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A pan-European register-based observational study of abrocitinib and conventional systemic therapies in moderate and
Elizaveta Gribaleva1, Niels Steen Krogh2, David Prieto-Merino1,3
1Unit for Paediatric and Population-Based Dermatology Research, St John's Institute of Dermatology, King's College London, London, UK.
Background:
Atopic dermatitis (AD) is a common chronic inflammatory skin condition. Currently, there is a lack of real-world evidence regarding the effectiveness of systemic therapies for moderate-to-severe AD. Abrocitinib is a novel Janus kinase 1 selective inhibitor licensed for AD in adults and adolescents requiring systemic treatment. The DREAM TO TREAT AD (D2T AD) study was set up to collect real-world data on abrocitinib and conventional systemic treatment use in moderate-to-severe AD. It aims to describe treatment patterns and effectiveness within a 3-year follow-up period in five registers: Ireland [Atopic Eczema Systemic Therapy Register (A-STAR) Ireland], Denmark (SCRATCH), Germany (TREATgermany), the Netherlands and Belgium (TREAT NL/BE), and the UK (A-STAR UK).
Methods:
The study protocol and methodology were developed collaboratively by academics of the participating registers with the study funder. The study follow-up timepoints and outcomes are based on an international Delphi exercise previously run by the TREAT Registry Taskforce. All five registers collect data in several domains, including patients' characteristics and treatment outcomes in patients receiving systemic treatment. Assignment to treatment was decided by the treating clinician. Data collected by the registers will be transformed into harmonized datasets and then to analytical datasets (ADS) to address research questions. Study objectives include describing patient baseline characteristics, in addition to clinician- (Eczema Area and Severity Index) and patient-reported outcomes [Patient-Reported Eczema Measure (POEM), Children's/Dermatology Life Quality Index (C/DLQI), Peak Pruritus Numeric Rate Scale (PP-NRS)] at baseline and follow-up, as well as treatment patterns while on abrocitinib and conventional systemic treatments. The ADS will be analysed using the novel DataSHIELD solution that enables centralized statistical analysis on decentralized data (i.e. without data leaving the register of origin). The DataSHIELD solution includes central analytic hubs (CAHs) and local data nodes (LDNs). CAH can remotely interrogate LDNs via an internet connection using analytical commands. Each LDN produces local statistical results that are sent back to the CAH, which can then combine the results from all LNDs without seeing any patient-level data.
Discussion:
D2T AD undertakes a novel federated data analysis approach across five registers in observational dermatology research and will provide crucial information on AD treatment outcomes for clinical decision-making, in addition to proving the feasibility of this type of scientific collaboration.
Protocol Registration:
EMA RWD Catalogue (EU PAS no.: 108468; study ID: 199009; https://catalogues.ema.europa.eu/node/3894/administrative-details).
Insights
The DREAM TO TREAT AD (D2T AD) study collects real-world data on abrocitinib and conventional systemic therapies for moderate-to-severe atopic dermatitis (AD). It assesses treatment patterns and effectiveness across five international registers using a novel federated analysis approach.
Area of Science:
- Dermatology
- Real-world evidence
- Pharmacovigilance
Background:
- Atopic dermatitis (AD) is a prevalent chronic inflammatory skin condition.
- There is a need for real-world data on systemic therapies for moderate-to-severe AD.
- Abrocitinib, a JAK1 inhibitor, is a treatment option for AD.
Purpose of the Study:
- To collect real-world data on abrocitinib and conventional systemic treatments for moderate-to-severe AD.
- To describe treatment patterns and effectiveness over a 3-year follow-up period.
- To evaluate outcomes across five international patient registers.
Main Methods:
- The DREAM TO TREAT AD (D2T AD) study utilizes data from five national registers.
- A federated data analysis approach (DataSHIELD) enables centralized analysis of decentralized data.
- Clinician- and patient-reported outcomes are collected at baseline and follow-up.
Main Results:
- Data collection is ongoing across Ireland, Denmark, Germany, the Netherlands, Belgium, and the UK.
- The study will provide insights into patient characteristics and treatment outcomes.
- Federated analysis ensures data privacy while enabling robust statistical analysis.
Conclusions:
- The D2T AD study employs a novel federated analysis approach for observational dermatology research.
- It will generate crucial real-world evidence for clinical decision-making in AD management.
- The study demonstrates the feasibility of international scientific collaboration using decentralized data.
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