Mucositis Clinical Trial
Official title:
The Effects of Probiotics on Intestinal Permeability in Gastrointestinal Cancer Patients in Chemotherapy
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.
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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02252926 -
Local Anesthetic Treatment of Oral Pain in Patients With Mucositis
|
Phase 2 | |
Completed |
NCT01155609 -
L-lysine in Treating Oral Mucositis in Patients Undergoing Radiation Therapy With or Without Chemotherapy For Head and Neck Cancer
|
N/A | |
Completed |
NCT00357942 -
Topical Morphine for Stomatitis-related Pain Induced by Chemotherapy
|
Phase 4 | |
Completed |
NCT00360685 -
Tacrolimus and Mycophenolate Mofetil (MMF) in GVHD Prophylactic Regimen Compared to Tacrolimus and Methotrexate (MTX
|
N/A | |
Completed |
NCT04586491 -
The Effect of Oral Care Protocol on Prevention of Oral Mucositis in Pediatric Cancer Patients
|
N/A | |
Withdrawn |
NCT02589860 -
Analysis of Oral Mucositis in Patient's Undergoing Melphalan Conditioning and Autologous Stem Cell Transplant
|
||
Not yet recruiting |
NCT02506231 -
The Effect of Folinic Acid Rescue Following MTX GVHD Prophylaxis on Regimen Related Toxicity and Transplantation Outcome
|
Phase 2/Phase 3 | |
Completed |
NCT02639377 -
Efficacy of 0.12% Chlorhexidine Gluconate for Peri-implant Mucositis and Gingivitis
|
Phase 2 | |
Completed |
NCT02605382 -
Efficacy of 0.12% Chlorhexidine Gluconate for Peri-implant Mucositis
|
Phase 2 | |
Terminated |
NCT02575313 -
The Effects of Whole Food Intervention on Mucositis in Patients Treated for Head and Neck Cancer
|
Phase 1/Phase 2 | |
Completed |
NCT00956254 -
Fentanyl Sublingual Spray in Treating Opioid-tolerant Cancer Patients With or Without Oral Mucositis
|
Phase 3 | |
Completed |
NCT00584597 -
A Trial of Homeopathic Medication TRAUMEEL S for the Treatment of Radiation-Induced Mucositis
|
Phase 1 | |
Enrolling by invitation |
NCT05590117 -
Protective Effect of Pentoxifylline Against Chemotherapy Induced Toxicities in Patients With Colorectal Cancer
|
Early Phase 1 | |
Completed |
NCT05635929 -
Oral Mucositis and Quality of Life With a Mucosa Topical Composition in Head & Neck Cancer Patients.
|
N/A | |
Completed |
NCT05181943 -
Effectiveness of Photo-biomodulation in the Treatment of Chemotherapy Induced Mucositis
|
N/A | |
Completed |
NCT03713567 -
Clinical, Immunological and Microbiological Evaluation of Experimental Gingivitis and Peri-implant Mucositis
|
N/A | |
Completed |
NCT02671812 -
Outcome After Dental Implant Treatment
|
||
Terminated |
NCT02273752 -
Pharmacokinetically Guided Everolimus in Patients With Breast Cancer, Pancreatic Neuroendocrine Tumors, or Kidney Cancer
|
Phase 2 | |
Recruiting |
NCT01707641 -
Effect of Lactobacillus Brevis CD2 in Prevention of Radio-chemotherapy Induced Oral Mucositis in Head and Neck Cancer
|
Phase 4 | |
Completed |
NCT01015183 -
Prevention Chemotherapy Induced Mucositis by Zinc Sulfate
|
Phase 2/Phase 3 |