Official Title: “Development of the Pancreatic Cancer Collaborative Registry and Risk Assessment Models; 2) Biomedical Computing Tools for Pancreatic Cancer Research; 3) Pancreatic Cancer Pre-Validation Reference Set for Serum/Plasma Biomarkers; 4) Semantically Integrative Pancreatic Cancer Registry (SRC)”

RATIONALE: Gathering information about patients with cancer may help doctors learn more about the disease and plan early diagnosis and treatment.

PURPOSE: This clinical trial is studying computer tools for improving early diagnosis and treatment in patients with pancreatic cancer, are at risk for pancreatic cancer, or have a non-cancerous pancreatic disorder.

Study Type: Observational

Study Design: N/A

Study Primary Completion Date: December 2012

OBJECTIVES: - Develop Integrated Biomedical Computing Tools (IBCT) for the better understanding and treatment of pancreatic cancer by using the power of computer and informatics sciences. - Continue development of the Pancreatic Cancer Collaborative Registry (PCCR) infrastructure to act as a repository for socio-demographic, environmental, clinical, and family history data collected from individuals and interested family members with a personal and/or family history of pancreatic cancer. - Participate in an international pancreatic registry known as the PCCR by sharing information collected for research purposes only, to be used by pancreatic cancer research collaborators from other institutions. - Collect and bank excess biological materials (i.e., pancreatic tissue, tumor tissue, and/or metastatic pancreatic cancer tissue, and/or paraffin-embedded tissue), blood, and serum from registry participants for future research. - Establish an infrastructure with core data elements and standardized operating procedures for specimen collection, processing, and storage for the EDRN Pancreatic Cancer Working Group project to use as a resource for the development of biomarkers for the early detection of pancreatic adenocarcinoma.

OUTLINE: This is a multicenter study.

Patients undergo blood and pancreatic tissue collection. Normal, tumor, and/or metastatic pancreatic cancer tissue, and/or paraffin-embedded tissue from prior surgery or biopsy are obtained.

Patients provide or complete personal information about themselves, their medical history, their diet and lifestyle habits, any past or current environmental exposures, and re-create their family tree for any cancers that have occurred in any of their family members. Clinical data is collected annually.

Control participants provide blood samples and complete questionnaires at baseline. Clinical data is collected annually.

PROJECTED ACCRUAL: A total of 60 patients per group (i.e., cancer cases, healthy controls, acute biliary obstruction cases, and chronic pancreatitis cases) for a total of 240 patients will be accrued for this study.

Intervention(s) in this Clinical Trial

• Procedure: biopsy
• Procedure: medical chart review
• Procedure: questionnaire administration
• Procedure: study of socioeconomic and demographic variables

Primary Measures

• Development of integrated Biomedical Computing Tools
  • Safety Issue?: No
• Development of the Pancreatic Cancer Collaborative Registry (PCCR) infrastructure as a repository for socio-demographic, environmental, clinical, and family history data
  • Safety Issue?: No
• Participation in the international pancreatic registry known as the PCCR by sharing information
  • Safety Issue?: No
• Collection and banking of excess biological materials (i.e., pancreatic tissue, tumor tissue ,and/or metastatic pancreatic cancer tissue, and/or paraffin-embedded tissue), blood, and serum
  • Safety Issue?: No
• Establishment of an infrastructure with core data elements and standardized operating procedures for specimen collection, processing, and storage
  • Safety Issue?: No

DISEASE CHARACTERISTICS:

• Patients must meet 1 of the following criteria:
• Histologically confirmed adenocarcinoma of the pancreas
• Resectable stage I-IIA disease or stage IIB or higher disease
• Must have undergone complete surgical resection of the tumor with curative intent
• Pancreatic mass (solid) that is less than 4 cm as determined by any conventional imaging (MRI, EUS, or CT scan)
• No evidence of extension of the mass beyond the pancreas including vascular invasion or invasion into surrounding organs, with the exception of the bile duct
• No imaging evidence of metastatic disease or lymphadenopathy (lymph nodes greater than 1 cm and/or appearance suspicious for an advanced lesion by imaging criteria)
• Has a family history of pancreatic cancer and is considered to be an at-risk individual for the disease (i.e., member of a family with 2 or more individuals with pancreatic cancer)
• Control participants must meet 1 of the following criteria:
• Chronic pancreatitis OR history of exocrine insufficiency meeting the following criteria:
• At least 2 of the following criteria are met (unless patient has a history of pancreatic exocrine insufficiency in which case only 1 criterion must be met):
• Abdominal ultrasound that is consistent with chronic pancreatitis by standard radiological criteria (i.e., echogenic foci in the parenchyma, large or small cavities, calcifications, or dilated pancreatic duct)
• Abdominal CT scan consistent with chronic pancreatitis by standard radiological criteria (i.e., calcifications, dilated pancreatic duct, irregular contour of the gland, or cystic lesions)
• Endoscopic retrograde cholangiopancreatography exam consistent with chronic pancreatitis by standard radiological criteria (i.e., dilated tortuous main pancreatic duct with irregular secondary branches or intraductal calculi)
• Endoscopic ultrasound consistent with chronic pancreatitis by standard radiological criteria (i.e., echogenic foci, focal regions of decreased echogenicity, or pancreatic ductal changes)
• Pancreatic calcifications identified on plain film of the abdomen
• Must have an imaging study of the pancreas within 3 months of study enrollment that does not suggest a pancreatic mass
• Stable clinical history over the past year with no suspicion for cancer due to weight loss, jaundice, or change in abdominal symptoms
• No family history of pancreatic cancer
• Acute biliary obstruction (stones) including jaundice of benign etiology meeting the following criteria:
• Elevation of serum bilirubin level greater than 2.0 mg/dL
• Dilated extrahepatic biliary systems demonstrated on US, MRI, or CT scan
• Blood sample available within 72 hours of admission and prior to any corrective intervention
• Biliary obstruction must be of benign etiology such as common bile duct stone or benign biliary stricture
• Must have complete imaging study performed of the pancreas that does not suggest a pancreatic cancer (i.e., discrete mass lesion)
• No family history of pancreatic cancer
• Healthy control meeting the following criteria:
• Age, race, and sex-matched to qualified pancreatic cancer cases
• No family history of pancreatic cancer
• No personal history of acute pancreatitis or biliary obstruction (stones) including jaundice of benign etiology
• No concurrent abdominal pain
• No concurrent unexplained weight loss

PATIENT CHARACTERISTICS:

• No prior malignancy, except nonmelanoma skin cancer, for 10 years

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• No prior preoperative chemoradiotherapy (neoadjuvant)

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: N/A

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Sponsor: University of Nebraska

Overall Clinical Trial Officials and Contacts

Simon Sherman, PhD Principal Investigator University of Nebraska  

Information obtained from ClinicalTrials.gov on October 10, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00661882

Study ID Number: CDR0000582361

ClinicalTrials.gov Identifier: NCT00661882

Health Authority: Unspecified

Clinical trial summary from the National Cancer Institute's PDQ® database