Discontinuation of Infliximab Therapy in Patients With Crohn's Disease During Sustained Complete Remission (STOP IT)

Discontinuation of Infliximab Therapy in Patients With Crohn's Disease During Sustained Complete Remission: A Multi-center, Double Blinded, Randomized, Placebo Controlled Study

The purpose of this study is to determine whether infliximab can favourably and safely be discontinued in patients with Crohn's disease in sustained complete clinical, biochemical, and endoscopic remission on infliximab.

Further to examine the clinical utility of measuring levels/activity of infliximab and activity of anti-infliximab Ab in patients in sustained complete remission, in order to investigate whether pharmacoimmunological data can predict the clinical outcome and rationalize therapeutic management of these patients with respect to continuation or discontinuation of infliximab therapy. Additional, to investigate the optimal time-point, out of three, to measure this activity.

Study Overview

• Status: Completed
• Conditions: Crohn Disease
• Intervention / Treatment: Other: Placebo; Drug: Infliximab

Detailed Description

Recent guidelines for the management of Crohn's disease conclude that currently available data are insufficient to make firm recommendations on when and in whom to stop TNF-α antibody (TNF-α Ab) treatment after having obtained clinical remission. Further, the term "remission" is not well uniformly defined and may incorporate one or more features such as clinical remission, as assessed by CDAI, biochemical remission, endoscopical remission etc. The recently published prospective STORI study of 115 patients with luminal Crohn's disease reported that 56% of patients with Crohn's disease who had discontinued infliximab (IFX) while in clinical remission, maintained remission one year after discontinuation of therapy. Predictors of relapse included certain clinical features as well as objective biochemical and endoscopical markers of disease activity. Consistent with these data, we have recently reported that 61% of our own patients with Crohn's disease, who discontinued IFX while in complete clinical, steroid free IFX induced remission, maintained remission after one year; and half the patients were still in remission after nearly two years (median 680 days [412-948]).

A prospective randomized study of patients with Crohn's disease is necessary to confirm and extend the limited findings above, and assess whether IFX can be safely discontinued in a selected subgroup of patients with complete clinical, biochemical, and endoscopical remission.

Methods:

Study design: Prospective, double-blinded, randomized, placebo-controlled, Danish multi-center study with estimated seven Danish participating centers. Patients and treating physicians are blinded for the type of intervention.

Study population: Patients with luminal Crohn's disease in sustained complete remission on IFX.

Study treatment: Patients are randomized to either continue IFX treatment at an unchanged dosage and frequency, or alternatively to receive matching placebo. All patients will be graded for disease activity (Crohn's Disease Activity Index (CDAI), biochemical parameters, endoscopy, and/or MRI). Following screening and inclusion patients are seen after four weeks, and then every eight weeks. Endpoints are assessed at 48 weeks.

Investigators will, as explorative analyses, examine the clinical utility of measuring IFX levels and antibodies against IFX in patients with complete remission, in order to investigate whether pharmacoimmunological data can predict the clinical outcome and rationalize therapeutic management of these patients with respect to continuation or discontinuation of IFX therapy. Additional, investigators will investigate the optimal time-point out of three to measure this activity. Patients will on the day of infusion have three blood samples drawn: one just before infusion (trough), one right after the infusion (obtained from the other arm)(peak) and one an hour after infusion (C1). Samples will be measured by common solid - and fluid phase assays for this purpose, e.g. Reporter Gene Assay (RGA).

• Study Type: Interventional
• Enrollment (Actual): 115
• Phase: Phase 4

Contacts and Locations

Study Locations

• Denmark
  • Herlev, Denmark, 2730
    • Herlev Hospital, department of gastroenterology medical section
  • Herning, Denmark
    • Hospital enheden vest Herning
  • Hvidovre, Denmark
    • Hvidovre Hospital
  • Silkeborg, Denmark
    • Silkeborg Regional Hospital, Diagnostic Center
  • Slagelse, Denmark, 4200
    • Slagelse Sygehus
  • Aarhus C
    • Aarhus, Aarhus C, Denmark, 8000
      • Aarhus University Hospital
  • Copenhagen NV
    • Copenhagen, Copenhagen NV, Denmark, 2400
      • Bispebjerg Hospital
  • Nykøbing
    • Nykøbing Falster, Nykøbing, Denmark, 4800
      • Nykøbing F. Sygehus
  • Odense C
    • Odense, Odense C, Denmark, 5000
      • Odense University Hospital
• Finland
  • Helsinki, Finland
    • Helsinki University Hospital and University of Helsinki
• Norway
  • Oslo, Norway
    • Akerhus University Hospital
• Sweden
  • Lund, Sweden
    • Skåne University Hospital
  • Stockholm, Sweden
    • Karolinska Institute

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Luminal Crohn's disease defined according to standardized diagnostic criteria.
• Age ≥ 18 years.
• IFX induction treatment week 0, 2, 6 followed by maintenance therapy.
• IFX treatment length minimum 12 months. Episodic therapy with IFX pause > 12 weeks is not accepted within the last year. The treatment interval in the last three months has to be of 6-10 weeks.

• Complete remission defined as:

  • CDAI score < 150 and
  • Biochemical remission, and
  • No other signs of disease activity as evaluated by endoscopic examination or by magnetic resonance imaging (MRI).
• Stable remission, judged by the treating physician, at two consecutive treatments visits corresponding 2 scheduled IFX infusions. Thus, the first visit is during IFX maintaining therapy (screening visit). The second visit is at time of inclusion corresponding time of next scheduled IFX infusion (i.e. after ≈ 8 weeks).
• No use of oral steroids within 3 months prior to inclusion.
• Concomitant therapy with other immune suppressants, except steroids, is allowed. The dosage and frequency must have been stable three months prior to inclusion and must remain stable throughout the study period.

Exclusion Criteria:

• Initial indication for IFX being predominantly fistulizing perianal disease.
• Any contraindications for continuing IFX treatment, including prior acute or delayed infusion reaction to a TNF- inhibiting agent, any active infection requiring parenteral or oral antibiotic treatment, known infection with tuberculosis, human immunodeficiency virus (HIV) or hepatitis virus.
• Any condition including physician finds incompatible with participation in the study or the patient being unwilling or unable to follow protocol requirements.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: infliximab; Patients in this arm are randomized to continue IFX therapy at an unchanged dosage and frequency.	Drug: Infliximab; Other Names: Remicade
Placebo Comparator: Placebo; Patients in this arm are randomized to receive matching placebo.	Other: Placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Time to relapse after discontinuation of IFX	Relapse defined as CDAI >150 and an increase in CDAI from baseline >70 over 2 consecutive weeks (or definitive relapse as judged by treating physician)	48 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Time to loss of remission	Loss of remission defined as CDAI > 150	48 weeks
Proportion of patients who maintain clinical remission	Defined as CDAI<150	48 weeks
Proportion of patients who maintain clinical and endoscopic remission	Defined as CDAI<150 and SES-CD ≤ 2	48 weeks
Proportion of patients who experience relapse (more stringent definition)	Relapse defined as CDAI >150 and an increase in CDAI from baseline >100 over 2 consecutive weeks (or definitive relapse as judged by treating physician)	48 weeks
Proportion of patients who experience relapse	Relapse defined as CDAI >150 and an increase in CDAI from baseline >70 over 2 consecutive weeks (or definitive relapse as judged by treating physician)drug therapy.	48 weeks

Collaborators and Investigators

• Sponsor: Copenhagen University Hospital at Herlev
• Investigators: Principal Investigator: Mark Ainsworth, MD.PHD.,DMSc, Herlev Hospital, dep. of gastroenterology medical section.

Publications and helpful links

General Publications

• Buhl SS, Steenholdt C, Brynskov J, Thomsen OO, Bendtzen K, Ainsworth MA. Discontinuation of infliximab therapy in patients with Crohn's disease in sustained complete remission (the STOP IT study): protocol for a double-blind, randomised, placebo-controlled, multicentre trial. BMJ Open. 2014 Dec 18;4(12):e005887. doi: 10.1136/bmjopen-2014-005887.

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2013
• Primary Completion (Actual): May 1, 2020
• Study Completion (Actual): May 1, 2020

Study Registration Dates

• First Submitted: August 29, 2012
• First Submitted That Met QC Criteria: March 20, 2013
• First Posted (Estimate): March 25, 2013

Study Record Updates

• Last Update Posted (Actual): March 24, 2022
• Last Update Submitted That Met QC Criteria: March 9, 2022
• Last Verified: March 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Digestive System Diseases; Gastrointestinal Diseases; Gastroenteritis; Intestinal Diseases; Inflammatory Bowel Diseases; Crohn Disease; Antirheumatic Agents; Gastrointestinal Agents; Dermatologic Agents; Infliximab
• Other Study ID Numbers: 02MA