Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16992
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dc.contributor.authorPetrella, Teresa M-
dc.contributor.authorRobert, Caroline-
dc.contributor.authorRichtig, Erika-
dc.contributor.authorMiller, Wilson H Jr-
dc.contributor.authorMasucci, Giuseppe V-
dc.contributor.authorWalpole, Euan-
dc.contributor.authorLebbe, Celeste-
dc.contributor.authorSteven, Neil-
dc.contributor.authorMiddleton, Mark R-
dc.contributor.authorHille, Darcy-
dc.contributor.authorZhou, Wei-
dc.contributor.authorIbrahim, Nageatte-
dc.contributor.authorCebon, Jonathan S-
dc.date2017-10-04-
dc.date.accessioned2017-12-08T03:10:44Z-
dc.date.available2017-12-08T03:10:44Z-
dc.date.issued2017-11-
dc.identifier.citationEuropean Journal of Cancer 2017; 86: 115-124en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16992-
dc.description.abstractOBJECTIVE: Report results of patient-reported health-related quality of life (HRQoL) and symptoms from phase III KEYNOTE-006 study of pembrolizumab versus ipilimumab in patients with ipilimumab-naive advanced melanoma. PATIENTS AND METHODS: Patients received pembrolizumab 10 mg/kg every 2 (Q2W) or every 3 weeks (Q3W) for up to 2 years, or four cycles of ipilimumab 3 mg/kg Q3W. The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire C30 (EORTC QLQ-C30) was administered at baseline and throughout the study. Patient-reported outcome (PRO) analyses were pre-specified exploratory endpoints; the primary PRO assessment was the score change from baseline to week 12 in EORTC QLQ-C30 global health status (GHS)/HRQoL score between the arms using constrained longitudinal data analysis. RESULTS: The PRO analysis population included 776 patients: pembrolizumab Q2W (n = 270); pembrolizumab Q3W (n = 266); ipilimumab (n = 240). Baseline GHS was similar across arms. QLQ-C30 compliance rates at week 12 were 87% (n = 214), 97% (n = 226), and 96% (n = 178), for the pembrolizumab Q2W, pembrolizumab Q3W, and ipilimumab arms, respectively. From baseline to week 12, GHS/HRQoL scores were better maintained with pembrolizumab than with ipilimumab (decrease of -1.9 and -2.5 for pembrolizumab versus -10.0 for ipilimumab; p < 0.001 for each pembrolizumab arm versus ipilimumab). Fewer patients treated with pembrolizumab experienced deterioration in GHS at week 12 (31% for pembrolizumab Q2W; 29% for Q3W and 44% for ipilimumab), with similar trends observed for individual functioning and symptoms scales. CONCLUSIONS: HRQoL was better maintained with pembrolizumab than with ipilimumab in patients with ipilimumab-naive advanced melanoma. CLINICALTRIALS. GOV IDENTIFIER: NCT01866319.en_US
dc.subjectAdvanced melanomaen_US
dc.subjectEORTC QLQ-C30en_US
dc.subjectHealth-related quality of lifeen_US
dc.subjectKEYNOTE-006en_US
dc.subjectPatient-reported outcomesen_US
dc.subjectPembrolizumaben_US
dc.titlePatient-reported outcomes in KEYNOTE-006, a randomised study of pembrolizumab versus ipilimumab in patients with advanced melanomaen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleEuropean Journal of Canceren_US
dc.identifier.affiliationSunnybrook Health Sciences Centre, University of Toronto, Toronto, ON, Canadaen_US
dc.identifier.affiliationGustave Roussy and Université Paris-Sud, Franceen_US
dc.identifier.affiliationMedical University of Graz, Graz, Austriaen_US
dc.identifier.affiliationSegal Cancer Centre, Jewish General Hospital, Rossy Cancer Network, and McGill University, Montreal, QC, Canadaen_US
dc.identifier.affiliationKarolinska Institute, Stockholm, Swedenen_US
dc.identifier.affiliationPrincess Alexandra Hospital and The University of Queensland, Woolloongabba, Brisbane, Queensland, Australiaen_US
dc.identifier.affiliationAPHP, Dermatology and CIC, Université Paris Diderot, Hôpital Saint-Louis, Paris, Franceen_US
dc.identifier.affiliationQueen Elizabeth Hospital Birmingham, Mindelsohn Way, Birmingham, UKen_US
dc.identifier.affiliationThe Churchill Hospital and The University of Oxford, Old Rd, Headington, Oxford, UKen_US
dc.identifier.affiliationMerck & Co., Inc., Kenilworth, NJ, USAen_US
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Austin Health, School of Cancer Medicine, La Trobe University, Heidelberg, Victoria, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28987768en_US
dc.identifier.doi10.1016/j.ejca.2017.08.032en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherCebon, Jonathan S
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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