Silje Watterdal Syversen1, Kristin Kaasen Jørgensen2, Guro Løvik Goll1, Marthe Kirkesæther Brun1,3, Øystein Sandanger4, Kristin Hammersbøen Bjørlykke2,3, Joseph Sexton1, Inge Christoffer Olsen5, Johanna Elin Gehin3,6, David John Warren6, Rolf Anton Klaasen6, Geir Noraberg7, Trude Jannecke Bruun8, Christian Kvikne Dotterud9, Maud Kristine Aga Ljoså10, Anne Julsrud Haugen11, Rune Johan Njålla12, Camilla Zettel13, Carl Magnus Ystrøm14, Yngvill Hovde Bragnes15, Svanaug Skorpe16, Turid Thune17, Kathrine Aglen Seeberg18, Brigitte Michelsen19, Ingrid Marianne Blomgren20, Eldri Kveine Strand21, Pawel Mielnik22, Roald Torp23, Cato Mørk24, Tore K Kvien1,3, Jørgen Jahnsen2,3, Nils Bolstad6, Espen A Haavardsholm1,3. 1. Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway. 2. Department of Gastroenterology, Akershus University Hospital, Lørenskog, Norway. 3. Faculty of Medicine, University of Oslo, Oslo, Norway. 4. Section of Dermatology, Oslo University Hospital, Oslo, Norway. 5. Department of Research Support for Clinical Trials, Oslo University Hospital, Oslo, Norway. 6. Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway. 7. Department of Gastroenterology, Hospital of Southern Norway Trust, Arendal, Norway. 8. Department of Rheumatology, The University Hospital of North Norway, Tromsø, Norway. 9. Department of Dermatology, St Olavs Hospital, Trondheim University Hospital, Trondheim, Norway. 10. Department of Rheumatology, Ålesund Hospital, Ålesund, Norway. 11. Department of Rheumatology, Østfold Hospital Trust, Moss, Norway. 12. Department of Rheumatology, Nordland Hospital Trust, Bodø, Norway. 13. Department of Rheumatology, Betanien Hospital, Skien, Norway. 14. Department of Medicine, Innlandet Hospital Trust, Elverum, Norway. 15. Department of Rheumatology, Vestre Viken Hospital Trust, Drammen, Norway. 16. Haugesund Hospital for Rheumatic Diseases, Haugesund, Norway. 17. Department of Dermatology, Haukeland University Hospital, Bergen, Norway. 18. Department of Gastroenterology, Vestfold Hospital Trust, Tønsberg, Norway. 19. Division of Rheumatology, Department of Medicine, Hospital of Southern Norway Trust, Kristiansand, Norway. 20. Department of Gastroenterology, Fonna Hospital Trust, Haugesund, Norway. 21. Lillehammer Hospital for Rheumatic Diseases, Lillehammer, Norway. 22. Department of Neurology, Rheumatology, and Physical Medicine, Førde Hospital Trust, Førde, Norway. 23. Department of Medicine, Innlandet Hospital Trust, Hamar, Norway. 24. Akershus Dermatology Center, Lørenskog, Norway.
Abstract
Importance: 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. Objective: To assess whether proactive TDM during maintenance therapy with infliximab improves treatment efficacy by preventing disease worsening compared with standard infliximab therapy without TDM. Design, Setting, and Participants: 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. Interventions: 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). Main Outcome and Measures: 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. Results: 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. Conclusions and Relevance: 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. Trial Registration: ClinicalTrials.gov Identifier: NCT03074656.
Importance: 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. Objective: To assess whether proactive TDM during maintenance therapy with infliximab improves treatment efficacy by preventing disease worsening compared with standard infliximab therapy without TDM. Design, Setting, and Participants: 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. Interventions: 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). Main Outcome and Measures: 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. Results: 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. Conclusions and Relevance: 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. Trial Registration: ClinicalTrials.gov Identifier: NCT03074656.
Authors: Geert D'Haens; William J Sandborn; Brian G Feagan; Karel Geboes; Stephen B Hanauer; E Jan Irvine; Marc Lémann; Philippe Marteau; Paul Rutgeerts; Jurgen Schölmerich; Lloyd R Sutherland Journal: Gastroenterology Date: 2006-12-20 Impact factor: 22.682
Authors: Dan Turner; Amanda Ricciuto; Ayanna Lewis; Ferdinando D'Amico; Jasbir Dhaliwal; Anne M Griffiths; Dominik Bettenworth; William J Sandborn; Bruce E Sands; Walter Reinisch; Jürgen Schölmerich; Willem Bemelman; Silvio Danese; Jean Yves Mary; David Rubin; Jean-Frederic Colombel; Laurent Peyrin-Biroulet; Iris Dotan; Maria T Abreu; Axel Dignass Journal: Gastroenterology Date: 2021-02-19 Impact factor: 22.682
Authors: Konstantinos Papamichael; Adam S Cheifetz; Gil Y Melmed; Peter M Irving; Niels Vande Casteele; Patricia L Kozuch; Laura E Raffals; Leonard Baidoo; Brian Bressler; Shane M Devlin; Jennifer Jones; Gilaad G Kaplan; Miles P Sparrow; Fernando S Velayos; Thomas Ullman; Corey A Siegel Journal: Clin Gastroenterol Hepatol Date: 2019-03-27 Impact factor: 11.382
Authors: Christopher Andrew Lamb; Nicholas A Kennedy; Tim Raine; Philip Anthony Hendy; Philip J Smith; Jimmy K Limdi; Bu'Hussain Hayee; Miranda C E Lomer; Gareth C Parkes; Christian Selinger; Kevin J Barrett; R Justin Davies; Cathy Bennett; Stuart Gittens; Malcolm G Dunlop; Omar Faiz; Aileen Fraser; Vikki Garrick; Paul D Johnston; Miles Parkes; Jeremy Sanderson; Helen Terry; Daniel R Gaya; Tariq H Iqbal; Stuart A Taylor; Melissa Smith; Matthew Brookes; Richard Hansen; A Barney Hawthorne Journal: Gut Date: 2019-09-27 Impact factor: 23.059
Authors: Konstantinos Papamichael; Karen A Chachu; Ravy K Vajravelu; Byron P Vaughn; Josephine Ni; Mark T Osterman; Adam S Cheifetz Journal: Clin Gastroenterol Hepatol Date: 2017-03-30 Impact factor: 11.382
Authors: J Berth-Jones; K Grotzinger; C Rainville; B Pham; J Huang; S Daly; M Herdman; P Firth; K Hotchkiss Journal: Br J Dermatol Date: 2006-10 Impact factor: 9.302
Authors: Konstantinos Papamichael; Thomas Van Stappen; Niels Vande Casteele; Ann Gils; Thomas Billiet; Sophie Tops; Karolien Claes; Gert Van Assche; Paul Rutgeerts; Severine Vermeire; Marc Ferrante Journal: Clin Gastroenterol Hepatol Date: 2015-12-08 Impact factor: 11.382
Authors: Pedro Machado; Robert Landewé; Elisabeth Lie; Tore K Kvien; Jürgen Braun; Daniel Baker; Désirée van der Heijde Journal: Ann Rheum Dis Date: 2010-11-10 Impact factor: 19.103
Authors: Charlotte Krieckaert; Borja Hernández-Breijo; Johanna Elin Gehin; Guillaume le Mélédo; Alejandro Balsa; Meghna Jani; Denis Mulleman; Victoria Navarro-Compan; Gertjan Wolbink; John Isaac; Astrid van Tubergen Journal: RMD Open Date: 2022-06
Authors: Gerasimos Evangelatos; Giorgos Bamias; George D Kitas; George Kollias; Petros P Sfikakis Journal: Rheumatol Int Date: 2022-05-03 Impact factor: 3.580
Authors: Wannee Kantasiripitak; An Outtier; Sebastian G Wicha; Alexander Kensert; Zhigang Wang; João Sabino; Séverine Vermeire; Debby Thomas; Marc Ferrante; Erwin Dreesen Journal: CPT Pharmacometrics Syst Pharmacol Date: 2022-06-15