Assessing the overall benefit of a medication: cumulative benefit of secukinumab over time in patients with moderate-to-severe plaque psoriasis

Background: Conventional measurements for assessing psoriasis treatment effects capture improvements at fixed, pre-specified timepoints, failing to account for cumulative clinical benefit over time.Objective: Explore the innovative concept of cumulative clinical benefit by examining the effect of secukinumab over 52 weeks in moderate-to-severe psoriasis patients.Methods: Cumulative clinical benefit was determined as the area-under-the-curve of the percentage of responders over 52 weeks (AUC(0-52 wks)), using pooled data from two phase III trials for patients receiving secukinumab (300 or 150mg) or etanercept.Results: Normalized cumulative benefit with secukinumab 300mg, secukinumab 150mg, and etanercept was 74.2%, 63.2%, and 50.5%, respectively, for PASI 75; 58.0%, 42.5%, and 29.5%, respectively, for PASI 90; 32.3%, 18.8%, and 8.7%, respectively, for PASI 100; and 58.3%, 47.9%, and 38.3%, respectively, for DLQI 0/1. 52-week PASI 75 clinical benefit ratios for secukinumab 300 and 150mg versus etanercept were 1.47 and 1.25, respectively; the ratio of the two secukinumab doses was 1.17, favoring 300mg.Limitations:Post hoc analysis.Conclusion: Cumulative clinical benefit estimated by AUC(0-52 wks) is a novel measure for comparing psoriasis treatments. Secukinumab 300mg provides greater cumulative clinical benefit than secukinumab 150mg; both provide greater cumulative benefit than etanercept.