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https://ahro.austin.org.au/austinjspui/handle/1/16992
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DC Field | Value | Language |
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dc.contributor.author | Petrella, Teresa M | - |
dc.contributor.author | Robert, Caroline | - |
dc.contributor.author | Richtig, Erika | - |
dc.contributor.author | Miller, Wilson H Jr | - |
dc.contributor.author | Masucci, Giuseppe V | - |
dc.contributor.author | Walpole, Euan | - |
dc.contributor.author | Lebbe, Celeste | - |
dc.contributor.author | Steven, Neil | - |
dc.contributor.author | Middleton, Mark R | - |
dc.contributor.author | Hille, Darcy | - |
dc.contributor.author | Zhou, Wei | - |
dc.contributor.author | Ibrahim, Nageatte | - |
dc.contributor.author | Cebon, Jonathan S | - |
dc.date | 2017-10-04 | - |
dc.date.accessioned | 2017-12-08T03:10:44Z | - |
dc.date.available | 2017-12-08T03:10:44Z | - |
dc.date.issued | 2017-11 | - |
dc.identifier.citation | European Journal of Cancer 2017; 86: 115-124 | en_US |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/16992 | - |
dc.description.abstract | OBJECTIVE: 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.subject | Advanced melanoma | en_US |
dc.subject | EORTC QLQ-C30 | en_US |
dc.subject | Health-related quality of life | en_US |
dc.subject | KEYNOTE-006 | en_US |
dc.subject | Patient-reported outcomes | en_US |
dc.subject | Pembrolizumab | en_US |
dc.title | Patient-reported outcomes in KEYNOTE-006, a randomised study of pembrolizumab versus ipilimumab in patients with advanced melanoma | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | European Journal of Cancer | en_US |
dc.identifier.affiliation | Sunnybrook Health Sciences Centre, University of Toronto, Toronto, ON, Canada | en_US |
dc.identifier.affiliation | Gustave Roussy and Université Paris-Sud, France | en_US |
dc.identifier.affiliation | Medical University of Graz, Graz, Austria | en_US |
dc.identifier.affiliation | Segal Cancer Centre, Jewish General Hospital, Rossy Cancer Network, and McGill University, Montreal, QC, Canada | en_US |
dc.identifier.affiliation | Karolinska Institute, Stockholm, Sweden | en_US |
dc.identifier.affiliation | Princess Alexandra Hospital and The University of Queensland, Woolloongabba, Brisbane, Queensland, Australia | en_US |
dc.identifier.affiliation | APHP, Dermatology and CIC, Université Paris Diderot, Hôpital Saint-Louis, Paris, France | en_US |
dc.identifier.affiliation | Queen Elizabeth Hospital Birmingham, Mindelsohn Way, Birmingham, UK | en_US |
dc.identifier.affiliation | The Churchill Hospital and The University of Oxford, Old Rd, Headington, Oxford, UK | en_US |
dc.identifier.affiliation | Merck & Co., Inc., Kenilworth, NJ, USA | en_US |
dc.identifier.affiliation | Olivia Newton-John Cancer Research Institute, Austin Health, School of Cancer Medicine, La Trobe University, Heidelberg, Victoria, Australia | en_US |
dc.identifier.pubmeduri | https://pubmed.ncbi.nlm.nih.gov/28987768 | en_US |
dc.identifier.doi | 10.1016/j.ejca.2017.08.032 | en_US |
dc.type.content | Text | en_US |
dc.type.austin | Journal Article | en_US |
local.name.researcher | Cebon, Jonathan S | |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
Appears in Collections: | Journal articles |
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