Effect of Therapeutic Drug Monitoring vs Standard Therapy During Maintenance Infliximab Therapy on Disease Control in Patients With Immune-Mediated Inflammatory Diseases: A Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
21 12 2021
Historique:
entrez: 21 12 2021
pubmed: 22 12 2021
medline: 13 1 2022
Statut: ppublish

Résumé

Proactive therapeutic drug monitoring (TDM), consisting of individualized treatment based on scheduled assessments of serum drug levels, has been proposed as an alternative to standard therapy to optimize efficacy and safety of infliximab and other biologic drugs. However, it remains unclear whether proactive TDM improves clinical outcomes during maintenance therapy. To assess whether proactive TDM during maintenance therapy with infliximab improves treatment efficacy by preventing disease worsening compared with standard infliximab therapy without TDM. Randomized, parallel-group, open-label clinical trial including 458 adults with rheumatoid arthritis, spondyloarthritis, psoriatic arthritis, ulcerative colitis, Crohn disease, or psoriasis undergoing maintenance therapy with infliximab in 20 Norwegian hospitals. Patients were recruited from June 7, 2017, to December 12, 2019. Final follow-up took place on December 14, 2020. Patients were randomized 1:1 to proactive TDM with dose and interval adjustments based on scheduled monitoring of serum drug levels and antidrug antibodies (TDM group; n = 228) or to standard infliximab therapy without drug and antibody level monitoring (standard therapy group; n = 230). The primary outcome was sustained disease control without disease worsening, defined by disease-specific composite scores or consensus about disease worsening between patient and physician leading to a major change in treatment (switching to another biologic drug, adding an immunosuppressive drug including glucocorticoids, or increasing the infliximab dose), during the 52-week study period. Among 458 randomized patients (mean age, 44.8 [SD, 14.3] years; 216 women [49.8%]), 454 received their randomly allocated intervention and were included in the full analysis set. The primary outcome of sustained disease control without disease worsening was observed in 167 patients (73.6%) in the TDM group and 127 patients (55.9%) in the standard therapy group. The estimated adjusted difference was 17.6% (95% CI, 9.0%-26.2%; P < .001) favoring TDM. Adverse events were reported in 137 patients (60%) and 142 patients (63%) in the TDM and standard therapy groups, respectively. Among patients with immune-mediated inflammatory diseases undergoing maintenance therapy with infliximab, proactive TDM was more effective than treatment without TDM in sustaining disease control without disease worsening. Further research is needed to compare proactive TDM with reactive TDM, to assess the effects on long-term disease complications, and to evaluate the cost-effectiveness of this approach. ClinicalTrials.gov Identifier: NCT03074656.

Identifiants

pubmed: 34932077
pii: 2787318
doi: 10.1001/jama.2021.21316
pmc: PMC8693274
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0
Infliximab B72HH48FLU

Banques de données

ClinicalTrials.gov
['NCT03074656']

Types de publication

Clinical Trial, Phase IV Comparative Study Equivalence Trial Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2375-2384

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

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Auteurs

Silje Watterdal Syversen (SW)

Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

Kristin Kaasen Jørgensen (KK)

Department of Gastroenterology, Akershus University Hospital, Lørenskog, Norway.

Guro Løvik Goll (GL)

Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

Marthe Kirkesæther Brun (MK)

Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway.

Øystein Sandanger (Ø)

Section of Dermatology, Oslo University Hospital, Oslo, Norway.

Kristin Hammersbøen Bjørlykke (KH)

Department of Gastroenterology, Akershus University Hospital, Lørenskog, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway.

Joseph Sexton (J)

Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

Inge Christoffer Olsen (IC)

Department of Research Support for Clinical Trials, Oslo University Hospital, Oslo, Norway.

Johanna Elin Gehin (JE)

Faculty of Medicine, University of Oslo, Oslo, Norway.
Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.

David John Warren (DJ)

Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.

Rolf Anton Klaasen (RA)

Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.

Geir Noraberg (G)

Department of Gastroenterology, Hospital of Southern Norway Trust, Arendal, Norway.

Trude Jannecke Bruun (TJ)

Department of Rheumatology, The University Hospital of North Norway, Tromsø, Norway.

Christian Kvikne Dotterud (CK)

Department of Dermatology, St Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.

Maud Kristine Aga Ljoså (MKA)

Department of Rheumatology, Ålesund Hospital, Ålesund, Norway.

Anne Julsrud Haugen (AJ)

Department of Rheumatology, Østfold Hospital Trust, Moss, Norway.

Rune Johan Njålla (RJ)

Department of Rheumatology, Nordland Hospital Trust, Bodø, Norway.

Camilla Zettel (C)

Department of Rheumatology, Betanien Hospital, Skien, Norway.

Carl Magnus Ystrøm (CM)

Department of Medicine, Innlandet Hospital Trust, Elverum, Norway.

Yngvill Hovde Bragnes (YH)

Department of Rheumatology, Vestre Viken Hospital Trust, Drammen, Norway.

Svanaug Skorpe (S)

Haugesund Hospital for Rheumatic Diseases, Haugesund, Norway.

Turid Thune (T)

Department of Dermatology, Haukeland University Hospital, Bergen, Norway.

Kathrine Aglen Seeberg (KA)

Department of Gastroenterology, Vestfold Hospital Trust, Tønsberg, Norway.

Brigitte Michelsen (B)

Division of Rheumatology, Department of Medicine, Hospital of Southern Norway Trust, Kristiansand, Norway.

Ingrid Marianne Blomgren (IM)

Department of Gastroenterology, Fonna Hospital Trust, Haugesund, Norway.

Eldri Kveine Strand (EK)

Lillehammer Hospital for Rheumatic Diseases, Lillehammer, Norway.

Pawel Mielnik (P)

Department of Neurology, Rheumatology, and Physical Medicine, Førde Hospital Trust, Førde, Norway.

Roald Torp (R)

Department of Medicine, Innlandet Hospital Trust, Hamar, Norway.

Cato Mørk (C)

Akershus Dermatology Center, Lørenskog, Norway.

Tore K Kvien (TK)

Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway.

Jørgen Jahnsen (J)

Department of Gastroenterology, Akershus University Hospital, Lørenskog, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway.

Nils Bolstad (N)

Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.

Espen A Haavardsholm (EA)

Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway.

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