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Clinical Trials/NCT01104129
NCT01104129
Completed
Not Applicable

Detection of Pancreatic Cancer and Pre-cancer by Stool DNA Testing: A Feasibility Study

Columbia University1 site in 1 country158 target enrollmentJuly 9, 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pancreatic Cancer
Sponsor
Columbia University
Enrollment
158
Locations
1
Primary Endpoint
Positive mutation rate in tumors/IPMN lesions vs. control
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to determine if pancreatic cancer/pre-cancer can be detected in early stages through the molecular analysis of stool samples. Investigators hypothesize that analysis of stool samples using digital melt curve (DMC) analysis, can be used as a sensitive and specific method to detect the common genetic abnormalities present in pancreatic cancers and pre-cancerous lesions of the pancreas.

Detailed Description

Pancreatic ductal adenocarcinoma (PDC) remains the fourth leading cause of cancer-related death in the United States. This is largely due to the fact that most patients present with advanced, unresectable disease, highlighting the critical need for a screening test for this disease. Stool testing is an approach that has not been explored for use in PDC screening. With the advent of stool-based DNA tests, it may be possible to target genetic abnormalities that have been recently characterized in PDC tumorigenesis. Aim: The aim of this study is to determine if deoxyribonucleic acid (DNA) alterations present in pancreatic cancer and precancerous intrapapillary mucinous neoplasms (IPMN) can be reliably recovered in matched stool. Methods: This is a case-control prospective study to determine the utility of a stool-based digital melt curve (DMC) assay in PDC screening. A total of 30 patients (18 with pancreatic cancer, 12 with IPMN) who will be undergoing pancreatic resection will be enrolled. Pancreatic neoplastic tissue will be isolated from their surgical specimens and the genes most commonly mutated in PDC will be sequenced from extracted DNA. In addition, hypermethylation at common promoter sites will be assessed by methylation-specific PCR. The genetic and epigenetic alterations isolated in pancreatic tissue will be utilized as the targets for stool DMC assay. Blinded technicians will process stool specimens from control patients as well as a matched control. The primary outcomes of this study will be the sensitivity and specificity of the stool DMC assay in detecting genetic mutations present in tumor or IPMN lesions.

Registry
clinicaltrials.gov
Start Date
July 9, 2009
End Date
November 29, 2016
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years of age and older.
  • Tissue-confirmed or radiological evidence of either pancreatic adenocarcinoma or intrapapillary mucinous neoplasm(IPMN).
  • Scheduled for surgical resection of the adenocarcinoma or IPMN.
  • Able to give informed consent

Exclusion Criteria

  • History of colorectal, gastric cancer, esophageal, or head-and-neck cancer.
  • Endoscopic procedure conducted less than 1 week prior to enrollment.
  • Unwillingness or inability to sign informed consent.

Outcomes

Primary Outcomes

Positive mutation rate in tumors/IPMN lesions vs. control

Time Frame: 30 days

The positive mutation rates in tumor or IPMN lesions and in matched controls will be assessed.

Secondary Outcomes

  • Percentage of patients with genetic abnormalities correctly detected in stool samples(30 days)

Study Sites (1)

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