Background: The evidence base of tisagenlecleucel is uncertain.
Objective: To evaluate the cost-effectiveness of tisagenlecleucel. To conduct expected value of perfect information (EVPI) and partial EVPI (EVPPI) analyses.
Study design: A three-state partitioned survival model. A short-term decision tree partitioned patients in the tisagenlecleucel arm according to infusion status. Survival was extrapolated to 5 years; general population mortality with a standardised mortality ratio was then applied. EVPI and EVPPI were scaled up to population according to the incidence of the decision.
Setting: Irish healthcare payer.
Participants: Patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL).
Interventions: Tisagenlecleucel versus Salvage Chemotherapy (with or without haematopoietic stem cell transplant).
Main outcome measure: Incremental cost-effectiveness ratio (ICER). Population EVPI and EVPPI.
Results: At list prices, the ICER was €119,509 per quality-adjusted life year (QALY) (incremental costs €218,092; incremental QALYs 1.82). Probability of cost-effectiveness, at a €45,000 per QALY threshold, was 0%. Population EVPI was €0.00. Population EVPI, at the price of tisagenlecleucel that reduced the ICER to €45,000 per QALY, was €3,989,438. Here, survival analysis had the highest population EVPPI (€1,128,053).
Conclusion: Tisagenlecleucel is not cost-effective, versus salvage chemotherapy (with or without haematopoietic stem cell transplant), for R/R DLBCL in Ireland. At list prices, further research to decrease decision uncertainty may not be of value.
Keywords: CAR T-cell therapy; Cost-utility analysis; cost-effectiveness; expected value of perfect information; value of information.
© 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.