Publication:
Health-related Quality of Life in the Phase III LUME-Colon 1 Study: Comparison and Interpretation of Results From EORTC QLQ-C30 Analyses.

dc.contributor.authorLenz, Heinz-Josef
dc.contributor.authorArgiles, Guillem
dc.contributor.authorYoshino, Takayuki
dc.contributor.authorLonardi, Sara
dc.contributor.authorFalcone, Alfredo
dc.contributor.authorLimón, María Luisa
dc.contributor.authorSobrero, Alberto
dc.contributor.authorHastedt, Claudia
dc.contributor.authorPeil, Barbara
dc.contributor.authorVoss, Florian
dc.contributor.authorGriebsch, Ingolf
dc.contributor.authorVan Cutsem, Eric
dc.date.accessioned2023-02-08T14:39:42Z
dc.date.available2023-02-08T14:39:42Z
dc.date.issued2019-09-04
dc.description.abstractWe used European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) data from the LUME-Colon 1 study to illustrate different methods of statistical analysis for health-related quality of life (HRQoL), and compared the results. Patients were randomized 1:1 to receive nintedanib 200 mg twice daily plus best supportive care (n = 386) or matched placebo plus best supportive care (n = 382). Five methods (mean treatment difference averaged over time, using a mixed-effects growth curve model; mixed-effects models for repeated measurements (MMRM); time-to-deterioration (TTD); status change; and responder analysis) were used to analyze EORTC QLQ-C30 global health status (GHS)/QoL and scores from functional scales. Overall, GHS/QoL and physical functioning deteriorated over time. Mean treatment difference slightly favored nintedanib over placebo for physical functioning (adjusted mean, 2.66; 95% confidence interval [CI], 0.97-4.34) and social functioning (adjusted mean, 2.62; 95% CI, 0.66-4.47). GHS/QoL was numerically better with nintedanib versus placebo (adjusted mean, 1.61; 95% CI, -0.004 to 3.27). MMRM analysis had similar results, with better physical functioning in the nintedanib group at all timepoints. There was no significant delay in GHS/QoL deterioration (10%) and physical functioning (16%) with nintedanib versus placebo (TTD analysis). Status change analysis showed a higher proportion of patients with markedly improved GHS/QoL and physical functioning in the nintedanib versus placebo groups. Responder analysis showed a similar, less pronounced pattern. Analyses of EORTC QLQ-C30 data showed that HRQoL was not impaired by treatment with nintedanib versus placebo. Analysis and interpretation of HRQoL endpoints should consider symptom type and severity and course of disease.
dc.identifier.doi10.1016/j.clcc.2019.08.005
dc.identifier.essn1938-0674
dc.identifier.pmcPMC7505163
dc.identifier.pmid31628043
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505163/pdf
dc.identifier.unpaywallURLhttps://www.clinical-colorectal-cancer.com/article/S1533-0028(18)30525-5/pdf
dc.identifier.urihttp://hdl.handle.net/10668/14978
dc.issue.number4
dc.journal.titleClinical colorectal cancer
dc.journal.titleabbreviationClin Colorectal Cancer
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number269-279.e5
dc.pubmedtypeClinical Trial, Phase III
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeRandomized Controlled Trial
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectHRQoL
dc.subjectMMRM
dc.subjectNintedanib
dc.subjectQoL
dc.subjectTime to deterioration
dc.subject.meshAntineoplastic Agents
dc.subject.meshColonic Neoplasms
dc.subject.meshFollow-Up Studies
dc.subject.meshHumans
dc.subject.meshIndoles
dc.subject.meshPrognosis
dc.subject.meshQuality of Life
dc.subject.meshSickness Impact Profile
dc.subject.meshSurveys and Questionnaires
dc.subject.meshSurvival Rate
dc.titleHealth-related Quality of Life in the Phase III LUME-Colon 1 Study: Comparison and Interpretation of Results From EORTC QLQ-C30 Analyses.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number18
dspace.entity.typePublication

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