Cristin-resultat-ID: 1909566
Sist endret: 3. mars 2022, 15:45
NVI-rapporteringsår: 2021
Resultat
Vitenskapelig artikkel
2021

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

Bidragsytere:
  • Silje Watterdal Syversen
  • Guro Løvik Goll
  • Kristin Kaasen Jørgensen
  • Øystein Sandanger
  • Joseph Sexton
  • Inge Christoffer Olsen
  • mfl.

Tidsskrift

Journal of the American Medical Association (JAMA)
ISSN 0098-7484
e-ISSN 1538-3598
NVI-nivå 2

Om resultatet

Vitenskapelig artikkel
Publiseringsår: 2021
Publisert online: 2021
Trykket: 2021
Volum: 325
Hefte: 17
Sider: 1744 - 1754
Open Access

Importkilder

Scopus-ID: 2-s2.0-85105249877

Beskrivelse Beskrivelse

Tittel

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

Sammendrag

Importance: Proactive therapeutic drug monitoring (TDM), defined as individualized drug dosing based on scheduled monitoring of serum drug levels, has been proposed as an alternative to standard therapy to maximize efficacy and safety of infliximab and other biological drugs. However, whether proactive TDM improves clinical outcomes when implemented at the time of drug initiation, compared with standard therapy, remains unclear. Objective: To assess whether TDM during initiation of infliximab therapy improves treatment efficacy compared with standard infliximab therapy without TDM. Design, setting, and participants: Randomized, parallel-group, open-label clinical trial of 411 adults with rheumatoid arthritis, spondyloarthritis, psoriatic arthritis, ulcerative colitis, Crohn disease, or psoriasis initiating infliximab therapy in 21 hospitals in Norway. Patients were recruited from March 1, 2017, to January 10, 2019. Final follow-up occurred on November 5, 2019. Interventions: Patients were randomized 1:1 to receive proactive TDM with dose and interval adjustments based on scheduled monitoring of serum drug levels and antidrug antibodies (TDM group; n = 207) or standard infliximab therapy without drug and antibody level monitoring (standard therapy group; n = 204). Main outcomes and measures: The primary end point was clinical remission at week 30. Results: Among 411 randomized patients (mean age, 44.7 [SD, 14.9] years; 209 women [51%]), 398 (198 in the TDM group and 200 in the standard therapy group) received their randomized intervention and were included in the full analysis set. Clinical remission at week 30 was achieved in 100 (50.5%) of 198 and 106 (53.0%) of 200 patients in the TDM and standard therapy groups, respectively (adjusted difference, 1.5%; 95% CI, -8.2% to 11.1%; P = .78). Adverse events were reported in 135 patients (68%) and 139 patients (70%) in the TDM and standard therapy groups, respectively. Conclusions and relevance: Among patients with immune-mediated inflammatory diseases initiating treatment with infliximab, proactive therapeutic drug monitoring, compared with standard therapy, did not significantly improve clinical remission rates over 30 weeks. These findings do not support routine use of therapeutic drug monitoring during infliximab induction for improving disease remission rates.

Bidragsytere

Silje Watterdal Syversen

  • Tilknyttet:
    Forfatter
    ved Klinikk for revmatologi poliklinikk og forskning ved Diakonhjemmet sykehus

Guro Løvik Goll

  • Tilknyttet:
    Forfatter
    ved Klinikk for revmatologi poliklinikk og forskning ved Diakonhjemmet sykehus

Kristin Kaasen Jørgensen

  • Tilknyttet:
    Forfatter
    ved Avdeling for fordøyelsessykdommer ved Akershus universitetssykehus HF

Øystein Sandanger

  • Tilknyttet:
    Forfatter
    ved Seksjon for hudsykdommer ved Oslo universitetssykehus HF

Joseph Sexton

  • Tilknyttet:
    Forfatter
    ved Klinikk for revmatologi poliklinikk og forskning ved Diakonhjemmet sykehus
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