Efficacy of Vedolizumab in Crohn's Disease Patients Naive to Biological Therapy

Crohn Disease Clinical Trial

Official title:

Efficacy of Vedolizumab in Crohn's Disease Patients Naive to Biological Therapy: a Brazilian Multicentric Observational Real-world Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04362735
• Other study ID #: IISR-2020-103104
• Status: Not yet recruiting
• Start date: August 1, 2020
• Est. completion date: April 1, 2021

Study information

• Verified date: April 2020
• Source: Pontifícia Universidade Católica do Paraná
• Contact: Paulo Kotze, phd
• Phone: +5541996648989
• Email: pgkotze[@]hotmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

INTRODUCTION: Vedolizumab is a gut selective anti-integrin agent which binds to the alfa4beta7 integrin, preventing its coupling to the endothelial MadCAM-1. It reduces leucocyte trafficking from the endothelium consequently reducing intestinal tissue inflammation. There is scarce evidence on the use of vedolizumab in CD in Brazil, mostly in patients with no previous biological therapy, where the drug seems to have a more adequate therapeutic potential.

Tha primary aim of the study is to analyze clinical remission rates at weeks 12, 26 and 52, and at last follow-up on naive CD patients submitted to vedolizumab therapy. Secondary outcomes will be clinical response rates at weeks 12, 26 and 52, and at last follow-up; endoscopic remission rates in colonoscopies performed; persistence of drug therapy over time; adverse events during treatment with vedolizumab and rates of abdominal surgery during therapy.

METHODS: A retrospective, longitudinal, observational study will be performed with patients with CD who used Vedolizumab at any time of their treatment as the first biologic option, after failure of conventional therapy. Following the induction dose of 300 mg at weeks 0, 2 and 6, and maintenance of 300 mg every 8 weeks, patients will be followed up to 52 weeks (1 year) or more (last follow-up captured). Records of the clinical evaluations at week 12, 26 and 52, and last follow-up, will be checked according to the HBI and PGA to define clinical response or clinical remission. Colonoscopies will also be checked to evaluate mucosal healing. Electronic charts will be reviewed also to analyze adverse events and surgery during therapy.

Description:

INTRODUCTION: Inflammatory bowel diseases (IBD) are a group of chronic, idiopathic and immune-mediated diseases, mainly represented by Crohn's disease (CD) and Ulcerative Colitis (UC). There is a broad therapeutic spectrum according to the degree of disease activity, extension and behavior, from aminosalicylates to biological therapy. Tumor necrosis factor (TNF) alpha inhibitors were the first class of biological therapy approved for IBD. However, some patients do not respond to treatment (primary non-responders) or lose response over time (secondary loss of response). With a different mechanism of action, the class of anti-integrin monoclonal antibodies, represented by natalizumab and vedolizumab, has recently expanded. Vedolizumab is a gut selective anti-integrin that binds to the alfa4beta7 integrin, preventing its coupling to the endothelial MadCAM-1. In this way, it reduces the process of lymphocyte migration and reduces intestinal tissue inflammation. Multicentric real life studies with vedolizumab in UC and CD showed the efficacy and safety of the drug. More recently, a head-to-head trial comparing the efficacy of vedolizumab against adalimumab in UC demonstrated superiority of vedolizumab in comparison to the subcutaneous anti-TNF agent, defining positioning of the drug as an adequate first option in therapeutic sequencing. There is no head to head trial comparing vedolizumab against other agents in CD. Indeed, there is a lack of studies on the use of vedolizumab in CD in Brazil, mostly in biologic naïve patients, where the drug seems to have a more adequate therapeutic potential.

OBJECTIVES:

1. Primary objective: to analyze clinical remission rates [defined as a Harvey-Bradshaw index (HBI) of equal or lower than 4 for Crohn's disease (CD)] at weeks 12, 26 and 52, and at last follow-up.

2. Secondary objectives: to analyze clinical response rates (defined as a reduction at the HBI of equal or more than 3 points for CD and according to physician global assessment - PGA) at weeks 12, 26 and 52, and at last follow-up; to analyze endoscopic remission rates (defined as absence of ulcers in CD) in colonoscopies performed; to analyze persistence of drug therapy over time; to analyze adverse events during treatment with vedolizumab and rates of abdominal surgery during therapy.

METHODS: This project is already approved by the Institutional Review Board (IRB) from the Catholic University of Paraná, Brasil. A retrospective, longitudinal, observational study will be performed with patients with CD who used Vedolizumab at any time of their treatment as the first biologic option, after failure of conventional therapy. Inclusion criteria: Patients with CD, who used vedolizumab as the first biological agent during medical treatment, after failure of conventional therapy (aminosalicylates, steroids and/or immunomodulators such as azathioprine and methotrexate). Exclusion criteria: Patients with UC, other causes of intestinal inflammation (ischemic or infectious colitis, for example) non-IBD related, IBD-undetermined not defined as CD or UC will be excluded from the analysis. Patients with vedolizumab who had previous exposure to anti-TNF agents will also be excluded. Pregnant and pediatric patients (less than 18 years old) will also be excluded. Following the induction dose of 300 mg at weeks 0, 2 and 6, and maintenance of 300 mg every 8 weeks, patients will be followed up to 52 weeks (1 year) or more (last follow-up captured). Records of the clinical evaluations at week 12, 26 and 52, and last follow-up, will be checked according to the HBI for CD, and PGA to define clinical response or clinical remission. Colonoscopies will also be checked to evaluate mucosal healing.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: April 1, 2021
• Est. primary completion date: January 20, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with CD (any location)who used vedolizumab as the first biological agent during medical treatment, after failure of conventional therapy (5-ASA, steroids and/or immunomodulators such as azathioprine and methotrexate).

Exclusion Criteria:

• Patients with UC

• Patients with other causes of intestinal inflammation (ischemic or infectious colitis, for example) non-IBD related

• Patients with IBD-undetermined not defined as CD or UC

• Patients with vedolizumab who had previous exposure to anti-TNF agents

• Pregnant patients

• Pediatric patients (less than 18 years old)

Related Conditions & MeSH terms

• Crohn Disease

Intervention

Drug:
• Vedolizumab
Vedolizumab 300 mg at weeks 0, 2 and 6 as induction. Maintenance every 4 or 8 weeks, as on-label recommendations.

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Pontifícia Universidade Católica do Paraná	Takeda

References & Publications (3)

Kopylov U, Verstockt B, Biedermann L, Sebastian S, Pugliese D, Sonnenberg E, Steinhagen P, Arebi N, Ron Y, Kucharzik T, Roblin X, Ungar B, Shitrit AB, Ardizzone S, Molander P, Coletta M, Peyrin-Biroulet L, Bossuyt P, Avni-Biron I, Tsoukali E, Allocca M, K — View Citation

Perin RL, Damião AOMC, Flores C, Ludvig JC, Magro DO, Miranda EF, Moraes AC, Nones RB, Teixeira FV, Zeroncio M, Kotze PG. VEDOLIZUMAB IN THE MANAGEMENT OF INFLAMMATORY BOWEL DISEASES: A BRAZILIAN OBSERVATIONAL MULTICENTRIC STUDY. Arq Gastroenterol. 2019 S — View Citation

Schreiber S, Dignass A, Peyrin-Biroulet L, Hather G, Demuth D, Mosli M, Curtis R, Khalid JM, Loftus EV Jr. Systematic review with meta-analysis: real-world effectiveness and safety of vedolizumab in patients with inflammatory bowel disease. J Gastroentero — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical remission	HBI index = 4	12 weeks
Primary	Clinical remission	HBI index = 4	26 weeks
Primary	Clinical remission	HBI index = 4	52 weeks
Secondary	Clinical response	reduction in HBI index = 3 points + PGA	12 weeks
Secondary	Clinical response	reduction in HBI index = 3 points + PGA	26 weeks
Secondary	Clinical response	reduction in HBI index = 3 points + PGA	52 weeks
Secondary	Mucosal healing	absence of ulcers at colonoscopy	through study completion, an average of 52 weeks
Secondary	Need for major surgery during treatment	Any major abdominal surgery during therapy with vedolizumab	through study completion, an average of 52 weeks