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Gut Microbiota (GM) Biodiversity in Patients With Solid Tumors Treated With Immune Checkpoint Inhibitors (ICIs): a Monocenter Prospective Study to Identify the Interactions Between GM and ICIs (GM&ICI)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Active, not recruiting

Conditions

Solid Tumor Cancer Treatment With Immunotherapy

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Although it is a milestone in the treatment of solid neoplasms, Immunotherapy (ICI) is still burdened by low response rate to the treatment and the occurrence of immune-related adverse events (irAEs). Recently, many studies have suggested that the The diversity of the intestinal microbiota (GM) can modulate response to ICIs [1]. The GM would be able to produce several molecules that can influence the growth of cancer cells and modulate anti-cancer immunity.

Our project aims to investigate changes in the subject and its relationship to immunotherapy.

Dynamic changes in cytokines can be a indicator of increased or decreased toxin translocation bacterial and therefore of the greater or lesser integrity of the barrier intestinal. Define the influence of diet on changes in GM can also help us understand how to modify these factors to improve the outcome of the subject undergoing immunotherapy.

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients aged ≥18 years
  2. Life-expectancy ≥6 months;
  3. All participants have signed the consent form before enrollment
  4. Patients with cancer who have to start immunotherapy with or without chemotherapy/targeted therapy

Exclusion criteria

  1. Patients reporting an intake of antibiotic therapy during the last 30 days (rifaximin therapy used in patients with hepatocellular carcinoma in order to decrease the occurrence of overt Hepatic Encephalopathy is permitted) or any probiotic therapy in the last 30 days
  2. A personal history of autoimmune or inflammatory bowel disease
  3. Any major intestinal surgery (including bariatric surgery) in the previous six months
  4. Ongoing enteral or parenteral nutrition
  5. Patients with psychiatric illness/social situations that would limit compliance with study requirements.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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