Hicks K, Earnshaw S, McDade C, Shaw JW, Cifaldi MA. Benefit-risk analysis of adalimumab and alternative treatments for moderate to severe rheumatoid arthritis. Poster presented at the 2012 ISPOR 15th Annual European Congress; November 13, 2012. Berlin, Germany. [abstract] Value Health. 2012 Nov; 15(7):A439-40.


OBJECTIVES: To compare treatment-related risks versus improvements in outcomes in terms of net health benefit (NHB) for 3 treatments for moderate-to-severe rheumatoid arthritis: the anti–tumor necrosis factor drugs (anti-TNFs) adalimumab (ADA) and infliximab (IFX), both in combination with methotrexate (MTX), and MTX alone.

METHODS: A simulation model was developed in which a cohort of rheumatoid arthritis patients initiating treatment progressed at 6-month intervals for 10 years or until withdrawal from therapy. NHB, measured in discounted quality-adjusted life-years (QALYs), was calculated for patients receiving ADAMTX, IFXMTX, and MTX alone. Outcomes were examined separately for MTX-naïve and disease-modifying antirheumatic drug (DMARD)–failure patients. Treatment benefits were measured by American College of Rheumatology 20, 50, and 70 responses and translated into improvements in Health Assessment Questionnaire Disability Index scores. Risks comprised loss of drug efficacy and adverse events; patients could withdraw from treatment due to either. Benefits and risks were associated with increments and decrements in QALYs, respectively. Data were derived from the published literature and drug prescribing information.

RESULTS: MTX-naive patients on ADAMTX, IFXMTX, and MTX alone withdrew after 3.31, 2.46, and 2.71 years and accrued NHBs of 1.40, 1.05, and 1.08 QALYs, respectively. Thus, MTX-naive patients on ADAMTX accrued incremental NHBs of 0.35 (P .05) versus IFXMTX and 0.32 (P .05) versus MTX alone. DMARD-failure patients on ADAMTX, IFXMTX, and MTX alone withdrew after 3.33, 2.11, and 1.44 years and accrued NHBs of 1.38, 0.86, and 0.57 QALYs, respectively. Thus, DMARD-failure patients on ADAMTX incurred incremental NHBs of 0.51 (P.05) versus IFXMTX and 0.81 (P .05) versus MTX alone.

CONCLUSIONS: Understanding the benefit-risk tradeoff is important for clinicians when prescribing anti-TNFs. Both MTX naive and DMARD-failure patients may experience greater NHB when treated with ADAMTX than when treated with IFXMTX or MTX alone.

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