Author(s)
Chaker O1, Nucit A2, Salvignol O3, Thoren AC3, Cranmer H4, Coulibaly C3, Chevalier J1, Borget I5
1VYOO Agency, Paris, 75, France, 2Takeda France, Paris, France, 3Takeda France, Paris, 75, France, 4Takeda Pharmaceuticals International Co., London, UK, 5Department of Biostatistics and Epidemiology, Gustave Roussy, Paris-Saclay University, Villejuif, France; Oncostat; GRADES, Paris-Saclay University, Châtenay-Malabry, France U1018, Inserm, Paris-Saclay University, “Ligue Contre le Cancer” labeled team, Chatenay-Malabry, 92, France
OBJECTIVES Systemic anaplastic large cell lymphoma (sALCL) is a rare type of non-Hodgkin lymphoma and one of the subtypes of peripheral T-cell lymphoma. The objective of this study was to estimate the cost-effectiveness of brentuximab vedotin (BV) in combination with cyclophosphamide, doxorubicin and prednisone (CHP) chemotherapy versus current chemotherapies in France. METHODS A cost-effectiveness analysis was developed using a three-state partitioned survival model (progression-free survival, post-progression survival, death) over a lifetime (35-year) horizon to compare BV+CHP to chemotherapies from a collective perspective. The simulated population and the clinical effectiveness for BV+CHP were based on the pivotal clinical trial ECHELON-2 results. The main comparator included in this analysis was cyclophosphamide, doxorubicin, etoposide, vincristine and prednisone (CHOEP) chemotherapy with relative efficacy/effectiveness and safety data derived from a network meta-analysis. Costs were measured in 2020 euros and effects measured in quality-adjusted life years (QALYs). These were evaluated with a discount rate of 2.5% and 1.5% per annum before and after 30-years, respectively, according to French guidelines. Uncertainty associated to methodological assumptions and model parameters was addressed through scenario analyses and deterministic/probabilistic sensitivity analyses. RESULTS Over a lifetime horizon, the regimen of BV+CHP versus CHOEP was associated with 3.6 QALYs gained at a total incremental cost of 43 844€, resulting in an incremental cost-effectiveness ratio (ICER) of approximately 12 211€. According to overall survival extrapolation, BV+CHP was associated with an extension of 4.4 life years. The probabilistic sensitivity analyses generated a 95%CI of [0€ ; 40 900€] and an 80% probability of being cost-effective based on a willingness to pay (WTP) of 19 000€/QALY. CONCLUSIONS The regimen of BV+CHP is estimated to improve life expectancy by 4.4 years over a lifetime horizon and is likely to be cost-effective in France, with an ICER of 12 211€, based on conventional WTP threshold in patients suffering from sALCL.
Conference/Value in Health Info
2021-11, ISPOR Europe 2021, Copenhagen, Denmark
Value in Health, Volume 24, Issue 12, S2 (December 2021)
Code
POSC49
Topic
Economic Evaluation
Topic Subcategory
Cost-comparison, Effectiveness, Utility, Benefit Analysis
Disease
Drugs, Oncology