Evidence map›Paper›PMID 42057584›Full record

Observational studyClinical and translational science2026

Evaluation of a Therapeutic Drug Monitoring Strategy for Adalimumab in Psoriasis: A Prospective Pharmacokinetic-Pharmacodynamic Study.

Shan Pan, Teresa Tsakok, Ruoheng Wei, Nick Dand, Floris C Loeff, Karien Bloem, Annick de Vries, David Baudry, Michael Duckworth, Angela Pushpa-Rajah and 17 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Clinical and translational science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Shan PanSt John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Teresa TsakokSt John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-1895-6070
Ruoheng WeiSt John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0009-0004-7284-9676
Nick DandDepartment of Medical and Molecular Genetics, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.ORCID 0000-0002-1805-6278
Floris C LoeffSanquin Diagnostic Services, Amsterdam, the Netherlands.ORCID 0000-0001-7059-2038
Karien BloemSanquin Diagnostic Services, Amsterdam, the Netherlands.ORCID 0000-0003-4325-8223
Annick de VriesSanquin Diagnostic Services, Amsterdam, the Netherlands.ORCID 0000-0001-7570-473X
David BaudrySt John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.ORCID 0000-0003-0784-1286
Michael DuckworthSt John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.ORCID 0000-0003-0295-9621
Angela Pushpa-RajahSt John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.ORCID 0000-0002-7170-203X
Alice RussellSt John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Ali AlsharqiDermatology Department, Royal Liverpool and Broadgreen University Hospital Trust, Liverpool, UK.
Gabrielle BecherWest Glasgow Ambulatory Care Hospital, Glasgow, UK.ORCID 0000-0001-9836-2787
Ruth MurphyDepartment of Dermatology, Queens Medical Centre, Nottingham University Teaching Hospitals, Nottingham, UK.
Shyamal WahieDermatology Department, University Hospital of North Durham, Durham, UK.ORCID 0000-0003-2798-8429
Andrew WrightCentre for Skin Sciences, University of Bradford, Bradford, UK.ORCID 0000-0002-6072-5148
Christopher E M GriffithsCentre for Dermatology Research, University of Manchester, Manchester, UK.ORCID 0000-0001-5371-4427
Nick J ReynoldsInstitute of Translational and Clinical Medicine, Medical School, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-6484-825X
Jonathan BarkerSt John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-9030-183X
Richard B WarrenDermatology Centre, Northern Care Alliance NHS Foundation Trust, Manchester, UK.ORCID 0000-0002-2918-6481
A David BurdenInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.ORCID 0000-0001-7395-9931
Theo RispensDepartment of Immunopathology, Sanquin Research and Landsteiner Laboratory, Amsterdam, the Netherlands.ORCID 0000-0001-9600-1312
Satveer K MahilSt John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-4692-3794
Joseph F StandingSchool of Pharmacy, University College London, London, UK.ORCID 0000-0002-4561-7173
Catherine H SmithSt John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0001-9918-1144
BADBIR Study Group
BSTOP Study Group and the PSORT Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using a real-world psoriasis cohort, we established the pharmacokinetic-pharmacodynamic (PKPD) relationship for the biologic therapy adalimumab and evaluated the clinical utility and cost-effectiveness of a proactive therapeutic drug monitoring (TDM) strategy. A total of 543 patients on adalimumab monotherapy for psoriasis provided 946 pharmacokinetic samples and 1700 Psoriasis Area Severity Index (PASI) disease severity measurements. To describe the PASI change over time, a one-compartment linear PK model with first-order absorption and elimination was linked to a turnover mechanism of skin lesions. Based on the PKPD relationship and a predefined therapeutic range, real-time stochastic simulation was performed for a proactive TDM strategy, where trough levels guided dose escalation or reduction. Compared to the standard care, the TDM strategy improved PASI90 and PASI75 by 37.5% and 12.8%, respectively, with a 25.9% increase in drug costs. In the future, incorporating the PKPD model into a Bayesian therapeutic monitoring algorithm could facilitate individualized adalimumab dosing.

Indexed as

AdalimumabAntirheumatic AgentsDrug MonitoringPsoriasisAdolescentAdultAgedAged, 80 and overBayes TheoremComputer SimulationCost-Effectiveness AnalysisDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedAdalimumabAntirheumatic Agentsadalimumabpharmacokinetic‐pharmacodynamicpsoriasisreal‐worldtherapeutic drug monitoring

Identifiers

PMID42057584
PMCPMC13129494

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.