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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.
Syversen, Silje Watterdal; Goll, Guro Løvik; Jørgensen, Kristin Kaasen; Sandanger, Øystein; Sexton, Joseph; Olsen, Inge Christoffer; Gehin, Johanna Elin; Warren, David John; Brun, Marthe Kirkesæther; Klaasen, Rolf Anton; Karlsen, Lars Normann; Noraberg, Geir; Zettel, Camilla; Ljoså, Maud Kristine Aga; Haugen, Anne Julsrud; Njålla, Rune Johan; Bruun, Trude Jannecke; Seeberg, Kathrine Aglen; Michelsen, Brigitte; Strand, Eldri Kveine; Skorpe, Svanaug; Blomgren, Ingrid Marianne; Bragnes, Yngvill Hovde; Dotterud, Christian Kvikne; Thune, Turid; Ystrøm, Carl Magnus; Torp, Roald; Mielnik, Pawel; Mørk, Cato; Kvien, Tore K; Jahnsen, Jørgen; Bolstad, Nils; Haavardsholm, Espen A.
Afiliação
  • Syversen SW; Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
  • Goll GL; Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
  • Jørgensen KK; Department of Gastroenterology, Akershus University Hospital, Lørenskog, Norway.
  • Sandanger Ø; Section of Dermatology, Oslo University Hospital, Oslo, Norway.
  • Sexton J; Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
  • Olsen IC; Department of Research Support for Clinical Trials, Oslo University Hospital, Oslo, Norway.
  • Gehin JE; Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
  • Warren DJ; Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Brun MK; Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
  • Klaasen RA; Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
  • Karlsen LN; Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Noraberg G; Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
  • Zettel C; Department of Gastroenterology, Stavanger University Hospital, Stavanger, Norway.
  • Ljoså MKA; Department of Gastroenterology, Hospital of Southern Norway Trust, Arendal, Norway.
  • Haugen AJ; Department of Rheumatology, Betanien Hospital, Skien, Norway.
  • Njålla RJ; Department of Rheumatology, Ålesund Hospital, Ålesund, Norway.
  • Bruun TJ; Department of Rheumatology, Østfold Hospital Trust, Moss, Norway.
  • Seeberg KA; Department of Rheumatology, Nordland Hospital Trust, Bodø, Norway.
  • Michelsen B; Department of Rheumatology, University Hospital of North Norway, Tromsø, Norway.
  • Strand EK; Departement of Gastroenterology, Vestfold Hospital Trust, Tønsberg, Norway.
  • Skorpe S; Division of Rheumatology, Department of Medicine, Hospital of Southern Norway Trust, Kristiansand, Norway.
  • Blomgren IM; Lillehammer Hospital for Rheumatic Diseases, Lillehammer, Norway.
  • Bragnes YH; Haugesund Hospital for Rheumatic Diseases, Haugesund, Norway.
  • Dotterud CK; Department of Gastroenterology, Fonna Hospital Trust, Haugesund, Norway.
  • Thune T; Department of Rheumatology, Vestre Viken Hospital Trust, Drammen, Norway.
  • Ystrøm CM; Department of Dermatology, St Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
  • Torp R; Department of Dermatology, Haukeland University Hospital, Bergen, Norway.
  • Mielnik P; Department of Medicine, Innlandet Hospital Trust, Elverum, Norway.
  • Mørk C; Department of Medicine, Innlandet Hospital Trust, Hamar, Norway.
  • Kvien TK; Department of Neurology, Rheumatology, and Physical Medicine, Førde Hospital Trust, Førde, Norway.
  • Jahnsen J; Akershus Dermatology Center, Lørenskog, Norway.
  • Bolstad N; Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
  • Haavardsholm EA; Faculty of Medicine, University of Oslo, Oslo, Norway.
JAMA ; 325(17): 1744-1754, 2021 05 04.
Article em En | MEDLINE | ID: mdl-33944876
ABSTRACT
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 11 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. Trial Registration ClinicalTrials.gov Identifier NCT03074656.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite / Doenças Inflamatórias Intestinais / Monitoramento de Medicamentos / Infliximab Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite / Doenças Inflamatórias Intestinais / Monitoramento de Medicamentos / Infliximab Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article