Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/8527
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dc.contributor.authorJovan Mihajlovićen_US
dc.contributor.authorPetros Pechlivanoglouen_US
dc.contributor.authorAna Saboen_US
dc.contributor.authorZdenko Tomićen_US
dc.contributor.authorMaarten Postmaen_US
dc.date.accessioned2019-09-30T09:09:20Z-
dc.date.available2019-09-30T09:09:20Z-
dc.date.issued2013-12-01-
dc.identifier.issn1492918en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/8527-
dc.description.abstractBackground: New targeted therapeutics for metastatic renal cell carcinoma (mRCC) enable an increment in progression-free survival (PFS) ranging from 2 to 6 months. Compared with best supportive care, everolimus demonstrated an additional PFS of 3 months in patients with mRCC whose disease had progressed on sunitinib and/or sorafenib. The only targeted therapy for mRCC currently reimbursed in Serbia is sunitinib. Objective: The aim of this study was to estimate the cost-effectiveness and the budget impact of the introduction of everolimus in Serbia in comparison to best supportive care, for mRCC patients refractory to sunitinib. Methods: A Markov model was designed corresponding with Serbian treatment protocols. A health care payer perspective was taken, including direct costs only. Treated and untreated cohorts were followed up over 18 cycles, each cycle lasting 8 weeks, which covered the lifetime horizon of mRCC patients refractory to the first-line treatment. Annual discounted rates of 1.5% for effectiveness and 3% for costs were applied. Transitions between health states were modeled by time-dependent probabilities extracted from published Kaplan-Meier curves of PFS and overall survival (OS). Utility values were obtained from the appraisals of other mRCC treatments. One-way and probabilistic sensitivity analyses were done to test the robustness and uncertainty of the base-case estimate. Lastly, the potential impacts of everolimus on the overall health care expenditures on annual and 4-year bases were estimated in the budget-impact analysis. Results: The incremental cost-effectiveness ratio for everolimus was estimated at €86,978 per quality-adjusted life-year. Sensitivity analysis identified the hazard multiplier, a statistical approximator of OS gain, as the main driver of everolimus cost-effectiveness. Furthermore, probabilistic sensitivity analyses revealed a wide 95% CI around the base-case incremental cost-effectiveness ratio estimate (€32,594-€425,258 per quality-adjusted life-year). Finally, an average annual budgetary impact of everolimus in first 4 years after its potential reimbursement would be around €270,000, contributing to <1% of the total budget in Serbian oncology. Conclusions: Everolimus as a second-line treatment of mRCC is not likely to be a cost-effective option under the present conditions in Serbia, with a relatively limited impact on its budget in oncology. A major constraint on the estimation of the cost-effectiveness of everolimus relates to the uncertainty around the everolimus effect on extending OS. However, prior to a final decision on the acceptance/rejection of everolimus, reassessment of the whole therapeutic group might be needed to construct an economically rational treatment strategy within the mRCC field. © 2013 Elsevier HS Journals, Inc.en_US
dc.language.isoenen_US
dc.relation.ispartofClinical Therapeuticsen_US
dc.subjectcost-effectivenessen_US
dc.subjecteverolimusen_US
dc.subjectrenal cell carcinomaen_US
dc.subjectSerbiaen_US
dc.titleCost-Effectiveness of Everolimus for Second-Line Treatment of Metastatic Renal Cell Carcinoma in Serbiaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1016/j.clinthera.2013.10.004-
dc.identifier.pmid35-
dc.identifier.scopus2-s2.0-84890312245-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84890312245-
dc.description.versionPublisheden_US
dc.relation.lastpage1922en_US
dc.relation.firstpage1909en_US
dc.relation.issue12en_US
dc.relation.volume35en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptMedicinski fakultet, Katedra za farmakologiju i toksikologiju-
crisitem.author.parentorgMedicinski fakultet-
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