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SCOT: a comparison of cost-effectiveness from a large randomised phase III trial of two durations of adjuvant Oxaliplatin combination chemotherapy for colorectal cancer.
Robles-Zurita, José; Boyd, Kathleen A; Briggs, Andrew H; Iveson, Timothy; Kerr, Rachel S; Saunders, Mark P; Cassidy, Jim; Hollander, Niels Henrik; Tabernero, Josep; Segelov, Eva; Glimelius, Bengt; Harkin, Andrea; Allan, Karen; McQueen, John; Pearson, Sarah; Waterston, Ashita; Medley, Louise; Wilson, Charles; Ellis, Richard; Essapen, Sharadah; Dhadda, Amandeep S; Hughes, Rob; Falk, Stephen; Raouf, Sherif; Rees, Charlotte; Olesen, Rene K; Propper, David; Bridgewater, John; Azzabi, Ashraf; Farrugia, David; Webb, Andrew; Cunningham, David; Hickish, Tamas; Weaver, Andrew; Gollins, Simon; Wasan, Harpreet S; Paul, James.
Afiliação
  • Robles-Zurita J; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK. JoseAntonio.Robles-Zurita@glasgow.ac.uk.
  • Boyd KA; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Briggs AH; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Iveson T; Southampton University Hospital NHS Foundation Trust, Southampton, UK.
  • Kerr RS; Department of Oncology, University of Oxford, Oxford, UK.
  • Saunders MP; The Christie Hospital, Manchester, UK.
  • Cassidy J; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • Hollander NH; Zealand University Hospital, Department of Oncology and Palliative Care, RÇ»dmandsengen 5, DK 4700, Naestved, Denmark.
  • Tabernero J; Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Universitat Autònoma de Barcelona, CIBERONC, Barcelona, Spain.
  • Segelov E; Australasian Gastro-Intestinal Trials Group (AGITG) and Monash University and Monash Health, Melbourne, Australia.
  • Glimelius B; University of Uppsala, Uppsala, Sweden.
  • Harkin A; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • Allan K; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • McQueen J; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • Pearson S; Department of Oncology, OCTO, University of Oxford, Oxford, UK.
  • Waterston A; Beatson West of Scotland Cancer Centre, Glasgow, UK.
  • Medley L; Royal United Hospital, Bath, UK.
  • Wilson C; Addenbrookes Hospital, Cambridge, UK.
  • Ellis R; Royal Cornwall Hospitals NHS Trust, Cornwall, UK.
  • Essapen S; St Luke's Cancer Centre, Royal Surrey County Hospital NHS Foundation Trust, Guildford, UK.
  • Dhadda AS; Castle Hill Hospital, Hull, UK.
  • Hughes R; Mount Vernon Cancer Centre, Northwood, UK.
  • Falk S; Bristol Cancer Institute, Bristol, UK.
  • Raouf S; Barking Havering and Redbridge University Hospital NHS Trust, Barking, UK.
  • Rees C; Southampton University Hospital NHS Foundation Trust, Southampton, UK.
  • Olesen RK; Zealand University Hospital, Department of Oncology and Palliative Care, RÇ»dmandsengen 5, DK 4700, Naestved, Denmark.
  • Propper D; Barts Cancer Institute, Queen Mary, University of London, London, UK.
  • Bridgewater J; University College London, London, UK.
  • Azzabi A; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.
  • Farrugia D; Gloucestershire Oncology Centre, Cheltenham General Hospital, Cheltenham, UK.
  • Webb A; Brighton and Sussex University Hospital Trust, Brighton, UK.
  • Cunningham D; Royal Marsden (funded by NIHR BRC at the Royal Marsden), London, UK.
  • Hickish T; Poole Hospital/Bournemouth University, Bournemouth, UK.
  • Weaver A; Churchill Hospital, Oxford University Hospitals Foundation Trust, Oxford, UK.
  • Gollins S; North Wales Cancer Treatment Centre, Rhyl, UK.
  • Wasan HS; Hammersmith Hospital, Imperial College London, London, UK.
  • Paul J; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
Br J Cancer ; 119(11): 1332-1338, 2018 11.
Article em En | MEDLINE | ID: mdl-30420616
ABSTRACT

BACKGROUND:

The Short Course Oncology Therapy (SCOT) study is an international, multicentre, non-inferiority randomised controlled trial assessing the efficacy, toxicity, and cost-effectiveness of 3 months (3 M) versus the usually given 6 months (6 M) of adjuvant chemotherapy in colorectal cancer.

METHODS:

In total, 6088 patients with fully resected high-risk stage II or stage III colorectal cancer were randomised and followed up for 3-8 years. The within-trial cost-effectiveness analysis from a UK health-care perspective is presented using the resource use data, quality of life (EQ-5D-3L), time on treatment (ToT), disease-free survival after treatment (DFS) and overall survival (OS) data. Quality-adjusted partitioned survival analysis and Kaplan-Meier Sample Average Estimator estimated QALYs and costs. Probabilistic sensitivity and subgroup analysis was undertaken.

RESULTS:

The 3 M arm is less costly (-£4881; 95% CI -£6269; -£3492) and entails (non-significant) QALY gains (0.08; 95% CI -0.086; 0.230) due to a better significant quality of life. The net monetary benefit was significantly higher in 3 M under a wide range of monetary values of a QALY. The subgroup analysis found similar results for patients in the CAPOX regimen. However, for the FOLFOX regimen, 3 M had lower QALYs than 6 M (not statistically significant).

CONCLUSIONS:

Overall, 3 M dominates 6 M with no significant detrimental impact on QALYs. The results provide the economic case that a 3 M treatment strategy should be considered a new standard of care.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica / Análise Custo-Benefício / Oxaliplatina Tipo de estudo: Clinical_trials / Health_economic_evaluation Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica / Análise Custo-Benefício / Oxaliplatina Tipo de estudo: Clinical_trials / Health_economic_evaluation Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article