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dc.contributor.authorSolheim, Tora Skeidsvoll
dc.contributor.authorLaird, Barry J
dc.contributor.authorBalstad, Trude Rakel
dc.contributor.authorStene, Guro Birgitte
dc.contributor.authorBye, Asta
dc.contributor.authorJohns, Neil
dc.contributor.authorPettersen, Caroline Hild Hakvåg
dc.contributor.authorFallon, Marie
dc.contributor.authorFayers, Peter
dc.contributor.authorFearon, Kenneth
dc.contributor.authorKaasa, Stein
dc.date.accessioned2018-01-30T13:51:33Z
dc.date.available2018-01-30T13:51:33Z
dc.date.created2017-11-20T11:01:41Z
dc.date.issued2017
dc.identifier.citationJournal of Cachexia, Sarcopenia and Muscle. 2017, 8 778-788.nb_NO
dc.identifier.issn2190-5991
dc.identifier.urihttp://hdl.handle.net/11250/2480735
dc.description.abstractBackground: Cancer cachexia is a syndrome of weight loss (including muscle and fat), anorexia, and decreased physical function. It has been suggested that the optimal treatment for cachexia should be a multimodal intervention. The primary aim of this study was to examine the feasibility and safety of a multimodal intervention (n-3 polyunsaturated fatty acid nutritional supplements, exercise, and anti-inflammatory medication: celecoxib) for cancer cachexia in patients with incurable lung or pancreatic cancer, undergoing chemotherapy. Methods: Patients receiving two cycles of standard chemotherapy were randomized to either the multimodal cachexia intervention or standard care. Primary outcome measures were feasibility assessed by recruitment, attrition, and compliance with intervention (>50% of components in >50% of patients). Key secondary outcomes were change in weight, muscle mass, physical activity, safety, and survival. Results: Three hundred and ninety-nine were screened resulting in 46 patients recruited (11.5%). Twenty five patients were randomized to the treatment and 21 as controls. Forty-one completed the study (attrition rate 11%). Compliance to the individual components of the intervention was 76% for celecoxib, 60% for exercise, and 48% for nutritional supplements. As expected from the sample size, there was no statistically significant effect on physical activity or muscle mass. There were no intervention-related Serious Adverse Events and survival was similar between the groups. Conclusions: A multimodal cachexia intervention is feasible and safe in patients with incurable lung or pancreatic cancer; however, compliance to nutritional supplements was suboptimal. A phase III study is now underway to assess fully the effect of the intervention.nb_NO
dc.language.isoengnb_NO
dc.publisherWiley Open Accessnb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleA randomized phase II feasibility trial of a multimodal intervention for the management of cachexia in lung and pancreatic cancernb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber778-788nb_NO
dc.source.volume8nb_NO
dc.source.journalJournal of Cachexia, Sarcopenia and Musclenb_NO
dc.identifier.doi10.1002/jcsm.12201
dc.identifier.cristin1515951
dc.description.localcode© 2017 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of the Society on Sarcopenia, Cachexia and Wasting Disorders Journal of Cachexia, Sarcopenia and Muscle 2017; 8: 778–788 Published online 14 June 2017 in Wiley Online Library (wileyonlinelibrary.com) DOI: 10.1002/jcsm.12201 This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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