Predicting Response to Standardized Pediatric Colitis Therapy

Phase 4

Completed

Conditions: Ulcerative Colitis

Interventions: Drug: Mesalazine
Drug: IV Corticosteroid
Drug: Oral Corticosteroids
Other: Additional Therapies
Procedure: Colectomy

Registration Number: NCT01536535

Lead Sponsor: Connecticut Children's Medical Center

Brief Summary: This is a multi-center, open-label study to determine the safety and effectiveness (how well it works) of two standardized treatments called "mesalamine" (Pentasa®) and "prednisone" in children with newly diagnosed Ulcerative Colitis (UC). Standardized treatments are types of treatments agreed upon and used by many qualified doctors. The medications being used in this study are considered "standard of care". Currently the ways in which these medicines are used (doses, frequency of dosing) may vary from site to site. This study will determine response to a standardized way of giving these medicines.

This study will also identify biomarkers for ulcerative colitis. Biomarkers are things that doctors can find in blood, stool, or bowel tissue that indicate how much inflammation there is in the bowel, how the inflammation is produced, and whether the inflammation is responding to treatment. Collecting response and remission (free of symptoms) information on these standardized treatments and the "biomarkers" can possibly help doctors create a model, or plan to know which children with UC may respond quickly, or which children may develop complications.

Detailed Description: Ulcerative Colitis (UC) denotes a phenotype of chronic inflammatory bowel disease (IBD), where inflammation is localized to the colonic mucosa, and extends from the rectum proximally in varying extents. The disorder is thought to result from an inappropriate activation of the mucosal immune system by antigens derived from both the host epithelium and the enteric flora, in genetically susceptible individuals. UC is strikingly heterogeneous with respect to age of onset, anatomical extent and disease course, with some experiencing chronically active severe disease, while others have intermittent periods of clinical remission and disease exacerbation. Patients' therapeutic responses vary. The reasons underlying such variability are not well understood. Although it has been widely hypothesized that several genes may influence the development of UC, and modify its phenotypic expression and severity, to date there are few confirmed examples of such relationships.

It has been postulated that the 5-aminosalicylate drugs exert their anti-inflammatory effect locally at the intestinal mucosa. Mechanisms likely include inhibition of 5-lipoxygenase resulting in decreased production of leukotriene B4, scavenging of reactive oxygen metabolites, prevention of up-regulation of leukocyte adhesion molecules, and inhibition of Interleukin 1 (IL-1) synthesis. Though multiple studies have shown the efficacy of aminosalicylates in inducing and maintaining remission in adults with UC, there are few data in children.

Corticosteroids (CS) have been the mainstay of treatment of severe UC since efficacy was first demonstrated in the 1955 randomized controlled trial by Truelove and Witts. Recent practice guidelines developed in adults support their use because of rapid onset of action and significant efficacy though CS dependency is noted. Though no controlled data on their use have been reported in children they are frequently used in this population. A recent report from investigators leading the prospective Pediatric IBD Collaborative Research Group Registry described 97 subjects with a diagnosis of UC and a minimum of 1 year follow-up; 79% received CS. At diagnosis 81% of CS treated patients had moderate/severe disease, and 81% had pancolitis. Clinically inactive disease, determined by physician global assessment, was noted in 60% at 3 months following CS therapy, but by one year 45% were considered CS dependent despite the frequent use of immunomodulators (IM). Among those children with initially moderate to severe disease in clinical remission at 3 months, about two-thirds had stopped the CS by one year.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 431

Inclusion Criteria

Age ≥ 4years and ≤17 years at initiation of therapy (achieved 4th birthday, not yet 18th)
Weight ≥15 kg
New diagnosis of ulcerative colitis established by standard clinical, endoscopic, and histologic features at the PROTECT study site
Colitis extending beyond the rectosigmoid (Paris classification E2, E3, or E4)[144]. If a patient is seriously ill and the clinician does not advance the colonoscope beyond the sigmoid colon but the clinical condition of the patient highly suggests more extensive disease then that patient is eligible for study.
Disease activity by PUCAI of ≥10 at diagnosis
No therapy previously initiated to treat the newly diagnosed ulcerative colitis
Stool culture negative for routine enteric pathogens (Salmonella, Shigella, Campylobacter, E. coli 0157:H7) and Clostridium difficile toxin. Recent successful treatment for Clostridium difficile does not exclude a patient if toxin now absent. However, the patient must be a minimum of 5 weeks from the time treatment was started at the time toxin is absent.
Stool study negative for enteric parasites (ova and parasites)
Parent/guardian consent and patient assent
Ability to remain in follow-up for a minimum of one year from diagnosis
Female patients of child bearing age must have a negative urine pregnancy test and practice acceptable contraception (e.g., abstinence, intramuscular or hormonal contraception, two barrier methods (e.g., condom, diaphragm, or spermicide), intrauterine device, verbal report of the partner with history of vasectomy, or be surgically sterile). All female patients of childbearing potential (post-menarche) will undergo urine pregnancy testing at screening and must not be lactating.

Exclusion Criteria

Clinical, endoscopic, radiologic, or histologic evidence suggesting Crohn's disease (CD) consistent with Paris and North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) criteria [144, 145]
A previous diagnosis of inflammatory bowel disease for which treatment was given
Evidence of any active enteric infection at the time of study entry
Use of any oral CS for non-gastrointestinal indication within the past 4 weeks (e.g., asthma). Use of inhaled CS does not exclude a patient.
History of use of IM or anti-TNFα agent for other medical conditions (e.g., juvenile rheumatoid arthritis) within the past 6 months
Use of Accutane within the past 4 weeks
Use of any investigational drug within the past four weeks
Use of any 5-aminosalicylate within the past 4 weeks
Pregnancy
Subjects with poorly controlled medical conditions (e.g. diabetes, congestive heart failure)
Proctitis or proctosigmoiditis only (Paris classification E1) on colonoscopic evaluation
Chronic renal disease (BUN and serum creatinine >1.5 times the upper normal limit)
Hepatic disease (AST or Alkaline phosphatase (ALP) greater than 3 times the upper normal limit in the absence of concomitant liver disease associated with IBD following full evaluation)
History of allergy or hypersensitivity to salicylates, aminosalicylates, or any component of the Pentasa capsule.
History of coexisting chronic illness or evidence of significant organic or psychiatric disease on medical history or physical examination, which, in the Investigator's opinion, would prevent participation in the study
History or presence of any condition causing malabsorption or an effect on gastrointestinal (GI) motility, or history of extensive small bowel resection (greater than half the length of the small intestine).
The finding of Helicobacter pylori at the time of evaluation does not exclude the patient from the study. Whether to treat this patient for Helicobacter pylori and when will be left to the discretion of the site.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Mild UC	Oral Corticosteroids	Mild = Initiated on mesalazine, or on oral CS with Pediatric Ulcerative Colitis Activity Index (PUCAI) \< 45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-Tumour Necrosis Factor alpha (TNFα) therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-MP at 1-1.5 mg/kg/day Colectomy
Mild UC	IV Corticosteroid	Mild = Initiated on mesalazine, or on oral CS with Pediatric Ulcerative Colitis Activity Index (PUCAI) \< 45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-Tumour Necrosis Factor alpha (TNFα) therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-MP at 1-1.5 mg/kg/day Colectomy
Moderate to Severe UC	Additional Therapies	Moderate/Severe = Initiated on IV CS, or oral CS with PUCAI ≥45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-TNFα therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-Mercaptopurine (MP) at 1-1.5 mg/kg/day Colectomy
Moderate to Severe UC	Colectomy	Moderate/Severe = Initiated on IV CS, or oral CS with PUCAI ≥45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-TNFα therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-Mercaptopurine (MP) at 1-1.5 mg/kg/day Colectomy
Mild UC	Additional Therapies	Mild = Initiated on mesalazine, or on oral CS with Pediatric Ulcerative Colitis Activity Index (PUCAI) \< 45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-Tumour Necrosis Factor alpha (TNFα) therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-MP at 1-1.5 mg/kg/day Colectomy
Mild UC	Colectomy	Mild = Initiated on mesalazine, or on oral CS with Pediatric Ulcerative Colitis Activity Index (PUCAI) \< 45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-Tumour Necrosis Factor alpha (TNFα) therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-MP at 1-1.5 mg/kg/day Colectomy
Moderate to Severe UC	IV Corticosteroid	Moderate/Severe = Initiated on IV CS, or oral CS with PUCAI ≥45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-TNFα therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-Mercaptopurine (MP) at 1-1.5 mg/kg/day Colectomy
Moderate to Severe UC	Oral Corticosteroids	Moderate/Severe = Initiated on IV CS, or oral CS with PUCAI ≥45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-TNFα therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-Mercaptopurine (MP) at 1-1.5 mg/kg/day Colectomy
Mild UC	Mesalazine	Mild = Initiated on mesalazine, or on oral CS with Pediatric Ulcerative Colitis Activity Index (PUCAI) \< 45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-Tumour Necrosis Factor alpha (TNFα) therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-MP at 1-1.5 mg/kg/day Colectomy
Moderate to Severe UC	Mesalazine	Moderate/Severe = Initiated on IV CS, or oral CS with PUCAI ≥45 Patients can be treated with any of the therapies noted below: Mesalazine: doses is rounded to the nearest 500mg increment, maximum dose of 75 mg/kg/day Oral corticosteroids:1-1.5 mg/kg/day, rounded up to the nearest 5 mg value IV corticosteroids: Additional Therapies: Calcineurin inhibitor (cyclosporine, tacrolimus) or anti-TNFα therapy: These therapies may also be instituted if in the judgment of the attending physician is needed. Immunomodulator or biologic therapy: thiopurine then dosing of azathioprine:2.5-3 mg/kg/day; 6-Mercaptopurine (MP) at 1-1.5 mg/kg/day Colectomy

Primary Outcome Measures

Name	Time	Method
Number of Participants Who Needed Additional Therapy or Colectomy	Within 52 weeks	Number of participants who needed additional therapy or colectomy. Additional therapy included Anti-Tumour Necrosis Factor alpha (TNFα), Calcineurin inhibitor, Immunomodulator
Number of Participants With Corticosteroid Free Remission (SFR)	52 weeks	Week 52 CS-free remission: Number of participants with a PUCAI \< 10 and no corticosteroids (CS) for 28 days without additional therapy or colectomy. Participants in both groups received corticosteroids, biologics, or colectomies, if symptomatic. The Pediatric Ulcerative Colitis Activity Index (PUCAI) is a non-invasive disease activity index. The index measures include abdominal pain, rectal bleeding, stool consistency, number of stools per 24 hours, nocturnal stools, and activity level. A total score less than 10 indicates remission, Mild disease activity is 10-30, Moderate 35-60, Severe disease activity 65-85.

Secondary Outcome Measures

Name	Time	Method
Number of Participants Receiving a Colectomy	Within 52 weeks	Number of participants who received a colectomy within 52 weeks

Trial Locations

Locations (29): Children's Hospital of Boston
🇺🇸
Boston, Massachusetts, United States
Monroe Carell Jr. Children's Hospital at Vanderbilt
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Nashville, Tennessee, United States
Emory Children's Center
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Atlanta, Georgia, United States
Mt Sinai Hospital
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New York, New York, United States
Golisano Children's Hospital SUNY Upstate Medical University
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Syracuse, New York, United States
Children's Hospital of Eastern Ontario
🇨🇦
Ottawa, Ontario, Canada
Nationwide Children's Hospital
🇺🇸
Columbus, Ohio, United States
Riley Children's Hospital
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Indianapolis, Indiana, United States
Morgan Stanley Children's Hospital
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New York, New York, United States
University of Minnesota Medical Center
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Minneapolis, Minnesota, United States
Ann & Robert H. Lurie Children's Hospital of Chicago
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Chicago, Illinois, United States
University of California at San Francisco
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San Francisco, California, United States
UCLA Medical Center
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Los Angeles, California, United States
John Hopkins Children's Hospital
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Baltimore, Maryland, United States
Goryeb Children's Hospital / Atlantic Health
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Morristown, New Jersey, United States
Cohen Children's Medical Center
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New Hyde Park, New York, United States
University of North Carolina at Chapel HIll
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Chapel Hill, North Carolina, United States
Cincinnati Children's Hospital Medical Center
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Cincinnati, Ohio, United States
Women and Children's Hospital of Buffalo
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Buffalo, New York, United States
Hospital for Sick Children
🇨🇦
Toronto, Ontario, Canada
Children's Hospital of Pittsburgh of UPMC
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Pittsburgh, Pennsylvania, United States
Children's Hospital of Philadelphia
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Philadelphia, Pennsylvania, United States
Primary Children's Medical Center (University of Utah)
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Salt Lake City, Utah, United States
UT Southwestern
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Dallas, Texas, United States
Medical College of Wisconsin
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Milwaukee, Wisconsin, United States
IWK Health Centre
🇨🇦
Halifax, Nova Scotia, Canada
Connecticut Children's Medical Center
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Hartford, Connecticut, United States
Nemours Children's Clinic
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Jacksonville, Florida, United States
Hasbro Children's Hospital
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Providence, Rhode Island, United States