ReviewDermatology and therapy2026
Comparative Data on Long-Term Efficacy of Biologics in Moderate-to-Severe AD: An Expert Perspective on Using Indirect Comparison Methodology.
Review in Dermatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
- Erratum issued
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionAtopic dermatitis (AD) is a chronic inflammatory skin condition that often requires long-term therapy for effective management. Several biologics have been approved for treating patients with moderate-to-severe AD, but, to date, no head-to-head trials comparing these biologics have been completed. Although long-term data from individual trials have been published, the differences in trial design prevent direct comparisons across treatments and therefore only indirect comparisons, such as matching-adjusted indirect comparisons (MAICs), should be used to compare efficacy endpoints. MAICs utilize individual patient data from one trial, adjusted to match the summary statistics for relevant demographic and disease characteristics with those of an aggregate comparator trial.
methodsAvailable published phase 3 clinical trial data on the long-term efficacy of approved biologics for the treatment of moderate-to-severe AD were reviewed to provide an overview of the key differences in trial design for AD biologics, and the implications of these differences for comparing efficacy. Available published MAIC analyses of clinical trial data were reviewed to provide further insights into the long-term efficacy of approved biologics for the treatment of moderate-to-severe AD.
resultsSix long-term combination therapy and monotherapy trials were summarized and assessed, revealing substantial differences in trial design that prevent efficacy comparisons of AD biologics. Three available MAIC analyses comparing trials of biologics for AD were reviewed and critically assessed, revealing important considerations for robust MAIC analyses and highlighting the limitations and advantages of MAIC analyses in the absence of head-to-head trial data.
conclusionAlthough any interpretation of indirect treatment comparisons should be made with caution, anchored MAIC remains a valuable and methodologically appropriate tool for comparative assessment when direct head-to-head evidence is unavailable. Available MAIC analyses indicate comparable long-term efficacy among three widely-used biologics-tralokinumab, dupilumab, and lebrikizumab-in the treatment of moderate-to-severe AD.
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