OBJETIVE: To estimate the cost- effectiveness of Venetoclax + Rituximab (VEN + R) versus ibrutinib in the treatment of Relapsed/Refractory (R/R) Chronic Lymphocytic Leukaemia (CLL), in Argentina from the Social Security perspective." METHODS: A three-state partitioned survival model (including pre-progression, post-progression and death) developed in accordance with the NICE Guide to the Methods of Technology Appraisal and the ISPOR decision modelling guidelines was adapted to Argentina setting. Population inputs are derived from the MURANO trial. Efficacy and safety data for treatments in R/R CLL were obtained from the literature. The cost of medication was based on country level drug prices. Costs of resources used for routine medical attention and the management of adverse events were based on tariffs from social security system of Argentina. Costs were expressed in US dollars ($) (exchange rate 1$ = 37.10 AR$, November 2018). A 30-year time horizon and the Social Security's payer's perspective were assumed. Costs and health outcomes were discounted at 5%. Deterministic and probabilistic sensitivity analyses (PAS) were performed. RESULTS: Over a 30-year time horizon, VEN + R regimen generates a significantly lower total treatment cost in comparison to Ibrutinib (- US dollars ($) 312.679,37). In QALYs the result is higher in VEN + R related to the comparator (5.83 vs. 4.18). These show that VEN + R is a dominant treatment strategy over Ibutrinib in patients with R/R CLL. The univariate sensitivity and scenario analysis confirm the robustness of this result. Likewise, the probabilistic sensitivity analysis shows that there is a 100% probability that VEN + R is a cost-effective strategy against Ibrutinib. CONCLUSIONS: This study shows that in Argentina, VEN+R would be dominant treatment option (better results and lower costs) compared with ibrutinib in R/R CLL patients. Disclosures Elgart: 3eff: Consultancy. Glancszpigel:3eff: Employment. Kanevsky:Abbvie: Employment. Godar:Abbvie: Employment. Touliet:Abbvie: Employment. Albaytero:3eff: Employment.
OBJECTIVE: Most untreated hepatitis C virus (HCV) patients develop chronic infection and severe complications, including death. Direct-acting antivirals in early stages of liver fibrosis reduce complications and healthcare costs. However, therapy is often delayed, and patients in early stages have limited access to effective treatments. We assessed the clinical and economic effect of treating chronic HCV at early versus late stages of disease in Argentina. METHODS: A Markov model of the natural HCV history was used to forecast lifetime liver-related and economic outcomes from social security sector perspective. Healthcare use and transition probabilities were drawn from literature. Demographic characteristics of the patients and treatment attributes were based on data from registrational trials of glecaprevir/pibrentasvir. RESULTS: Lower rates of all hepatic complications and liver-related mortality were predicted when treatment was initiated in mild versus advanced disease. Sustained virologic response rates were similar among all stages. Higher quality-adjusted life years (QALYs) were predicted when treatment was initiated in mild (F0-F1) versus moderate (F2-F3) or advanced (F4) liver disease (11.5, 9.9, and 7.5 QALYs, respectively). Delaying treatment increased long-term total lifetime costs (F4: AR$ 1 437 816; F2-F3: AR$ 967 673; F0-F1: AR$ 954 018; 37.10 AR$=1 USD, Nov 2018 exchange rate) and provided fewer QALYs. CONCLUSIONS: Our study show early treatment was a dominant strategy compared with treatment in advanced stages of liver disease. These results may help health policy makers take actions to reduce health and economic burden of HCV in Argentina.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.