Probiotics for the Prevention of Immunotherapy Induced Colitis in Patients Receiving Immunotherapy

Description

The clinical trial tests the use of over-the-counter probiotics VSL#3® 450B in patients receiving immunotherapy. Immunotherapy with monoclonal antibodies, helps the body's immune system attack tumor cells, and interferes with the ability of tumor cells to grow and spread. Immunotherapy can also cause an unfortunate side effect of inflammation of the colon and diarrhea, also known as immune checkpoint inhibitor induced colitis. Immune checkpoint inhibitor induced colitis can occur in up to 45% of patients receiving immunotherapy. Taking probiotics VSL#3® 450B may reduce the chances of developing immune checkpoint inhibitor induced colitis in patients receiving immunotherapy.

Conditions

Malignant Solid Neoplasm

Study Overview

Study Details

Study overview

The clinical trial tests the use of over-the-counter probiotics VSL#3® 450B in patients receiving immunotherapy. Immunotherapy with monoclonal antibodies, helps the body's immune system attack tumor cells, and interferes with the ability of tumor cells to grow and spread. Immunotherapy can also cause an unfortunate side effect of inflammation of the colon and diarrhea, also known as immune checkpoint inhibitor induced colitis. Immune checkpoint inhibitor induced colitis can occur in up to 45% of patients receiving immunotherapy. Taking probiotics VSL#3® 450B may reduce the chances of developing immune checkpoint inhibitor induced colitis in patients receiving immunotherapy.

Probiotics Preventing Immune Checkpoint Inhibitor-Induced Colitis

Probiotics for the Prevention of Immunotherapy Induced Colitis in Patients Receiving Immunotherapy

Condition
Malignant Solid Neoplasm
Intervention / Treatment

-

Contacts and Locations

Jacksonville

Mayo Clinic in Florida, Jacksonville, Florida, United States, 32224-9980

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Male or female age ≥ 18 years
  • * Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
  • * Histologically confirmed solid malignancy
  • * Will be starting on ICIs
  • * For cohort 1: Ipilimumab with or without anti-PD-1/PD-L1 including but not limited to pembrolizumab, nivolumab, cemiplimab, atezolizumab, avelumab, or durvalumab
  • * For cohort 2: Anti-PD-1/PD-L1 described above with or without chemotherapy
  • * Absolute neutrophil count (ANC) ≥ 1000/mm\^3
  • * Platelet count ≥ 75,000/mm\^3
  • * Hemoglobin ≥ 9.0 g/dL
  • * Creatinine ≤ 2 x upper limit of normal (ULN)
  • * Serum glutamic-oxaloacetic transaminase (SGOT) \[aspartate transaminase (AST)\] ≤ 2 x ULN
  • * Albumin ≥ 3 g/dL
  • * Willing and able to provide research stool and blood samples
  • * Negative serum pregnancy test done ≤ 7 days prior to enrollment, for women of childbearing potential only
  • * Capable of providing valid informed consent
  • * Willing to return to enrolling institution for all study visits (blood draws, etc)
  • * Requires prolonged systemic antibiotic therapy for other condition and recent systemic antibiotic within the past 2 weeks
  • * Fecal microbiota transplant (FMT) within the past 6 months
  • * FMT with an associated serious adverse event related to the FMT product or procedure
  • * Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of over-the-counter probiotics
  • * Immunocompromised patients including patients known to be HIV positive or those on chronic steroids \> 20 mg prednisone a day or prednisone-equivalent Note: Must be off systemic steroids at least 90 days prior to enrollment. However, topical steroids, inhalants or steroid eye drops are permitted
  • * History of inflammatory bowel disease (IBD), e.g., ulcerative colitis, Crohn's disease, or microscopic colitis
  • * History of chronic diarrhea
  • * History of celiac disease
  • * Currently has a colostomy
  • * Intraabdominal surgery related to gastrointestinal tract within the last 60 days
  • * Evidence of active, severe colitis
  • * History of short gut syndrome or motility disorders
  • * Requires the regular use of medications to manage bowel hypermotility
  • * Active autoimmune disease that has required systemic treatment in the ≤ 30 days (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive drugs) prior to randomization. Note: Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment. Patients with vitiligo, Graves' disease, or psoriasis not requiring systemic treatment within the past 30 days are not excluded

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Mayo Clinic,

Saranya Chumsri, M.D., PRINCIPAL_INVESTIGATOR, Mayo Clinic

Study Record Dates

2027-08-30