Intestinal Microbiome, Oral Microbiome, and Whole Blood Transcriptome Analyses in Gastrointestinal Malignancies

Last updated: January 23, 2025
Sponsor: Viome
Overall Status: Completed

Phase

N/A

Condition

Digestive System Neoplasms

Gastric Ulcers

Colon Cancer; Rectal Cancer

Treatment

N/A

Clinical Study ID

NCT05462314
V130
  • Ages > 18
  • All Genders

Study Summary

The primary objective of this prospective observational study is to characterize the gut and oral microbiome as well as the whole blood transcriptome in gastrointestinal cancer patients and correlate these findings with cancer type, treatment efficacy and toxicity. Participants will be recruited from existing clinical sites only, no additional clinical sites are needed.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Histologic diagnosis of gastrointestinal malignancy including pancreatic,esophageal, gastric, colon, rectal, hepatocellular, or biliary carcinoma.

  • Subjects must have a) newly diagnosed recurrent or metastatic disease b) progressivedisease on second or later line therapies, or c) locally advanced inoperable diseasereceiving palliative therapy.

  • Age > 18 years.

  • Ability to understand and willing to sign a written informed consent document.

Exclusion

Exclusion Criteria:

  • Subjects with gastrointestinal malignancy already receiving treatment includingchemotherapy, immunotherapy, radiation therapy or investigational agents fortreatment of a) newly diagnosed recurrent or metastatic disease b) progressivedisease on second or later line therapies, or c) locally advanced disease.

  • Subjects with gastrointestinal malignancy who will not be receiving cancer directedtherapy including chemotherapy, immunotherapy, radiation therapy or investigationalagents.

  • Subjects with active infectious gastroenteritis.

Study Design

Total Participants: 24
Study Start date:
March 29, 2022
Estimated Completion Date:
January 21, 2025

Study Description

The primary objective of this prospective observational study is to characterize the gut and oral microbiome as well as the whole blood transcriptome in gastrointestinal cancer patients and correlate these findings with cancer type, treatment efficacy and toxicity.

This study will provide biospecimens from a diverse range of gastrointestinal cancer patients to allow preliminary characterization of the diversity and composition of the GIM microbiome and pilot analysis of changes in the microbiome as a function of both treatment and disease progression.

This is a prospective cohort study will characterize and evaluate the microbiome of GIM patients, with various histologies. The investigators plan to enroll 200 patients with a diagnosis of gastrointestinal cancer including pancreatic, esophageal, gastric, colon, rectal, liver and biliary cancers with (i) newly diagnosed recurrent or metastatic disease initiating therapy or (ii) with progressive disease on second or later line therapies, or (iii) with locally advanced, inoperable disease receiving palliative therapy. Stool, blood and saliva samples will be collected at baseline, early in treatment (3-6 weeks), and then at 3 month intervals until progression or intolerable toxicity or up to 36 months.

The results of this study are expected to provide the basis for larger, more focused studies of the microbiome in distinct GIMs and relationship to specific treatment efficacy and toxicity. Ultimately, this classification of the gastrointestinal cancer microbiome may lead to novel risk stratification paradigms, novel treatments and maintenance strategies. Furthermore, this study may lead to improved diagnostics, companion diagnostics, and nutritional interventions for cancer prevention and therapy.

Connect with a study center

  • Icahn School of Medicine at Mount Sinai

    New York, New York 10029
    United States

    Site Not Available

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