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Feasibility Study Using Imaging Biomarkers in Lung Cancer

Primary Purpose

Lung Cancer

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Imaging Biomarkers
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Lung Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Subjects of all races and ethnic origins over 18 years of age will be recruited.
  • Patients must have suspicious or known to be malignant solitary pulmonary nodule,5cm or less in size.

Exclusion Criteria:

  • Patients with a contraindication to MRI examinations will be excluded from this study.

Contraindications to MRI examinations include:

  • Medically unstable

    • Heart failure
    • Unstable angina
    • Child bearing
    • Lactating
  • Not a surgical candidate
  • Any contraindication per MRI Screening Form (Appendix A attached). This is the same form used in clinical practice at UT Southwestern.

    • Titanium implants, pacemakers
    • Poorly controlled diabetes
    • Body weight greater than 300 pounds
    • Claustrophobic
  • Since each patient is receiving a gadolinium based contrast agent intravenously:

    • eGFR < 45 mL/min/1.73m2
    • Sickle cell disease
    • Hemolytic anemia

Sites / Locations

  • University of Texas Southwestern Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Surgery

Arm Description

The 13C-glucose solution will be given intravenously. It will be started at about the same time as the start of surgery, according to the study guidelines. The 13C-glucose IV solution will be stopped once the surgeon has removed the tumor tissue.

Outcomes

Primary Outcome Measures

DCE-MRI
Physicians and researchers will review the results of the imaging to determine if the patient will receive the [U-13C] glucose infusion.

Secondary Outcome Measures

C-13 isotopomer
Employ C-13 isotopomer analysis and metabolomics on specimens obtained from resected tissue of suitable patients in this cohort to determine the metabolic alterations present in lung cancer.

Full Information

First Posted
April 17, 2013
Last Updated
January 6, 2023
Sponsor
University of Texas Southwestern Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02095808
Brief Title
Feasibility Study Using Imaging Biomarkers in Lung Cancer
Official Title
Feasibility Study Using Imaging Biomarkers in Lung Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 20, 2013 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research study is to develop a method of using magnetic resonance imaging (MRI) to evaluate solitary pulmonary nodules (mass in the lung smaller than 3 centimeters). A pulmonary nodule is a mass or growth on the lung. An MRI is a scanning device that uses magnets to make images (pictures) of the body. This study is being done to determine what series of reactions (metabolic pathways) pulmonary nodules use as they burn sugar as fuel for growth. The manner in which the tumor burns (metabolizes) sugar for fuel is being investigated by using a natural, slightly modified, sugar solution (13C-glucose) and studying a small sample of the tumor once it is removed at the time of surgery.
Detailed Description
The recent report of the findings of the National Lung Screening Trial indicates that screening a high-risk population using low dose CT results in a 20% reduction in lung cancer mortality. At our institution, some of positive nodules that are 1 cm or larger would be imaged using combined fluoro-deoxyglucose positron emission tomography (FDG PET)/CT. Highly suspicious nodules would be biopsied if the risks were manageable. Otherwise, the suspicious nodules not eligible for biopsy and so-called "indeterminate" nodules are followed using CT to be evaluated for interval growth. The overall goal of this project is to assess several very promising imaging biomarkers that can reflect either the physiological or metabolic status of these nodules in order to develop more accurate imaging algorithms for follow-up that are either less invasive or do not use ionizing radiation or both. Based on our experience with other cancers and our preliminary results in lung cancer, we have identified four potential imaging studies that we believe have the potential to result in validated "imaging biomarkers" that can either individually, or in combination, characterize malignancies. Since tumors tend to exhibit angiogenesis and altered vascular permeability, we and others, have found that analyses of dynamic contrast enhanced MRI (DCEMRI) can be employed as "imaging biomarkers" for malignancy. Tumors often exhibit higher cellularity than benign or normal tissue suggesting that pixel-by-pixel ADC values derived from diffusion weighted MRI could be useful imaging biomarkers. Finally, measuring alterations in metabolic fluxes through the use of pathway specific C-13 labeled compounds, a technique pioneered here at the Advanced Imaging Research Center (AIRC) at UT Southwestern, has shown the capability of providing metabolic fingerprints for malignant and benign tissue. This approach, while invasive, could identify and validate markers that can be detected non-invasively in future studies. We will also employ advanced metabolomics methods to identify potential signature "onco-metabolites" in these lung cancers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer

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
225 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Surgery
Arm Type
Experimental
Arm Description
The 13C-glucose solution will be given intravenously. It will be started at about the same time as the start of surgery, according to the study guidelines. The 13C-glucose IV solution will be stopped once the surgeon has removed the tumor tissue.
Intervention Type
Procedure
Intervention Name(s)
Imaging Biomarkers
Intervention Description
Want to see if using 13C-glucose helps in detecting cancer and deciding on a treatment plan.
Primary Outcome Measure Information:
Title
DCE-MRI
Description
Physicians and researchers will review the results of the imaging to determine if the patient will receive the [U-13C] glucose infusion.
Time Frame
One time - within 5 days of the scheduled surgery
Secondary Outcome Measure Information:
Title
C-13 isotopomer
Description
Employ C-13 isotopomer analysis and metabolomics on specimens obtained from resected tissue of suitable patients in this cohort to determine the metabolic alterations present in lung cancer.
Time Frame
During the infusion period blood samples will be collected every 30 minutes (for 2-3 hours) until the end of tumor sampling for mass spec and NMR analyisis of C-glucose in the blood.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects of all races and ethnic origins over 18 years of age will be recruited. Patients must have suspicious or known to be malignant solitary pulmonary nodule,5cm or less in size. Exclusion Criteria: Patients with a contraindication to MRI examinations will be excluded from this study. Contraindications to MRI examinations include: Medically unstable Heart failure Unstable angina Child bearing Lactating Not a surgical candidate Any contraindication per MRI Screening Form (Appendix A attached). This is the same form used in clinical practice at UT Southwestern. Titanium implants, pacemakers Poorly controlled diabetes Body weight greater than 300 pounds Claustrophobic Since each patient is receiving a gadolinium based contrast agent intravenously: eGFR < 45 mL/min/1.73m2 Sickle cell disease Hemolytic anemia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jeffery Wilson
Phone
214-648-7097
Email
Jeffery.Wilson@utsouthwestern.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kemp H Kernstine, MD
Organizational Affiliation
University of Texas Southwestern Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas Southwestern Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeffery Wilson
Phone
214-648-7097
Email
Jeffery.Wilson@utsouthwestern.edu

12. IPD Sharing Statement

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Feasibility Study Using Imaging Biomarkers in Lung Cancer

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