Pancreatic Cancer Screening for At-risk Individuals (The Pancreas Scan Study)
Overview
- Phase
- N/A
- Intervention
- Screening for pancreatic cancer
- Conditions
- Pancreatic Cancer, Adult
- Sponsor
- Beth Israel Deaconess Medical Center
- Enrollment
- 1395
- Locations
- 2
- Primary Endpoint
- Proportion of screening patients found to have high-risk pancreatic lesions amenable to treatment
- Status
- Recruiting
- Last Updated
- 10 days ago
Overview
Brief Summary
The investigators' goal is to conduct a prospective multicenter study to evaluate the yield and outcomes of screening of pancreas cancer in individuals who are at-risk for pancreatic cancer. We plan to use International Cancer of the Pancreas Screening (CAPS3) Consortium recommendations to standardize study population, screening methodology, and study outcomes.
Detailed Description
Methods The investigators' goal is to conduct a prospective multicenter study to evaluate the yield and outcomes of pancreas cancer screening in high-risk individuals. High-risk patients who are undergoing pancreatic cancer screening in accordance with national guidelines at participating study centers will be eligible for the study. Information regarding patient characteristics, findings at screening examination, and patient outcomes will be collected. Primary Outcome (Primary Aim): To identify the proportion of patients who meet International Cancer of the Pancreas Screening Consortium screening criteria 3rd update (CAPS Jan 2020), or more updated national guidelines, who are found at the screening to have high-risk pancreatic lesions amenable to treatment (definition of "high-risk lesions amenable to treatment" is provided under the section on study outcomes). Secondary outcomes (Secondary Aims) will include (details are provided under the section on study outcomes): 1. Proportion of patients diagnosed with any stage pancreatic cancer 2. proportion of patients undergoing pancreatic surgery 3. Cancer-related outcome, defined as a cancer-related death 4. proportion of patients experience harms, defined as any complications/adverse event due to screen related procedures 5. Comparison of cancer outcome, defined cancer-related death, in screen-detected cancer with cancer outcomes reported by the SEERs population-based registry. Study overview Study type: a prospective observational cohort High-risk patients who meet study inclusion criteria at study centers will be identified. Screening and patient follow-up will be performed at individual study centers per standard clinical practice. Patient characteristics, screening performed and screening results, clinical outcome data will be collected by individual study centers. This data will be stored and analyzed at central study REDCap located at Beth Israel Deaconess Medical Center (BIDMC)
Investigators
Mandeep Sawhney
Co-Director for GI Endoscopy & Director for Endoscopy Research, BIDMC
Beth Israel Deaconess Medical Center
Eligibility Criteria
Inclusion Criteria
- •Inclusion criteria 1-3 are indications for pancreatic cancer screening as defined by the CAPS3 guidelines or updated national pancreatic cancer screening guidelines. Patients who do not meet these guidelines but are undergoing pancreatic cancer screening at the discretion of their treating physician at participating study centers will also be included in the study. Based upon the indication for screening, patients will be categorized as either meeting CAPS3 screening criteria, or not meeting CAPS3 screening criteria.
- •Familial Pancreatic cancer kindred. This is defined as family history of pancreas cancer that meet the criteria listed below.
- •If at least two affected relatives who are First degree relatives (FDR) to each other, of whom at least one is an FDR to the individual considered for surveillance
- •If at least three affected relatives on the same side of the family, of whom at least one is an FDR to the individual considered for surveillance
- •If at least two affected relatives on the same side of the family, of whom at least one is an FDR to the individual considered for surveillance Screening is usually initialed at age 50 years or 10 years younger than the youngest family member with pancreatic cancer
- •Patients with genetic susceptibility to pancreas cancer
- •Patients with Peutz-Jeghers syndrome diagnosed with using clinical criteria or with a deleterious mutation in liver kinase B1/Serine/threonine kinase 11 (LKB1/STK11). Screening is usually initiated at age 40 years or later.
- •Patients with Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM syndrome), diagnosed using clinical criteria or CDKN2A p16 mutation.
- •Screening is usually initiated at age 45 years or 10 years younger than the youngest family member with pancreatic cancer.
- •Hereditary Breast and Ovarian Cancer syndrome: diagnosed using clinical criteria or deleterious Breast Cancer gene 1 (BRCA1), Breast Cancer gene 2 (BRCA2), Partner and Localizer of BRCA2 (PALB2). The usual indication for screening is:
Exclusion Criteria
- •Patients presenting with symptoms suggestive of pancreatic cancer who are undergoing diagnostic EUS or MRCP e.g. acute recurrent pancreatitis, abnormal imaging
Arms & Interventions
Patients who are at high-risk for pancreatic cancer
Patients that meet the eligibility criteria based on CAPS3 or updated national pancreatic cancer screening guidelines
Intervention: Screening for pancreatic cancer
Outcomes
Primary Outcomes
Proportion of screening patients found to have high-risk pancreatic lesions amenable to treatment
Time Frame: From year 1 to year 12 (until the end of at least 5 years follow up in 2032), according to the standard of care designated by GI team.
Proportion of patients who meet CAPS 3 or updated national screening guidelines criteria who are found at screening to have high-risk pancreatic lesions amenable to treatment. These are defined as the following: Lesions with high-grade dysplasia (HGD), High-grade pancreatic intraepithelial neoplasia (PanIN), Resectable or borderline resectable pancreatic cancer. Pancreatic cancers that were staged T1-3, N0-2, and M0 designated as resectable or borderline resectable. Cancers that were staged as T4 or M1 were considered locally advanced or metastatic and therefore designated as unresectable, Main duct intra-ductal papillary mucinous neoplasm (IPMN)., Branch-duct IPMN with "worrisome features", cyst associated with an abrupt change in main pancreatic duct caliber with pancreatic atrophy, Neuroendocrine tumor ≥ 2 cm.
Secondary Outcomes
- Proportion of screening patients found to have high-risk pancreatic lesions(From year 1 screening to year 12 (end of at least 5 years follow up in 2032) screening (annually))
- Proportion of screening patients found to have low or moderate-risk pancreatic lesions by screening(From year 1 to year 12 (end of at least 5 years follow up in 2032) according to the standard of care designated by GI team.)
- Proportion of patients undergoing screening who undergo pancreatic surgery(From year 1 to year 12, which is the end of at least 5 years follow up in 2032.(throughout the duration of the study))
- Proportion of "low yield" pancreatic surgeries performed in screening patients(From year 1 to year 12, which is the end of at least 5 years follow up in 2032.(throughout the duration of the study))
- Proportion of screening patients who undergo non-pancreatic surgery(From year 1 to year 12 (the end of at least 5 years follow up in 2032), according to the standard of care designated by GI team)
- Proportion of screening patients who experience complications/adverse events of screen-related procedures(From year 1 to year 12 (the end of at least 5 years follow up in 2032), according to standard of care designated by GI team)