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Completed

NCT Number: NCT02600143

Identification of Predictive Parameters for Colitis in Melanoma Patients Treated With Immunotherapy.

The aim of this trial is to identify biomarkers and genetic predisposition for the development of immune checkpoint related colitis.

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Key information

About this study

Immunotherapy with immune checkpoint-inhibitors is standard treatment for patients with melanoma. However, in about 15% of patients treated with Ipilimumab a grade 3-4 colitis will occur. In programmed cell death protein 1 (PD1) inhibitors colitis is also seen as adverse event, although less prominent. We want to find a good predictive biomarker to select patients that are prone to colitis.So far no test is available that might be predictive whether a patient will develop a grade 3-4 colitis.

The study will consists of four parts: 1.) to identify a genetic profile associated with ipilimumab-induced colitis, 2.) to identify predictive (serum or fecal) biomarkers for ipilimumab-induced colitis, 3.) to study the tissue of ipilimumab-induced colitis and 4) to study the role of the gut microbiome in the development of colitis. Patients are able to participate in one, or more parts of the study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with melanoma who will be treated with immune checkpoint inhibitors (ipilimumab, nivolumab, pembrolizumab)
  • Signed written informed consent.
  • Able to comply with the protocol.

Exclusion criteria

  • Patients with a pre-existing colitis (e.g. Crohn's disease, ulcerative colitis).

Treatment and study plan

Primary outcomes

  1. Genetic predisposition for immunotherapy-induced colitis

    Time frame: 1 week

    Difference in genetic profile on 99 confirmed inflammatory bowel disease (IBD) loci between patients who develop immunotherapy-induced colitis and who do not.

Secondary outcomes

  1. Predictive biomarkers for immunotherapy-induced colitis in stool and serum

    Time frame: Day 0, 21, 42, 63

    Comparison of calprotectin levels in the stool and serum-levels of C reactive protein (CRP), endotoxin, citrulline, intestinal fatty acid-binding protein (I-FABP), calprotectin and interleukin 8 (IL8) between patients who develop immunotherapy-induced colitis and who do not.

  2. Clinical scoring system of colitis

    Time frame: Day -7 to 85

    Prediction of (severity of) colitis based on symptomatology measured with the MAYO score and BRISTOL stool scale.

  3. Histological assessment of colon biopsies in patients that develop colitis

    Time frame: 1 day

    Immunotherapy-induced colitis will be assessed in colon biopsies when a sigmoidoscopy has to be performed for diagnostic reasons.

  4. Analysis of the gut microbiome in stool samples

    Time frame: Day 0, 21, 42, 63

    Microbiome analysis in stool collected before treatment and at 3, 6, and 9 weeks and correlation with development of immunotherapy-induced colitis.

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Registry information

Acronym: COLIPI

Important dates

Study start
2013
Primary completion
2019
Study completion
2019
First posted
Nov 9, 2015
Registry last updated
May 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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