Cost-utility of tofacitinib in the treatment of moderate-to-severe rheumatoid arthritis in France: a multi-state Markov model analysis.

Clin Exp Rheumatol

T-RAIG, TIMC, UMR 5525 CNRS, Univ. Grenoble Alpes, CHU Grenoble Alpes, Grenoble, and Department of Rheumatology, CHU Grenoble Alpes, Grenoble, France.

Published: October 2024

AI Article Synopsis

  • The study evaluates the cost-effectiveness of tofacitinib as a second-line treatment after methotrexate failure for rheumatoid arthritis in France using a Markov model with 10,000 simulated patients.
  • Introducing tofacitinib demonstrates cost savings of €1,679 per patient and increases quality-adjusted life years (QALYs) by 0.29 compared to traditional biologic treatments.
  • This research is the first of its kind in France and agrees with findings from other countries, though it acknowledges limitations related to clinical trial data and focuses only on severe adverse effects.

Article Abstract

Objectives: This study aimed to evaluate the cost-effectiveness of introducing tofacitinib in second-line therapies after methotrexate failure for rheumatoid arthritis in France.

Methods: Using a Markov model, we simulated a cohort of 10,000 patients based on literature data to compare various treatment strategies. The reference strategy included the four classes of biologics commonly used in France (TNFi, tocilizumab, abatacept, rituximab). The trial strategies additionally included tofacitinib at different introduction positions. The cycle duration was set at 6 months, and the time horizon was a lifetime. The data for severe adverse effects were sourced from the ORAL Surveillance study.

Results: Compared to the reference strategy, introducing tofacitinib is a dominant strategy, regardless of its introduction position. Introducing it as the first-line treatment results in the greatest cost savings (€1,679 per patient) while increasing quality-adjusted life years (QALYs) by 0.29. According to the one-way sensitivity analysis, the discount rate and the cost of TNFi were the two variables that most influenced costs, while the change in HAQ score and the discount rate were the two variables that most influenced QALYs.

Conclusions: Our study represents the first assessment of the cost-effectiveness of tofacitinib in France and incorporates the latest adverse effects reported in the literature. It reinforces previously obtained results from other countries. Our study has some limitations, mainly related to the use of data from clinical trials. Our analysis is limited to severe adverse effects, and their cost is extrapolated from the average hospitalisation cost. The estimated costs are therefore underestimated for chronic diseases such as cancer.

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Source
http://dx.doi.org/10.55563/clinexprheumatol/3f60yvDOI Listing

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