Clinical Trial: A Pragmatic Randomised Controlled Study to Assess the Effectiveness of Two Patient Management Strategies in Mild to Moderate Ulcerative Colitis—The OPTIMISE Study

Author:

Danese Silvio1ORCID,Fiorino Gionata2ORCID,Vicaut Eric3ORCID,Paridaens Kristine4ORCID,Ugur Asiya5ORCID,Clark Brian5,Vanasek Tomas6,Stepek David7,D’Amico Ferdinando1ORCID,West Rachel8,Gilissen Lennard P. L.9,Wisniewska Jarosinka Maria10,Drobinski Piotr11,Fronik Grzegorz12,Fic Mirosław13,Walczak Michał14,Kowalski Maciej15,Korczowski Bartosz16ORCID,Wiatr Michal17,Peyrin-Biroulet Laurent181920212223

Affiliation:

1. Department of Gastroenterology and Digestive Endoscopy, San Raffaele Hospital, Vita-Salute San Raffaele University, 20132 Milan, Italy

2. IBD Unit, Department of Gastroenterology and Digestive Endoscopy, San Camillo-Forlanini Hospital, 00152 Rome, Italy

3. Clinical Trial Unit, Hospital Lariboisière APHP, 75010 Paris, France

4. Ferring International Center S.A, 1162 Saint-Prex, Switzerland

5. Ferring Pharmaceuticals A/S, 2770 Kastrup, Denmark

6. Hepato-Gastroenterologie HK, s.r.o., 50012 Hradec Králové, Czech Republic

7. Internal Department, Military Hospital Brno, 61500 Brno, Czech Republic

8. Department of Gastroenterology and Hepatology, Franciscus Gasthuis & Vlietland, 3045 PM Rotterdam, The Netherlands

9. Department of Gastroenterology and Hepatology, Catharina Hospital Eindhoven, 5623 EJ Eindhoven, The Netherlands

10. Department of Gastroenterology, Medical University of Lodz, 92-213 Lodz, Poland

11. Centrum Medyczne Lukamed in Chojnice, 89-600 Chojnice, Poland

12. Melita Medical—Centrum Proktologii, Onkologii i Chorób Jelit, 50-449 Wrocław, Poland

13. Polish Society of Gastroenterology, 58-521 Jezów Sudecki, Poland

14. Institute of Human Genetics, Polish Academy of Sciences, 61-772 Poznan, Poland

15. Department of Gastroenterology, Centrum Diagnostyczno—Lecznicze Barska, 87-806 Włocławek, Poland

16. Institute of Medical Sciences, Medical College, University of Rzeszów, 35-310 Rzeszów, Poland

17. Ośrodek Badań Klinicznych CLINSANTE S.C. Ewa Galczak-Nowak Małgorzata Trzaska, Chałubińskiego, 85-004 Bydgoszcz, Poland

18. Department of Gastroenterology and Inserm NGERE U1256, University Hospital of Nancy, University of Lorraine, 54000 Vandoeuvre-lès-Nancy, France

19. Department of Gastroenterology, Nancy University Hospital, 54500 Vandœuvre-lès-Nancy, France

20. INFINY Institute, Nancy University Hospital, 54500 Vandœuvre-lès-Nancy, France

21. FHU-CURE, Nancy University Hospital, 54500 Vandœuvre-lès-Nancy, France

22. Groupe Hospitalier Privé Ambroise Paré—Hartmann, Paris IBD Center, 92200 Neuilly sur Seine, France

23. Division of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, QC H4A 3J1, Canada

Abstract

Background: Current management of mild-to-moderate ulcerative colitis (UC) involves monitoring clinical markers of disease activity, such as stool frequency (SF) and rectal bleeding (RB), and adjusting treatment accordingly. Our aim was to assess whether targeting treatment based on faecal calprotectin (FC) levels (treat-to-target; T2T) provides greater UC disease control versus a symptom-based approach. Methods: This was a pragmatic, randomised (1:1) controlled study of patients with mild-to-moderate UC (global Mayo score 2–6) treated with ≤2.4 g/day 5-aminosalicylic acid that compared the effectiveness of two management strategies with (interventional arm) and without (reference arm) FC home monitoring over 12 months of follow-up. Treatment was optimised in the interventional arm using FC values and clinical symptoms (PRO-2), while the reference arm used only PRO-2. Results: 193 patients completed the study. No significant difference was found for the primary endpoint (Mayo Endoscopic Subscore [MES] = 0 at 12 months). A numerical advantage for the interventional arm over the reference arm for the primary endpoint (37.0% vs. 33.4%, respectively) and for MES ≤ 1, RB = 0, and SF ≤ 1 at 12 months was found following imputation for missing data. The composite endpoint of MES = 0, RB = 0, and SF ≤ 1 at 12 months was achieved at a significantly higher rate in the interventional arm than the reference arm (effect size [ES]: 0.17, 95% CI 0.02–0.32; p < 0.05). A similar result was obtained for MES ≤ 1, RB = 0 and SF ≤ 1 (ES: 0.22; 95% CI 0.07–0.37; p < 0.05). Conclusions: T2T using FC monitoring was effective in patients with mild-to-moderate UC at 12 months. Further longer-term studies are required to confirm the results.

Funder

Ferring Pharmaceuticals

Publisher

MDPI AG

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