The Effects of Probiotics on Intestinal Permeability in Gastrointestinal Cancer Patients in Chemotherapy
Primary Purpose
Intestinal Permeability, Gastrointestinal Irritation, Mucositis
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Probiotic
Sponsored by
About this trial
This is an interventional treatment trial for Intestinal Permeability
Eligibility Criteria
Inclusion Criteria:
- GI cancer (all types) patients undergoing chemotherapy in oncologic department at Rigshospitalet in Copenhagen
- Age >18 years
- Patients with at least three planned chemo therapy sessions left
Exclusion Criteria:
- Pregnant
- Patients who don't speak, write or understand Danish
- Known inflammatory bowel diseases or malabsorption
- Chronic kidney disease (2 x upper limit plasma creatinine)
- Neutropenia (< 1.5 x 109/L neutrophilic granulocytes in peripheral blood)
- Use of antibiotics
- Use of lactulose (laxative) and not able to discontinue three days prior to urin collection (lactulose/mannitol test)
- Use of probiotics
Sites / Locations
- Departmen of Oncology, Rigshospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
probiotic treatment
Arm Description
Probiotic: VSL#3 is a probiotic formula containing a mixture of 9x10^10 CFU/g Lactobacilli strains (Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus casei, and Lactobacillus bulgaricus), 8x10^10 CFU/g Bifidum strains (Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis) and 20x10^10 CFU/g Streptococcus thermophilus. Administred orally
Outcomes
Primary Outcome Measures
Intestinal permeability
Urinary lactulose-mannitol test
Secondary Outcome Measures
Gastrointestinal adverse events
Diarrhea, abdominal pain, abdominal cramps, constipation, etc.
Full Information
NCT ID
NCT03704727
First Posted
October 10, 2018
Last Updated
April 17, 2019
Sponsor
University of Copenhagen
Collaborators
Actial Farmaceutica S.r.l., Nutricia, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT03704727
Brief Title
The Effects of Probiotics on Intestinal Permeability in Gastrointestinal Cancer Patients in Chemotherapy
Official Title
The Effects of Probiotics on Intestinal Permeability in Gastrointestinal Cancer Patients in Chemotherapy
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
February 1, 2019 (Actual)
Study Completion Date
February 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Copenhagen
Collaborators
Actial Farmaceutica S.r.l., Nutricia, Inc.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The aim of this study is to test the hypothesis that adjuvant administration of probiotics in cancer patients undergoing chemotherapy can reduce a chemo-induced increased intestinal permeability. Furthermore, we hypothesize that the use of probiotics may reduce the occurrence of gastrointestinal side effects such as diarrhea, abdominal pains, bacterial translocation and infections following chemotherapy.
Detailed Description
Treatment of most cancer patients involves radiation and/or chemotherapy which often leads to gastrointestinal toxicity. Cytotoxic chemotherapy in particular often induces several intestinal abnormalities such as mucositis including destruction of intestinal villi, alterations in the gut microbiota, modulation of tight junctions, leading to an increased intestinal permeability. These toxic effects have been observed in several types of chemotherapy and different methods of administering chemotherapy.
The intestinal permeability is regulated and protected by a number factors, including a mucus layer covering the surface of the epithelium. This mucus layer is partly regulated by intestinal bacteria. Therefore it is hypothesized that chemoinduced changes in the intestinal microbiota may possibly affect intestinal permeability. Changes in the intestinal microbiota are seen after only one or a few cycles of chemotherapy treatment in different types of cancers, and could possibly be a contributing factor in the development of mucositis.
It is possible that probiotics may interfere with the ability of pathogenic bacteria to bind to the surface of the intestinal epithelial lining. In vitro studies have shown that probiotics may reduce a post-infective (Escherichia coli) increased intestinal permeability, or increased permeability due to incubation with pro-inflammatory cytokines. VSL#3 is a probiotic formula containing a mixture of 9x10^10 CFU/g Lactobacilli strains (Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus casei, and Lactobacillus bulgaricus), 8x10^10 CFU/g Bifidum strains (Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis) and 20x10^10 CFU/g Streptococcus thermophilus. In vitro and ex vivo studies have suggested that the probiotic bacteria found in VSL#3 may have a reducing effect on intestinal permeability as well as a positive modulating effect on tight junction protein expression. Escherichia coli Nissle 1917 is another bacterial strain that has been shown to be able to mediate the modulation of tight junction proteins and thus intestinal permeability. The precise mechanisms behind the effects of probiotics on intestinal epithelial permeability are not yet clear, but some mechanisms have been proposed, including a reduction in bacterial secretion of proinflammatory cytokines as well as other secreted products from probiotic microbial metabolism.
It is not known whether all probiotic strains exert a similar effect on intestinal permeability, as only very limited clinical research has addressed this relation. However, it is very likely that the specific choice of probiotic bacterial species may play a crucial role. We are only familiar with one clinical trial examining the effect of probiotics on intestinal permeability in adults with cancer undergoing treatment in the form of colectomy, but no adjuvant chemotherapy. Probiotics in the form of Lactobacillus plantarum, Lactobacillus acidophilus and Bifidobacterium longum was administered perioperative and postoperative to patients undergoing colectomy, and the study showed that probiotics improved the integrity of the small intestinal mucosal barrier, induced modulation of the intestinal microbiome as well as a reduction in the postoperative rate of infections.The same researchers also measured serum zonulin in the same subjects, and found that the treatment with probiotics also reduced the concentration of postoperative serum zonulin, and thus inhibited the same increase in intestinal permeability as was the case in the control group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intestinal Permeability, Gastrointestinal Irritation, Mucositis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
probiotic treatment
Arm Type
Experimental
Arm Description
Probiotic: VSL#3 is a probiotic formula containing a mixture of 9x10^10 CFU/g Lactobacilli strains (Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus casei, and Lactobacillus bulgaricus), 8x10^10 CFU/g Bifidum strains (Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis) and 20x10^10 CFU/g Streptococcus thermophilus. Administred orally
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic
Intervention Description
Probiotics (beneficial microorganisms) VSL#3 is a probiotic formula containing a mixture of 9x10^10 CFU/g Lactobacilli strains (Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus casei, and Lactobacillus bulgaricus), 8x10^10 CFU/g Bifidum strains (Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis) and 20x10^10 CFU/g Streptococcus thermophilus
Primary Outcome Measure Information:
Title
Intestinal permeability
Description
Urinary lactulose-mannitol test
Time Frame
4 hours
Secondary Outcome Measure Information:
Title
Gastrointestinal adverse events
Description
Diarrhea, abdominal pain, abdominal cramps, constipation, etc.
Time Frame
1 week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
GI cancer (all types) patients undergoing chemotherapy in oncologic department at Rigshospitalet in Copenhagen
Age >18 years
Patients with at least three planned chemo therapy sessions left
Exclusion Criteria:
Pregnant
Patients who don't speak, write or understand Danish
Known inflammatory bowel diseases or malabsorption
Chronic kidney disease (2 x upper limit plasma creatinine)
Neutropenia (< 1.5 x 109/L neutrophilic granulocytes in peripheral blood)
Use of antibiotics
Use of lactulose (laxative) and not able to discontinue three days prior to urin collection (lactulose/mannitol test)
Use of probiotics
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jens R Andersen, MD,MPA
Organizational Affiliation
University of Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Departmen of Oncology, Rigshospital
City
Copenhagen
ZIP/Postal Code
2100 OE
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The Effects of Probiotics on Intestinal Permeability in Gastrointestinal Cancer Patients in Chemotherapy
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