Cost-Effectiveness Analysis of Brentuximab Vedotin in Combination With Doxorubicin, Vinblastine and Dacarbazine (AVD) in Newly Diagnosed Stage III Hodgkin Lymphoma in Italy

Author(s)

Marcellusi A1, Bini C2, Ripoli S3, Fioravanti L3, Molinari A4, Morelli P3, Krotneva M5, Li S6, Paly V7
1Economic Evaluation and HTA (EEHTA CEIS), Department of Economics and Finance, Faculty of Economics, University of Rome “Tor Vergata”, Rome, Italy, 2Economic Evaluation and HTA (EEHTA CEIS), Department of Economics and Finance, Faculty of Economics, University of Rome “Tor Vergata”, Roma, RM, Italy, 3Takeda, Rome, Italy, 4Takeda Pharmaceuticals, Charlestown, MA, USA, 5Evidera, Toronto, ON, Canada, 6Evidera, Waltham, MA, USA, Waltham, MA, USA, 7Takeda Pharmaceuticals America, Inc., Cambridge, MA, USA

OBJECTIVES: Advanced Hodgkin's lymphoma (HL) is a rare severe neoplasm that particularly affects young adults of working age and older people significantly limiting their ability to carry out daily activities. Advanced stage disease at diagnosis is seen in about 40% of patients, and outcomes are historically less favourable in these patients. Classically, first-line treatment with doxorubicin (Adriamycin), bleomycin, vinblastine, and dacarbazine (ABVD) has been the standard of care in advanced stage classic Hodgkin’s lymphoma. Nevertheless, a considerable proportion of patients with stage III/IV disease relapse and/or become refractory to ABVD therapy. This analysis investigates the cost-effectiveness of brentuximab vedotin in combination with AVD (A+AVD) versus ABVD for the treatment of stage III Hodgkin’s lymphoma in Italy, the most recent indication approved by EMA on 12 October 2023.

METHODS: The analysis was conducted from the National Health Service (NHS) perspective using as a Markov model structure with three mutually exclusive health states, weekly cycles, and a lifetime time horizon. Transition probabilities were derived from the ECHELON-1 six-year survival data. Cost inputs were obtained mainly from published literature and national tariffs. Costs, life years (LYs) and quality-adjusted life years (QALYs) were discounted by 3%. Deterministic and probabilistic sensitivity analyses were conducted to handle uncertainty of the model parameters.

RESULTS: A+AVD was associated with a total cost increase of € 25,523, as well as an incremental 0.75 LYs and 0.62 QALYs gained compared with ABVD. Thus, the incremental cost-effectiveness ratio and the incremental cost-utility ratio were estimated l to be € 34,162/LY and € 41,095/QALY respectively.

CONCLUSIONS: Considering the national willingness-to-pay threshold observed in Italy for a more severe disease is € 41,411 per QALY gained, A+AVD can be considered a cost-effective treatment option compared to ABVD for the treatment of patients with stage III HL.

Conference/Value in Health Info

2024-11, ISPOR Europe 2024, Barcelona, Spain

Value in Health, Volume 27, Issue 12, S2 (December 2024)

Code

EE550

Topic

Economic Evaluation

Topic Subcategory

Cost-comparison, Effectiveness, Utility, Benefit Analysis

Disease

Drugs, Oncology

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