT of 45 Gy/30 fractions (twice daily) or 42 Gy/15 fractions (once daily). Results: Median overall survival (OS) was 23.3 months in the whole cohort. N3-patients (n=37) had shorter survival than those with N0-2 (16.7 vs. 33.0 months; p<0.001). There were no significant OS-differences between the N3 subcategories, but patients with metastases to two or more N3 regions had shorter survival than other N3 patients (13.4 vs. 19.9 months; p=0.011). Conclusion: There were no survival differences between the N3 subcategories, suggesting that all N3 disease should be considered as LD.nb_NO
dc.language.isoengnb_NO
dc.publisherInternational Institute of Anticancer Research (IIAR)nb_NO
dc.titleSurvival in Limited Disease Small Cell Lung Cancer According to N3 Lymph Node Involvementnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber871-876nb_NO
dc.source.volume38nb_NO
dc.source.journalAnticancer Researchnb_NO
dc.source.issue2nb_NO
dc.identifier.doi10.21873/anticanres.12296
dc.identifier.cristin1545898
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2017 by International Institute of Anticancer Research (IIAR)nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedfalse
cristin.fulltextpostprint
cristin.qualitycode1


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