Economic Impact of Treatment Sequences for Chronic Lymphocytic Leukemia (CLL) and Budget Impact Analysis of Venetoclax Plus Obinutuzumab Sequences for CLL Patients Not Eligible for Full Dose Fludarabine in France

Background: Venetoclax is an oral small-molecule BCL-2 inhibitor, used in combination with rituximab (V+R) or as a monotherapy in adult patients with relapsed or refractory chronic lymphocytic leukemia (CLL). Venetoclax in combination with obinutuzumab (V+G) for a fixed duration was recently approved by the European Medicines Agency for the management of previously untreated patients with CLL. With multiple additional therapies available for CLL including novel agents such as ibrutinib, Idelalisib + R (Ide+R) and acalabrutinib +/-G, treatment sequences that present the most favorable economic profiles remain unknown. Objective: To estimate the total cumulative costs per patient of different treatment sequences for adult patients with CLL, and to evaluate the budget impact of introducing sequences with V+G in the first line in France. Methods: A partitioned survival model was developed to assess the outcomes of treatment sequences commonly used in France up to three lines of therapy in CLL patients. The target population was previously untreated adult patients with CLL and ineligible for full-dose fludarabine treatment, with or without 17p deletion. The model adopted a French payer perspective with a 10-year time horizon. Patients were distributed into four states in each year: first line, second line, third line therapy, and death. The distribution of patients in each state were determined based on progression-free survival (PFS) and overall survival (OS) estimates for the first two lines of therapy reported in pivotal clinical trials. Other model inputs included treatment costs, monitoring and terminal care costs, transportation costs, tumor lysis syndrome (TLS) prevention costs for venetoclax-based therapies, and costs associated with adverse events (AEs). Additional inputs for the budget impact analysis (BIA) included published epidemiological estimates for patient numbers and proportions of patients receiving each treatment before and after introduction of first-line V+G in the treatment sequence. Patients were treated until progression or maximum duration specified on the label. PFS and OS from trials were extrapolated using an exponential distribution. Model outputs included total cumulative costs per patient, stratified by cost component for each treatment sequence. Results from the BIA included the total budget impact comparing before and after introduction of first line treatment with V+G in France. Results: In patients with 17p deletion, the trea