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A Pilot Study to Determine Fructose Uptake by Primary Human Colorectal Tumors

Primary Purpose

Colorectal Tumors

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cohort 1: HFCS (fructose) fed
Cohort 2: D-Xylose (xylose-fed)
Sponsored by
Weill Medical College of Cornell University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Colorectal Tumors focused on measuring Fructose, D-Xylose, Primary Human Colorectal Tumors

Eligibility Criteria

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

Inclusion Criteria:

  • Subjects of 18 years of age or older, male, and female
  • Subjects with a diagnosis of invasive non-hereditary colonic adenocarcinoma who will be undergoing standard of care (SOC) laparoscopic, robot-assisted, or open surgical resection
  • The subject provides informed consent

Exclusion Criteria:

  • Subjects with a history of uncontrolled diabetes mellitus (A1C >7.0) Type I and Type 2, will be excluded to avoid potential confounders associated with the consumption of a large bolus of sugar (e.g., hyperglycemia and hyperinsulinemia)
  • Inflammatory Bowel Disease (Ulcerative Colitis or Crohn's Disease)
  • Patients on steroid medications
  • Patients with current infectious disease
  • Subjects who do not speak English

Sites / Locations

  • Weill Cornell MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Cohort 1: HFCS (fructose-fed)

Cohort 2: D-Xylose (xylose-fed)

Arm Description

Day Before Surgery between 09:00 pm and 10:00 pm Subjects will prepare the sugar solutions (Fructose-containing solution: 250 mL of water containing 41.25 g of D-Fructose and 33.75 g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Subjects will be reminded the day before the surgery to drink the solution.

Day Before Surgery between 09:00 pm and 10:00 pm Subjects will prepare the sugar solutions (Xylose-containing solution: 250 mL of water containing 41.25 g of D-Xylose and 33.75g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Subjects will be reminded the day before the surgery to drink the solution.

Outcomes

Primary Outcome Measures

The abundance of fructose in tumor extracts
The abundance of fructose in tumor extracts assessed by mass spectrometry in the morning after the consumption of oral sugar solutions.

Secondary Outcome Measures

The abundance of Fructose and [13C]-Fructose in the blood
The abundance of Fructose and [13C]-Fructose in the blood in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Abundance of Fructose and [13C]-Fructose in the urine
The abundance of Fructose and [13C]-Fructose in the urine in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Abundance of Fructose and [13C]-Fructose in the liver
The abundance of Fructose and [13C]-Fructose in the liver tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Abundance of Fructose and [13C]-Fructose in the intestine
The abundance of Fructose and [13C]-Fructose in the intestine tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Abundance of Fructose and [13C]-Fructose in the mesentery tissues
The abundance of Fructose and [13C]-Fructose in the mesentery tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
The abundance of Xylose and [13C]-Xylose in the blood
The abundance of Xylose and [13C]-Xylose in the blood in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
The abundance of Xylose and [13C]-Xylose in the urine
The abundance of Xylose and [13C]-Xylose in the urine in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
The abundance of Xylose and [13C]-Xylose in the liver
The abundance of Xylose and [13C]-Xylose in the liver tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
The abundance of Xylose and [13C]-Xylose in the intestinal tissue
The abundance of Xylose and [13C]-Xylose in the intestinal tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
The abundance of Xylose and [13C]-Xylose in the mesentery tissues
The abundance of Xylose and [13C]-Xylose in the mesentery tissues in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
The abundance of Xylose and [13C]-Xylose in the in the tumor
The abundance of Xylose and [13C]-Xylose in the tumor in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.

Full Information

First Posted
November 11, 2021
Last Updated
February 22, 2023
Sponsor
Weill Medical College of Cornell University
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1. Study Identification

Unique Protocol Identification Number
NCT05136092
Brief Title
A Pilot Study to Determine Fructose Uptake by Primary Human Colorectal Tumors
Official Title
A Pilot Study to Determine Fructose Uptake by Primary Human Colorectal Tumors
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 16, 2022 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Weill Medical College of Cornell University

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
This proposed study is designed to investigate the specific uptake of fructose by human colorectal tumors. In this study, subjects with colorectal cancer undergoing surgery will receive an oral sugar solution containing fructose or xylose prior to surgery. The tumor will then be resected, and a portion of the tissue will be used to measure the abundance of fructose and xylose. The study hypothesis is that the tumors will take up fructose sugar but not xylose sugar. A comparison of the sugar uptake between the tumor and normal tissues from the adjacent intestinal epithelium and smooth muscle and the liver will be conducted. This proposal will confirm that human colorectal cancer tumors can directly absorb dietary sugars, which has never been demonstrated.
Detailed Description
This prospective pilot study is designed to investigate the uptake of dietary fructose and xylose by primary human colon tumors. In this study, the recruited patients with colorectal cancer will receive an oral sugar solution containing either Fructose sugar or Xylose sugar before surgery. The tumor will then be resected and a portion of the tumor, normal intestinal tissue, blood, urine, and liver will be used to quantify fructose and xylose. Research question Can primary human tumors take up fructose or xylose? A statement of the hypothesis The hypothesis is that fructose, but not xylose, can be directly absorbed and stored by primary human colon tumors. Design Prospective, non-randomized, pilot, feasibility, single-center, open-label, phase 1, investigator-initiated study to evaluate the uptake of dietary fructose and xylose by primary human colon tumors with 12 subjects in 2 cohorts: Cohort 1: 6 subjects will consume a sugar solution containing fructose and Cohort 2: 6 subjects will consume a sugar solution containing xylose. Eligible subjects that are scheduled to undergo colorectal resection for cancer treatment will be invited to participate in the study in consecutive order from the practice of colorectal surgeons at the time of their preoperative clinic visit. First, Cohort 1 subjects will be enrolled followed by the Cohort 2 subjects. N=12 Subjects Cohort 1: Fructose sugar solution =6 Subjects Cohort 2: Xylose sugar solution=6 Subjects

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Tumors
Keywords
Fructose, D-Xylose, Primary Human Colorectal Tumors

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Prospective, pilot, feasibility, single-center, non-randomized, open-label, phase 1, investigator-initiated study to evaluate the specific uptake of fructose by human colorectal tumors with 12 subjects in 2 cohorts: Cohort 1: fructose-fed with 6 subjects Cohort 2: xylose-fed with 6 subjects. Eligible subjects scheduled to undergo colorectal resection for cancer treatment will be invited to participate in the study in consecutive order from the practice of colorectal surgeons at the time of their preoperative clinic visit. First, Cohort 1 subjects will be enrolled followed by the Cohort 2 subjects.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cohort 1: HFCS (fructose-fed)
Arm Type
Experimental
Arm Description
Day Before Surgery between 09:00 pm and 10:00 pm Subjects will prepare the sugar solutions (Fructose-containing solution: 250 mL of water containing 41.25 g of D-Fructose and 33.75 g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Subjects will be reminded the day before the surgery to drink the solution.
Arm Title
Cohort 2: D-Xylose (xylose-fed)
Arm Type
Experimental
Arm Description
Day Before Surgery between 09:00 pm and 10:00 pm Subjects will prepare the sugar solutions (Xylose-containing solution: 250 mL of water containing 41.25 g of D-Xylose and 33.75g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Subjects will be reminded the day before the surgery to drink the solution.
Intervention Type
Dietary Supplement
Intervention Name(s)
Cohort 1: HFCS (fructose) fed
Intervention Description
Day Before Surgery Subjects will prepare the sugar solutions (Fructose-containing solution: 250 mL of water containing 41.25 g of D-Fructose and 33.75 g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Samples collected before surgery: Blood sample of 5 ml Urine Samples 5 ml Day of Surgery The anesthesia and surgical procedure will undergo as per regular care. Samples collection at the time the surgical specimen is removed Blood sample of 5 ml blood will be obtained from the IV line Tissue samples 2 Tumor tissue samples 5mmx5mmx5mm, 2 Intestinal /colon tissue samples 5mmx5mmx5mm 2 tissue samples from mesentery tissue 5mmx5mmx5mm Liver Biopsy - a 3-5 mm liver tissue will be obtained for research. Urine Samples 5 ml
Intervention Type
Dietary Supplement
Intervention Name(s)
Cohort 2: D-Xylose (xylose-fed)
Intervention Description
Day Before Surgery Subjects will prepare the sugar solutions (Xylose-containing solution: 250 mL of water containing 41.25 g of D-Xylose and 33.75g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Samples collected before surgery: Blood sample of 5 ml Urine Samples 5 ml Day of Surgery The anesthesia and surgical procedure will undergo as per regular care. Samples collection at the time the surgical specimen is removed Blood sample of 5 ml blood will be obtained from the IV line Tissue samples 2 Tumor tissue samples 5mmx5mmx5mm, 2 Intestinal /colon tissue samples 5mmx5mmx5mm 2 tissue samples from mesentery tissue 5mmx5mmx5mm Liver Biopsy - a 3-5 mm liver tissue will be obtained for research. Urine Samples 5 ml
Primary Outcome Measure Information:
Title
The abundance of fructose in tumor extracts
Description
The abundance of fructose in tumor extracts assessed by mass spectrometry in the morning after the consumption of oral sugar solutions.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Secondary Outcome Measure Information:
Title
The abundance of Fructose and [13C]-Fructose in the blood
Description
The abundance of Fructose and [13C]-Fructose in the blood in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
Abundance of Fructose and [13C]-Fructose in the urine
Description
The abundance of Fructose and [13C]-Fructose in the urine in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
Abundance of Fructose and [13C]-Fructose in the liver
Description
The abundance of Fructose and [13C]-Fructose in the liver tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
Abundance of Fructose and [13C]-Fructose in the intestine
Description
The abundance of Fructose and [13C]-Fructose in the intestine tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
Abundance of Fructose and [13C]-Fructose in the mesentery tissues
Description
The abundance of Fructose and [13C]-Fructose in the mesentery tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
The abundance of Xylose and [13C]-Xylose in the blood
Description
The abundance of Xylose and [13C]-Xylose in the blood in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
The abundance of Xylose and [13C]-Xylose in the urine
Description
The abundance of Xylose and [13C]-Xylose in the urine in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
The abundance of Xylose and [13C]-Xylose in the liver
Description
The abundance of Xylose and [13C]-Xylose in the liver tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
The abundance of Xylose and [13C]-Xylose in the intestinal tissue
Description
The abundance of Xylose and [13C]-Xylose in the intestinal tissue in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
The abundance of Xylose and [13C]-Xylose in the mesentery tissues
Description
The abundance of Xylose and [13C]-Xylose in the mesentery tissues in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)
Title
The abundance of Xylose and [13C]-Xylose in the in the tumor
Description
The abundance of Xylose and [13C]-Xylose in the tumor in the morning after the consumption of oral sugar solutions assessed by mass spectrometry.
Time Frame
Morning after the consumption of oral sugar solutions(during surgery at the time of specimen removal)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects of 18 years of age or older, male, and female Subjects with a diagnosis of invasive non-hereditary colonic adenocarcinoma who will be undergoing standard of care (SOC) laparoscopic, robot-assisted, or open surgical resection The subject provides informed consent Exclusion Criteria: Subjects with a history of uncontrolled diabetes mellitus (A1C >7.0) Type I and Type 2, will be excluded to avoid potential confounders associated with the consumption of a large bolus of sugar (e.g., hyperglycemia and hyperinsulinemia) Inflammatory Bowel Disease (Ulcerative Colitis or Crohn's Disease) Patients on steroid medications Patients with current infectious disease Subjects who do not speak English
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jujhar Singh
Phone
646-962-2789
Email
jus4018@med.cornell.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Julianna Brouwer, MPH
Phone
6469622789
Email
jub2024@med.cornell.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alessio Pigazzi, MD,PhD
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Weill Cornell Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jujhar Singh
Phone
646-962-2789
Email
jus4018@med.cornell.edu
First Name & Middle Initial & Last Name & Degree
Julianna Brouwer, MPH
Phone
646 -962-2789
Email
jub2024@med.cornell.edu
First Name & Middle Initial & Last Name & Degree
Alessio Pigazzi, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Pilot Study to Determine Fructose Uptake by Primary Human Colorectal Tumors

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