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1.
Clin Transl Oncol ; 13(12): 869-77, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22126730

ABSTRACT

INTRODUCTION Sunitinib, an oral, multitargeted receptor tyrosine kinase inhibitor, delays disease progression, with a median overall survival (OS) of more than 2 years, improves quality of life and is becoming the first-line standard of care for metastatic renal carcinoma (mRCC). PURPOSE To assess the economic value of sunitinib as fi rst-line therapy in mRCC within the Spanish healthcare system. METHODS An adapted Markov model with a 10-year time horizon was used to analyse the cost effectiveness of sunitinib vs. sorafenib (SFN) and bevacizumab/interferon-α (BEV/IFN) as first-line mRCC therapy from the Spanish third-party payer perspective. Progression-free survival (PFS) and OS data from sunitinib, SFN and BEV/IFN pivotal trials were extrapolated to project survival and costs in 6-week cycles. Results, in progression-free life-years (PFLY), life years (LY) and quality-adjusted life-years (QALY) gained, expressed as incremental cost-effectiveness ratios (ICER) with costs and benefits discounted annually at 3%, were obtained using deterministic and probabilistic analyses. RESULTS Sunitinib was more effective and less costly than both SFN (gains of 0.52 PFLY, 0.16 LY, 0.17 QALY) and BEV/IFN (gains of 0.19 PFLY, 0.23 LY, 0.16 QALY) with average cost savings/patients of €1,124 and €23,218, respectively. Using a willingness-to-pay (WTP) threshold of €50,000/QALY, sunitinib achieved an incremental net benefit (INB) of €9,717 and €31,211 compared with SFN and BEV/IFN, respectively. At this WTP, the probability of sunitinib providing the highest INB was 75%. CONCLUSION Our analysis suggests that sunitinib is a costeffective alternative to other targeted therapies as first-line mRCC therapy in the Spanish healthcare setting.


Subject(s)
Angiogenesis Inhibitors/economics , Carcinoma, Renal Cell/economics , Indoles/economics , Kidney Neoplasms/economics , Models, Economic , Pyrroles/economics , Angiogenesis Inhibitors/therapeutic use , Antiviral Agents/economics , Antiviral Agents/therapeutic use , Benzenesulfonates/economics , Benzenesulfonates/therapeutic use , Carcinoma, Renal Cell/drug therapy , Carcinoma, Renal Cell/secondary , Clinical Trials as Topic , Cost-Benefit Analysis , Humans , Indoles/therapeutic use , Interferon-alpha/economics , Interferon-alpha/therapeutic use , Kidney Neoplasms/drug therapy , Kidney Neoplasms/pathology , Markov Chains , Niacinamide/analogs & derivatives , Phenylurea Compounds , Protein Kinase Inhibitors/economics , Protein Kinase Inhibitors/therapeutic use , Pyridines/economics , Pyridines/therapeutic use , Pyrroles/therapeutic use , Quality-Adjusted Life Years , Sorafenib , Sunitinib
2.
Clin. transl. oncol. (Print) ; 13(12): 869-877, dic. 2011. tab, ilus
Article in English | IBECS | ID: ibc-125995

ABSTRACT

INTRODUCTION Sunitinib, an oral, multitargeted receptor tyrosine kinase inhibitor, delays disease progression, with a median overall survival (OS) of more than 2 years, improves quality of life and is becoming the first-line standard of care for metastatic renal carcinoma (mRCC). PURPOSE To assess the economic value of sunitinib as fi rst-line therapy in mRCC within the Spanish healthcare system. METHODS An adapted Markov model with a 10-year time horizon was used to analyse the cost effectiveness of sunitinib vs. sorafenib (SFN) and bevacizumab/interferon-α (BEV/IFN) as first-line mRCC therapy from the Spanish third-party payer perspective. Progression-free survival (PFS) and OS data from sunitinib, SFN and BEV/IFN pivotal trials were extrapolated to project survival and costs in 6-week cycles. Results, in progression-free life-years (PFLY), life years (LY) and quality-adjusted life-years (QALY) gained, expressed as incremental cost-effectiveness ratios (ICER) with costs and benefits discounted annually at 3%, were obtained using deterministic and probabilistic analyses. RESULTS Sunitinib was more effective and less costly than both SFN (gains of 0.52 PFLY, 0.16 LY, 0.17 QALY) and BEV/IFN (gains of 0.19 PFLY, 0.23 LY, 0.16 QALY) with average cost savings/patients of €1,124 and €23,218, respectively. Using a willingness-to-pay (WTP) threshold of €50,000/QALY, sunitinib achieved an incremental net benefit (INB) of €9,717 and €31,211 compared with SFN and BEV/IFN, respectively. At this WTP, the probability of sunitinib providing the highest INB was 75%. CONCLUSION Our analysis suggests that sunitinib is a costeffective alternative to other targeted therapies as first-line mRCC therapy in the Spanish healthcare setting (AU)


Subject(s)
Humans , Male , Female , Angiogenesis Inhibitors/economics , Carcinoma, Renal Cell/economics , Clinical Trials as Topic/methods , Indoles/economics , Indoles/therapeutic use , Interferon-alpha/economics , Kidney Neoplasms/economics , Kidney Neoplasms/pathology , Models, Economic , Pyrroles/economics , Angiogenesis Inhibitors/therapeutic use , Antiviral Agents/economics , Pyrroles/therapeutic use , Antiviral Agents/therapeutic use , Benzenesulfonates/economics , Benzenesulfonates/therapeutic use , Carcinoma, Renal Cell/drug therapy , Carcinoma, Renal Cell/secondary , Costs and Cost Analysis
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