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◆ Journal of the European Academy of Dermatology and Venereology2025-11-14· Medicine

From reactive to predictive: Advancing biologic dosing in dermatology

Anke Eylenbosch, Ruoheng Wei, Rani Soenen, Catherine Smith, Joseph F. Standing, Satveer K. Mahil, Jo Lambert

原始摘要(英文原文)· Original abstract
Biologic therapies are targeted immunomodulators that have revolutionised the treatment of chronic inflammatory dermatoses, including psoriasis, hidradenitis suppurativa and atopic dermatitis, offering high efficacy and safety for moderate-to-severe disease. However, standardised dosing regimens fail to account for inter-individual heterogeneity, leading to non-optimal drug exposure in certain patients. This may, in part, explain why primary non-response, secondary loss of response or adverse effects are observed in real-world practice. While empirical off-label adjustments are commonly employed, data-driven dosing optimisation may enable better disease control and reduce the burden of lifelong biologic treatment by avoiding excessive dosing. Therapeutic drug monitoring (TDM) involves adjusting doses based on serum drug concentrations to maintain therapeutic ranges, relying on established dose-exposure-response correlations. Although TDM provides reactive or proactive optimisation approaches, its threshold-based adjustments are limited by an inability to predict individual pharmacokinetic variability or future clinical outcomes. Model-informed precision dosing (MIPD) represents an evolution beyond conventional TDM by integrating population pharmacokinetic-pharmacodynamic models, patient-specific characteristics and Bayesian forecasting to deliver personalised, adaptive dosing recommendations. This approach captures inter-individual variability while linking serum drug concentrations to clinical response, enabling proactive dose adjustments using sparse or non-steady-state data. Emerging digital tools, point-of-care testing and integration of pharmacogenomics and biomarker profiling are expected to enhance MIPD's precision and accessibility. Once implemented in routine care, MIPD has the potential to transform biologic therapy dosing using a dynamic, patient-centric system that maximises clinical response, minimises overtreatment and supports sustainable healthcare delivery.
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