Association of Serum Ustekinumab Levels With Clinical Response in Psoriasis.


Journal

JAMA dermatology
ISSN: 2168-6084
Titre abrégé: JAMA Dermatol
Pays: United States
ID NLM: 101589530

Informations de publication

Date de publication:
01 Nov 2019
Historique:
pubmed: 19 9 2019
medline: 19 9 2019
entrez: 19 9 2019
Statut: ppublish

Résumé

High-cost biologic therapies have transformed the management of immune-mediated inflammatory diseases. To optimize outcomes and reduce costs, dose adjustment informed by measurement of circulating drug levels has been shown to be effective in various settings. However, limited evidence exists for this approach with the interleukin 12 and interleukin 23 inhibitor ustekinumab. To evaluate clinical utility of therapeutic drug monitoring for ustekinumab in patients with psoriasis. A prospective observational cohort of 491 adults with psoriasis was recruited to the multicenter Biomarkers of Systemic Treatment Outcomes in Psoriasis study within the British Association of Dermatologists Biologic and Immunomodulators Register from June 2009 to December 2017; samples from some patients were taken between 2009 and 2011 as part of a pilot study with the same inclusion criteria. Serum ustekinumab level measured at any point during the dosing cycle using an enzyme-linked immunosorbent assay. Disease activity measured using the Psoriasis Area and Severity Index (PASI) score. Treatment response outcomes were PASI75 (75% reduction in PASI score from baseline [primary outcome]), PASI90 (90% reduction of PASI score from baseline), and absolute PASI score of 1.5 or less. A total of 491 patients (171 women and 320 men; mean [SD] age, 45.7 [12.8] years) had 1 or more serum samples (total, 853 samples obtained 0-56 weeks from start of treatment) and 1 or more PASI scores within the first year of treatment. Antidrug antibodies were detected in only 17 of 490 patients (3.5%). Early measured drug levels (1-12 weeks after starting treatment) were associated with PASI75 response 6 months after starting treatment (odds ratio, 1.38; 95% CI, 1.11-1.71) when adjusted for baseline PASI score, age, and ustekinumab dose. However, this finding was not consistent across the other PASI outcomes (PASI90 and PASI score of ≤1.5). This real-world study provides evidence that measurement of early serum ustekinumab levels could be useful to direct the treatment strategy for psoriasis. Adequate drug exposure early in the treatment cycle may be particularly important in determining clinical outcome.

Identifiants

pubmed: 31532460
pii: 2751372
doi: 10.1001/jamadermatol.2019.1783
pmc: PMC6751771
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1235-1243

Subventions

Organisme : Medical Research Council
ID : MR/S003126/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_14119
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_15059
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M008665/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R001839/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L011808/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N005872/1
Pays : United Kingdom

Auteurs

Teresa Tsakok (T)

St John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.
St John's Institute of Dermatology, Guy's and St Thomas' National Health Service Foundation Trust, London, United Kingdom.

Nina Wilson (N)

Institute of Health and Society, Faculty of Medical Sciences, Newcastle University, Newcastle-upon-Tyne, United Kingdom.

Nick Dand (N)

Department of Medical and Molecular Genetics, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.

Floris C Loeff (FC)

Department of Immunopathology, Sanquin Research and Landsteiner Laboratory, Amsterdam, the Netherlands.

Karien Bloem (K)

Biologics Lab, Sanquin Diagnostic Services, Amsterdam, the Netherlands.

David Baudry (D)

St John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.

Michael Duckworth (M)

St John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.

Shan Pan (S)

Infection, Immunity, Inflammation Section, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.

Angela Pushpa-Rajah (A)

St John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.

Joseph F Standing (JF)

Infection, Immunity, Inflammation Section, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.

Annick de Vries (A)

Biologics Lab, Sanquin Diagnostic Services, Amsterdam, the Netherlands.

Ali Alsharqi (A)

Department of Dermatology, Royal Liverpool and Broadgreen University Hospital Trust, Liverpool, United Kingdom.

Gabrielle Becher (G)

West Glasgow Ambulatory Care Hospital, Glasgow, United Kingdom.

Ruth Murphy (R)

Department of Dermatology, Queens Medical Centre, Nottingham University Teaching Hospitals, Nottingham, United Kingdom.

Shyamal Wahie (S)

Department of Dermatology, University Hospital of North Durham, Durham, United Kingdom.

Andrew Wright (A)

Centre for Skin Sciences, University of Bradford, Bradford, United Kingdom.

Christopher E M Griffiths (CEM)

Dermatology Centre, Salford Royal National Health Service Foundation Trust, Manchester, United Kingdom.
The University of Manchester, Manchester Academic Health Science Centre, National Institute for Health Research Manchester Biomedical Research Centre, Manchester, United Kingdom.

Nick J Reynolds (NJ)

Dermatology Sciences, Institute of Cellular Medicine, Medical School, Newcastle University, Newcastle upon Tyne, United Kingdom.
Department of Dermatology, Royal Victoria Infirmary, Newcastle Hospitals National Health Service Foundation Trust, Newcastle upon Tyne, United Kingdom.

Jonathan Barker (J)

St John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.
St John's Institute of Dermatology, Guy's and St Thomas' National Health Service Foundation Trust, London, United Kingdom.

Richard B Warren (RB)

Dermatology Centre, Salford Royal National Health Service Foundation Trust, Manchester, United Kingdom.

A David Burden (AD)

Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.

Theo Rispens (T)

Department of Immunopathology, Sanquin Research and Landsteiner Laboratory, Amsterdam, the Netherlands.

Deborah Stocken (D)

Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, United Kingdom.

Catherine Smith (C)

St John's Institute of Dermatology, School of Basic & Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.
St John's Institute of Dermatology, Guy's and St Thomas' National Health Service Foundation Trust, London, United Kingdom.

Classifications MeSH