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dc.contributor.authorWoods, BS
dc.contributor.authorSideris, E
dc.contributor.authorSydes, MR
dc.contributor.authorGannon, MR
dc.contributor.authorParmar, MKB
dc.contributor.authorAlzouebi, M
dc.contributor.authorAttard, G
dc.contributor.authorBirtle, AJ
dc.contributor.authorBrock, S
dc.contributor.authorCathomas, R
dc.contributor.authorChakraborti, PR
dc.contributor.authorCook, A
dc.contributor.authorCross, WR
dc.contributor.authorDearnaley, DP
dc.contributor.authorGale, J
dc.contributor.authorGibbs, S
dc.contributor.authorGraham, JD
dc.contributor.authorHughes, R
dc.contributor.authorJones, RJ
dc.contributor.authorLaing, R
dc.contributor.authorMason, MD
dc.contributor.authorMatheson, D
dc.contributor.authorMcLaren, DB
dc.contributor.authorMillman, R
dc.contributor.authorO'Sullivan, JM
dc.contributor.authorParikh, O
dc.contributor.authorParker, CC
dc.contributor.authorPeedell, C
dc.contributor.authorProtheroe, A
dc.contributor.authorRitchie, AWS
dc.contributor.authorRobinson, A
dc.contributor.authorRussell, JM
dc.contributor.authorSimms, MS
dc.contributor.authorSrihari, NN
dc.contributor.authorSrinivasan, R
dc.contributor.authorStaffurth, JN
dc.contributor.authorSundar, S
dc.contributor.authorThalmann, GN
dc.contributor.authorTolan, S
dc.contributor.authorTran, ATH
dc.contributor.authorTsang, D
dc.contributor.authorWagstaff, J
dc.contributor.authorJames, ND
dc.contributor.authorSculpher, MJ
dc.date.accessioned2019-06-24T08:50:27Z
dc.date.issued2018-12-01
dc.identifier.citationEuropean urology oncology, 2018, 1 (6), pp. 449 - 458
dc.identifier.issn2588-9311
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3267
dc.identifier.eissn2588-9311
dc.identifier.doi10.1016/j.euo.2018.06.004
dc.description.abstractBACKGROUND: Results from large randomised controlled trials have shown that adding docetaxel to the standard of care (SOC) for men initiating hormone therapy for prostate cancer (PC) prolongs survival for those with metastatic disease and prolongs failure-free survival for those without. To date there has been no formal assessment of whether funding docetaxel in this setting represents an appropriate use of UK National Health Service (NHS) resources. OBJECTIVE: To assess whether administering docetaxel to men with PC starting long-term hormone therapy is cost-effective in a UK setting. DESIGN, SETTING, AND PARTICIPANTS: We modelled health outcomes and costs in the UK NHS using data collected within the STAMPEDE trial, which enrolled men with high-risk, locally advanced metastatic or recurrent PC starting first-line hormone therapy. INTERVENTION: SOC was hormone therapy for ≥2 yr and radiotherapy in some patients. Docetaxel (75mg/m2) was administered alongside SOC for six three-weekly cycles. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The model generated lifetime predictions of costs, changes in survival duration, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICERs). RESULTS AND LIMITATIONS: The model predicted that docetaxel would extend survival (discounted quality-adjusted survival) by 0.89 yr (0.51) for metastatic PC and 0.78 yr (0.39) for nonmetastatic PC, and would be cost-effective in metastatic PC (ICER £5514/QALY vs SOC) and nonmetastatic PC (higher QALYs, lower costs vs SOC). Docetaxel remained cost-effective in nonmetastatic PC when the assumption of no survival advantage was modelled. CONCLUSIONS: Docetaxel is cost-effective among patients with nonmetastatic and metastatic PC in a UK setting. Clinicians should consider whether the evidence is now sufficiently compelling to support docetaxel use in patients with nonmetastatic PC, as the opportunity to offer docetaxel at hormone therapy initiation will be missed for some patients by the time more mature survival data are available. PATIENT SUMMARY: Starting docetaxel chemotherapy alongside hormone therapy represents a good use of UK National Health Service resources for patients with prostate cancer that is high risk or has spread to other parts of the body.
dc.formatPrint-Electronic
dc.format.extent449 - 458
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectProstatic Neoplasms
dc.subjectNeoplasm Recurrence, Local
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectPrognosis
dc.subjectQuality-Adjusted Life Years
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectCost-Benefit Analysis
dc.subjectMale
dc.subjectStandard of Care
dc.subjectUnited Kingdom
dc.subjectDocetaxel
dc.titleAddition of Docetaxel to First-line Long-term Hormone Therapy in Prostate Cancer (STAMPEDE): Modelling to Estimate Long-term Survival, Quality-adjusted Survival, and Cost-effectiveness.
dc.typeJournal Article
dcterms.dateAccepted2018-06-12
rioxxterms.versionofrecord10.1016/j.euo.2018.06.004
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfEuropean urology oncology
pubs.issue6
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Prostate and Bladder Cancer Research
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Prostate and Bladder Cancer Research
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume1
pubs.embargo.termsNot known
icr.researchteamClinical Academic Radiotherapy (Dearnaley)
icr.researchteamProstate and Bladder Cancer Research
dc.contributor.icrauthorDearnaley, David
dc.contributor.icrauthorJames, Nicholas


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