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Recruiting

NCT Number: NCT04957511

Gut Microbiome and Treatment for Gynecological Cancer Patients Receiving Immunotherapy

30 participants with advanced or recurrent gynecological cancer from are enrolled for this study. Eligible participants then provide fecal specimen, blood, vaginal swab, oral mucosal swab and receive food dietary recommendation. Additional samples are collected for results analysis.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

AdventHealth Cancer Institute

Orlando, Florida, 32804, United States

Location status: Recruiting

Location contact

James Kendrick, MD

SUB_INVESTIGATOR

Jessica Chestnut

CONTACT

[email protected]

407 303 2451

Nathalie McKenzie, MD

PRINCIPAL_INVESTIGATOR

Robert Holloway, MD

SUB_INVESTIGATOR

About this study

30 patients diagnosed with advanced or recurrent gynecological cancer who plan to receive immunotherapy treatment with a checkpoint inhibitor at AHMG AdventHealth Orlando Gynecological Oncology Group are recruited. Patients will be recruited 1-2 weeks prior to the beginning of treatment and appropriate informed consent will be obtained. Fecal samples; blood; saliva and vaginal swab samples will be collected among participants prior to their first treatment, after four doses of immunotherapy, and again at the completion of immunotherapy (follow-up). These 4 biomarker samples will undergo metatranscriptomic analysis, also known as RNAseq, method of sample analysis. Only RNA molecules are sequenced, while DNA is degraded. for bacterial community analysis. These findings will help to design a future study to examine the role of the gut microbiome in antitumor immunity and its effect on immune checkpoint inhibitor therapy for advanced or recurrent gynecological cancer. NHANES Food Frequency Questionnaire will be collected prior to participants' first treatments.

The short-term goals of this pilot study are to obtain preliminary data on the gut bacterial microbiome of patients with advanced or recurrent gynecological cancer. The long-term goals of this study is to begin to understand how the gut microbiome changes within an individual patient undergoing immunotherapy, to gut microbiome differs among patients undergoing immunotherapy, and to examine whether the gut microbiome is associated with the response to cancer immunotherapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult females > 18 years old
  • Advanced or recurrent gynecological cancer patients from AHMG Advent Health Orlando Gynecologic Oncology Group
  • Patients for whom an immunotherapy regimen has been ordered

Exclusion criteria

  • Patients unable to provide fecal specimens at three time points
  • Patients unable to read or understand informed consent
  • Taking medications that may affect gut microbiome:
  • Proton pump inhibitors (PPIs)
  • Metformin
  • Antibiotics
  • Laxatives
  • Patients who are receiving investigational agent

Treatment and study plan

Primary outcomes

  1. Microbiome change through analysis of biological samples (fecal specimen, blood, vaginal swab, oral mucosal swab).

    Time frame: ~2 years

    Changes are measured between the genetic microbiome signatures of advanced or recurrent gynecological cancer patients who are receiving immune checkpoint inhibitors.

Study contacts

Contact information is provided by the study sponsor or research team.

Momchilo Vuyisich, PhD

CONTACT

[email protected]

855 958 4663

Ryan Toma, MS

CONTACT

Sponsors and collaborators

Lead sponsor

Viome

Industry

Collaborators

  • AdventHealth

Registry information

Official study title

Pilot Feasibility Study of the Interplay Between the Host Gut Microbiome and Efficacy of Treatment for Advanced or Recurrent Gynecological Cancer Patients Receiving Immunotherapy

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Jul 12, 2021
Registry last updated
Jan 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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