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Cost-Effectiveness of Biosimilars vs Leflunomide

An economic evaluation of 25 099 rheumatoid arthritis patients found that treatment with biosimilar disease-modifying antirheumatic drugs (DMARDs) were cost-effective compared with the conventional DMARD, leflunomide. Does this suggest RA treatment guidelines need to be amended to allow biosimilars use immediately after the failure of methotrexate?

A cost-effectiveness analysis was performed using Hong Kong public electronic medical record data and a Markov disease transition model to simulate the lifetime disease progression and cost for patients with RA, using monetary valuesf rom 2022. The model assessed 3 competing treatment sequences initiated with biosimilar infliximab (CT-P13), biosimilar adalimumab (ABP-501), and leflunomide; all used in combination with methotrexate. The primary outcome was health care cost and quality-adjusted life-years (QALYs) of the simulated cohort.

From a total of 25 099 RA patients (mean age 56 years, 73% women), the lifetime health care cost and QALYs per treatment sequence initiated with:

  • Leflunomide - US $154 632 and 14.82 QALYs
  • Biosimilar infliximab (CT-P13) - US $152 326 and 15.35 QALYs
  • Biosimilar adalimumab (aBP-501) - US $145 419 and 15.55 QALYs

Both biosimilar choices presented lower costs and greater QALYs than the leflunomide choice. The incremental cost-effectiveness ratio (US$/QALY) comparing biosimilar infliximab sequence vs leflunomide sequence and biosimilar adalimumab sequence vs leflunomide sequence ranged from −15 797 to −8615 and −9088 to 10 238, respectively (all below the predefined willingness-to-pay threshold of US $48 555/QALY gain). 

Treatment initiated with biosimilar DMARDs were cost-effective compared with leflunomide in managing RA patients not responding to an initial methotrexate treatment. Cost-effective biosimilars need not be reserved for late stage, 3rd or 4th line treatment in RA.  

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Disclosures
The author has no conflicts of interest to disclose related to this subject