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Microbiome and Rectal Cancer

Primary Purpose

Rectal Cancer, Locally Advanced Malignant Neoplasm

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tissue collection
Sponsored by
University of South Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Rectal Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years old
  • Locally Advanced Rectal Adenocarcinoma (T3)
  • Standard 5FU based chemoradiation
  • Total Neoadjuvant Therapy per OPRA protocol guidelines

Exclusion Criteria:

  • Age < 18 years
  • Stage I or Stage IV rectal adenocarcinoma
  • Rectal cancer other than adenocarcinoma
  • Genetically associated cancer (HNPCC, FAP etc.) or highly suspicious for genetically associated cancer
  • Prior history of rectal adenocarcinoma (i.e. recurrent colorectal adenocarcinoma)

Sites / Locations

  • Tampa General Hospital
  • University of South Florida - South Tampa Campus
  • University of South Florida

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Tissue collection

Arm Description

Tissue collection

Outcomes

Primary Outcome Measures

16s rRNA gene sequencing to study bacterial phylogeny and taxonomy
16s rRNA sequencing from biopsy specimens

Secondary Outcome Measures

rectal microbiota to study bacteria strains
rectal microbiota - bacteria strains from biopsy specimens

Full Information

First Posted
November 12, 2019
Last Updated
July 31, 2023
Sponsor
University of South Florida
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1. Study Identification

Unique Protocol Identification Number
NCT04223102
Brief Title
Microbiome and Rectal Cancer
Official Title
Rectal Microbiome Variability Among Rectal Cancer Cohorts Including Complete Clinical Responders, Pathologic Responders, and Early Recurrence
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 18, 2020 (Actual)
Primary Completion Date
January 2027 (Anticipated)
Study Completion Date
June 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of South Florida

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of our study is to determine if an association exists between the microbiome of those with rectal adenocarcinoma who are complete pathologic responders and those who have a partial or no response to neoadjuvant therapy.
Detailed Description
This study will help to further elucidate the association of bacteria with rectal cancer, while also characterizing the genes associated with that risk. Furthermore it will attempt to better understand which patients may have an optimal response to neoadjuvant chemoradiation allowing for possible predictive metagenomics evaluation, investigators may be able to augment treatments as well as provide recommendations for the success and cost effectiveness of cancer care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer, Locally Advanced Malignant Neoplasm

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tissue collection
Arm Type
Other
Arm Description
Tissue collection
Intervention Type
Procedure
Intervention Name(s)
Tissue collection
Intervention Description
A flexible sigmoidoscopy is a procedure in which a flexible tubularized camera approximately 1 cm in diameter is inserted into the anus and advanced proximally to the sigmoid colon (approximately 20 cm). At that time a rectal biopsy of the tumor will be obtained as well as a sample from >5cm proximal to the tumor, with a separate biopsy forcep. Tattoo injection, as standard of care, will be performed within 1 cm distal to the tumor to identify the location in the future or for surgical intervention. If there is inability to get proximal to the tumor then a location at least 5 cm adjacent in any direction will be sufficient so long as it is grossly normal appearing.
Primary Outcome Measure Information:
Title
16s rRNA gene sequencing to study bacterial phylogeny and taxonomy
Description
16s rRNA sequencing from biopsy specimens
Time Frame
5 years
Secondary Outcome Measure Information:
Title
rectal microbiota to study bacteria strains
Description
rectal microbiota - bacteria strains from biopsy specimens
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years old Locally Advanced Rectal Adenocarcinoma (T3) Standard 5FU based chemoradiation Total Neoadjuvant Therapy per OPRA protocol guidelines Exclusion Criteria: Age < 18 years Stage I or Stage IV rectal adenocarcinoma Rectal cancer other than adenocarcinoma Genetically associated cancer (HNPCC, FAP etc.) or highly suspicious for genetically associated cancer Prior history of rectal adenocarcinoma (i.e. recurrent colorectal adenocarcinoma)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James R Williams, MD
Organizational Affiliation
University of South Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tampa General Hospital
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
Facility Name
University of South Florida - South Tampa Campus
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
Facility Name
University of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Microbiome and Rectal Cancer

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