Screening for Early Pancreatic Neoplasia (Cancer of the Pancreas Screening or CAPS4 Study)
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Purpose
CAPS4 is a study at Johns Hopkins Hospital to study the diagnosis and long-term outcomes of screening patients with an increased inherited risk for pancreatic cancer.
| Condition |
|---|
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Early Pancreatic Neoplasia Familial Pancreatic Neoplasia |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Screening for Early Pancreatic Neoplasia (Cancer of the Pancreas Screening or CAPS4 Study) |
- This clinical study will assess the diagnostic yield of a clinical screening program for early pancreatic neoplasia in high risk individuals. [ Time Frame: 5 years ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples With DNA
blood, pancreatic juices
| Estimated Enrollment: | 900 |
| Study Start Date: | June 2008 |
| Estimated Study Completion Date: | July 2016 |
| Estimated Primary Completion Date: | July 2016 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
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High Risk Group 1
familial Peutz-Jeghers syndrome
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High Risk Group 2
familial pancreatic cancer relatives
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High Risk Group 3
germline mutation carriers BRCA1, BRCA2, PRSS, PALB2, p16
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High Risk Group 4
young-onset pancreatic cancer relative
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High Risk Group 5
both parents affected
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Control 1
negative controls
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Control 2
chronic pancreatitis
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Control 3
pancreatic cancer
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Control 4
intraductal papillary mucinous neoplasm (IPMN)
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Detailed Description:
Pancreatic cancer is a deadly disease and the only hope for improvement of survival is early detection. Certain genetic syndromes are associated with a high risk of pancreatic cancer and screening for pancreatic cancer has become a relatively new strategy for familial pancreatic cancer. . Our pancreatic cancer research group at Johns Hopkins and others have shown that screening with EUS and/or abdominal imaging tests such as CT/MRI can detect a relatively high number of significant pancreatic neoplasms (7-18%) in asymptomatic high risk individuals with an inherited predisposition for pancreatic ductal adenocarcinoma This is a clinical, early detection translational study that will directly influence patient care. This long term study follows the successful completion of single center Cancer of the Pancreas (CAPS) 1 and CAPS 2 studies at Johns Hopkins, and the ongoing CAPS 3 multicenter study. GENERAL AIM: This is a study that aims to evaluate the diagnostic yield, quality of life, and clinical outcomes of a clinical screening and surveillance program for individuals at-risk for pancreatic cancer and to validate a candidate panel of biomarkers for early detection of pancreatic neoplasia. The 3 specific groups to be screened and followed are individuals from familial pancreatic cancer kindreds (who have 2 or more affected relatives and have an estimated risk 16-57 times that of controls), patients with familial Peutz-Jeghers syndrome, patients with a known BRCA-2, BRCA-1, PALB2, PRSS or p16 germline mutation.
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
asymptomatic high risk patients
Inclusion Criteria:
High Risk Group 1 (familial Peutz-Jeghers syndrome):
- At least 30 years old and < 80 years old, and
- at least 2 of 3 criteria diagnostic of Peutz-Jeghers syndrome (characteristic intestinal hamartomatous polyps, mucocutaneous melanin deposition, or family history of Peutz-Jeghers syndrome)
- known STK-11 gene mutation carrier
High Risk Group 2 (familial pancreatic cancer relatives):
- > 50 years old or 10 years younger than the age of youngest relative with pancreatic cancer, and < 80 years old
- come from a family with 2 or more members with a history of pancreatic cancer (2 of which have a first-degree relationship consistent with familial pancreatic cancer), and
- have a first-degree relationship with at least one of the relatives with pancreatic cancer.
If there are 2 or more affected blood relatives, at least 1 must be a first-degree relative of the individual being screened
High Risk Group 3 (germline mutation carriers):
- > 40 years old or 10 years younger than the age of the youngest relative with pancreatic cancer, and< 80 years old
- patient is carrier of a known BRCA1, BRCA2, PALB2, or FAMMM (p16/CDKN2A) mutation, and there is > 1 pancreatic cancer in the family, one of whom is a first- or second-degree relative of the subject to be screened.
- Hereditary pancreatitis syndrome
High Risk Group 4 (young-onset pancreatic cancer relative):
- > 50 years old or 10 years younger than the age of youngest relative with pancreatic cancer, and < 80 years old
- have a first-degree relationship with at least one relative with young-onset pancreatic cancer ( age of onset < 50 years)
High risk group 5(both parents affected)
- > 50 years old or 10 years younger than the age of the youngest relative with pancreatic cancer, and< 80 years old
- two parents affected by pancreatic cancer
Control 1 (Negative Controls):
- are undergoing EUS and/or ERCP for non-pancreatic indications as part of their standard medical care, and
- have no clinical or radiologic suspicion of pancreatic disease (chronic pancreatitis or pancreatic cancer)
Control 2 (Chronic Pancreatitis)
- are undergoing EUS and/or ERCP for evaluation and/or treatment of suspected or proven chronic pancreatitis as part of their standard medical care, and,
- have no clinical or radiologic suspicion of pancreatic cancer
Control 3 (Pancreatic Cancer)
a. are undergoing EUS and/or ERCP for evaluation and/or treatment of suspected or proven pancreatic ductal adenocarcinoma (based on clinical and radiologic evidence)
- Control 4 (Intraductal Papillary Mucinous Neoplasm or IPMN) a. are undergoing EUS and/or ERCP for evaluation and/or treatment of suspected or proven pancreatic cancer precursor, intraductal papillary mucinous neoplasm (based on clinical presentation and radiologic or prior EUS or radiologic evidence of a dilated main pancreatic duct and/or pancreatic cystic lesion communicating with the pancreatic ductal system)
Additional requirements for eligible high risk patients: i) All persons with known genetic mutation must have proof of mutation status. Those who had research-related genetic testing must have confirmation by a clinical CLIA-certified laboratory. ii) A good faith attempt should be made to confirm pancreatic cancers in the family members via registration in a pancreatic cancer registry iii) The affected first degree relative of the person being screened must be confirmed by medical record or death certificate.
All control patients must be > 18 and < 80 years old and no personal or family history of pancreatic cancer or a germline mutation linked to pancreatic cancer.
Exclusion Criteria:
Patients will be excluded if they have any of the following:
- medical comorbidities or coagulopathy that contraindicate endoscopy,
- Karnosfky performance status of < 60,
- had partial or complete resection of their pancreas
- had a partial or complete gastrectomy with Billroth or Roux-en-Y anastomosis
- a stricture or obstruction in the upper GI tract that does not allow passage of the echoendoscope
- life expectancy less than 5 years due to coexisting advanced cancer or AIDS.
- inability to provide informed consent
- pregnant patient
- history of pancreatic cancer,
- suspicion of pancreatic neoplasia based on clinical history (weight loss, unexplained abdominal pain), physical examination (obstructive jaundice, cachexia), laboratory tests (cholestastic liver function tests, markedly elevated CA19-9), and/or imaging studies (pancreatic mass or cyst, dilated pancreatic and/or bile duct);
- there is no interest in undergoing treatment of pancreatic neoplasm(s) detected by screening.
- history of chronic kidney disease, serum creatinine > 2.0 mg/dl or estimated glomerulofiltration rate (eGFR) < 30 ml/min, ongoing acute renal failure, cirrhosis of the liver, chronic hepatitis (The estimated glomerulfiltration rate (eGFR) will be calculated based on age, race, and serum creatinine, using the on-line calculator at nephron.com).
- history of dementia
Contacts and Locations| Contact: Hilary Cosby, RN | 410-502-2893 | hcosby1@jhmi.edu |
| United States, Maryland | |
| Johns Hopkins Hospital | Recruiting |
| Baltimore, Maryland, United States, 21205 | |
| Principal Investigator: Marcia Irene F. Canto, MD, MHS | |
| Principal Investigator: | Marcia Irene F. Canto, MD, MHS | Johns Hopkins Medicine |
More Information
No publications provided
| Responsible Party: | Sidney Kimmel Comprehensive Cancer Center |
| ClinicalTrials.gov Identifier: | NCT00714701 History of Changes |
| Obsolete Identifiers: | NCT00084357 |
| Other Study ID Numbers: | J0139 00-04-14-10, J0139 |
| Study First Received: | July 9, 2008 |
| Last Updated: | March 1, 2013 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Neoplasms Pancreatic Neoplasms Digestive System Neoplasms Neoplasms by Site Endocrine Gland Neoplasms Digestive System Diseases |
Pancreatic Diseases Endocrine System Diseases Pancrelipase Gastrointestinal Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 19, 2013