Advanced Solid Tumor
Conditions
Keywords
Immune Checkpoint Inhibitor, Microbiome, Immune-Mediated Toxicity
Brief summary
The composition of the gut microbiome has been associated with response and the development of toxicities on immune checkpoint inhibitors (ICIs) in multiple tumor types. The aim of this study is to examine the gut microbiome composition in patients undergoing standard of care treatment for advanced/unresectable and/or metastatic solid tumors with ICIs. Fecal samples and peripheral blood samples will be collected to further characterize the diversity of gut bacteria and to study potential mechanisms by which gut bacteria impact the immune response.
Detailed description
This is a prospective study of gut microbial markers. Patients with histologically confirmed advanced/unresectable or metastatic solid tumors who are planned to initiate standard of care ICIs or are undergoing standard of care treatment with ICIs will be approached for participation in the study.
Interventions
None listed
Sponsors
Princess Margaret Hospital, Canada
University of Toronto
Sunnybrook Health Sciences Centre
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Sign written and voluntary informed consent * Adult patients aged \>=18, male or female * Eastern Cooperative Group (ECOG) performance status 0-2 * Histologic diagnosis of an advanced/unresectable or metastatic solid tumor * Measurable disease as per RECIST 1.1 criteria * Be suitable for or receiving ICI treatment * Prior immunotherapy allowed * Be willing and able to provide fecal and blood specimens for analysis as per protocol
Exclusion criteria
* Subjects with a history of inflammatory bowel disease, chronic diarrhea or malabsorption syndromes and significant prior bowel resection as judged by the study investigator
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Relative abundance and composition of immunotherapy response-associated bacterial species in patients with advanced/unresectable or metastatic solid tumors | 6 months | Fecal microbial composition analyzed by 16S rRNA and metagenomic sequencing |
| Relative abundance and composition of immunotherapy toxicity-associated bacterial species in patients with advanced/unresectable or metastatic solid tumors | 12 months | Fecal microbial composition analyzed by 16S rRNA and metagenomic sequencing; IgA sequencing of fecal samples from patients who develop diarrhea/colitis |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the composition of the intestinal microbiome induced by ICIs | 6 months | Fecal microbial composition analyzed by 16S rRNA and metagenomic sequencing |
| Relative abundance of bacterial DNA in peripheral blood samples | 6 months | Blood microbial abundance measured via qPCR |
| Changes in immune cell subsets in the systemic circulation upon progression on ICIs correlated with changes in microbiome composition | 2 years | Flow cytometry of blood at baseline and at development of progressive disease and analysis of microbiome composition at baseline and at development of progressive disease |
| Identification of serum metabolites in systemic circulation and correlation with intestinal microbiome composition | 6 months | Analysis of serum metabolites using chromatography coupled to tandem mass spectrometry |
Countries
Canada
Contacts
Primary ContactRossanna C. Pezo, MD/PhD
Outcome results
None listed