Fludeoxyglucose F 18 PET Imaging in Determining Protein and Gene Expression Signatures in Patients With Premalignant Polyps or Colon Cancer
Status: | Completed |
---|---|
Conditions: | Colorectal Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 15 - Any |
Updated: | 4/21/2016 |
Start Date: | September 2007 |
End Date: | September 2011 |
Pilot Study of Ex-Vivo Molecular Polyp Imaging Using 18-F Fluorodeoxyglucose (FGD) Positron Emission Tomography (PET) in the Determination of Protein and Gene Expression Signatures of Premalignant Polyps
RATIONALE: Diagnostic imaging procedures, such as fludeoxyglucose F 18 PET, may be effective
in detecting cancer or recurrence of cancer, or premalignant polyps.
PURPOSE: This clinical trial is studying fludeoxyglucose F 18-PET imaging to see how well it
works in determining protein and gene expression signatures in patients with premalignant
polyps or colon cancer.
in detecting cancer or recurrence of cancer, or premalignant polyps.
PURPOSE: This clinical trial is studying fludeoxyglucose F 18-PET imaging to see how well it
works in determining protein and gene expression signatures in patients with premalignant
polyps or colon cancer.
OBJECTIVES:
Primary
- To determine the feasibility of ex-vivo imaging of colon cancer and colon polyps using
fludeoxyglucose F 18 positron emission tomography (FDG PET).
- To evaluate the differences in molecular and genetic profiles between FDG-positive
polyps and FDG-negative polyps to suggest what gene mutations and abnormal mRNA and/or
protein expressions may be required for FDG avidity ("signature" for FDG avidity).
Secondary
- To evaluate the differences in molecular and genetic profiles between FDG-positive
polyps and FDG-positive cancers to suggest what gene mutations and abnormal mRNA and/or
protein expressions may be required for cancer formation ("signature" for cancer).
- To evaluate the differences in molecular and genetic profiles between normal colonic
mucosa, polyps, and cancer.
- To evaluate the differences and similarities in molecular and genetic profiles between
FDG-positive cancers and polyps.
OUTLINE: Part I: Patients receive fludeoxyglucose F 18 (FDG) IV followed 45-60 minutes later
by surgery to remove part or all of the colon. Tissue samples of the colon undergo positron
emission tomography (PET) imaging.
Part II: Tissue samples are analyzed for glucose transporters proteins (Glut-1, 2, 3, 4, 5,
7) via IHC; presence of K-ras mutation (invariable mutant site on codon 12, 13) via PCR; 18q
deletion via fluorescence in situ hybridization (FISH) or DCC IHC; MCT-1, Hex-1, Hex-2, and
COX-2 expression levels via quantitative RT-PCR method or western blot; APC mutation via
PCR- In Vitro Synthesized-Protein Assay or RT-PCR direct sequencing method; p53 mutation
detection via immunochemistry, RT-PCR direct sequence methods, and western blot; methylation
alteration of MGMT, CDKN2A, HLTF, MLH1, TIMP3, HIF1, BNIP3, and HRK via methylation
detecting microchip; and specific gene methylations via methylation-specific PCR. Some
tissue samples may be saved and banked for future studies.
Primary
- To determine the feasibility of ex-vivo imaging of colon cancer and colon polyps using
fludeoxyglucose F 18 positron emission tomography (FDG PET).
- To evaluate the differences in molecular and genetic profiles between FDG-positive
polyps and FDG-negative polyps to suggest what gene mutations and abnormal mRNA and/or
protein expressions may be required for FDG avidity ("signature" for FDG avidity).
Secondary
- To evaluate the differences in molecular and genetic profiles between FDG-positive
polyps and FDG-positive cancers to suggest what gene mutations and abnormal mRNA and/or
protein expressions may be required for cancer formation ("signature" for cancer).
- To evaluate the differences in molecular and genetic profiles between normal colonic
mucosa, polyps, and cancer.
- To evaluate the differences and similarities in molecular and genetic profiles between
FDG-positive cancers and polyps.
OUTLINE: Part I: Patients receive fludeoxyglucose F 18 (FDG) IV followed 45-60 minutes later
by surgery to remove part or all of the colon. Tissue samples of the colon undergo positron
emission tomography (PET) imaging.
Part II: Tissue samples are analyzed for glucose transporters proteins (Glut-1, 2, 3, 4, 5,
7) via IHC; presence of K-ras mutation (invariable mutant site on codon 12, 13) via PCR; 18q
deletion via fluorescence in situ hybridization (FISH) or DCC IHC; MCT-1, Hex-1, Hex-2, and
COX-2 expression levels via quantitative RT-PCR method or western blot; APC mutation via
PCR- In Vitro Synthesized-Protein Assay or RT-PCR direct sequencing method; p53 mutation
detection via immunochemistry, RT-PCR direct sequence methods, and western blot; methylation
alteration of MGMT, CDKN2A, HLTF, MLH1, TIMP3, HIF1, BNIP3, and HRK via methylation
detecting microchip; and specific gene methylations via methylation-specific PCR. Some
tissue samples may be saved and banked for future studies.
Subject Inclusion Criteria:
- Patients eligible for entry into the study are those:
- Age 15 to 100
- Undergoing resection of a non-sarcomatous primary colon neoplasm who also has 2 or
more adenomas each greater than or equal to 7-10mm in size which are anticipated to
be removed with the colon specimen.
- It will be known from MSKCC or outside studies (barium enema, endoscopy, PET/CT, or
CT colonography) that the patient has at least 2 proven adenomas 7-10 mm or greater
and a primary colon neoplasm
Subject Exclusion Criteria:
- Insulin-dependent diabetics (as established by routine history and presurgical
laboratory tests).
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