UCSF PCR: UCSF Panc Cyst Registry

Sponsor
University of California, San Francisco (Other)
Overall Status
Recruiting
CT.gov ID
NCT04291651
Collaborator
Eureka (Other)
4,000
1
122.8
32.6

Study Details

Study Description

Brief Summary

Pancreatic cysts are found incidentally on 15-50% of CT and MRIs for all indications and their prevalence is increasing. Many of these cysts may be precursors to pancreatic cancer, and thus pose a substantial risk, however, the vast majority are benign. Increased detection of pancreatic cysts provides an opportunity to diagnose pancreatic malignancy at an early, curable stage yet also increases the potential to over-treat clinically insignificant lesions. This presents a clinical challenge to prevent unnecessary resection of indolent disease, with associated risks of infections, bleeding, diabetes, and costly disability. Unfortunately, there is little information on the epidemiology and natural history of pancreatic cysts to help guide management. This study develops a large, prospectively managed, electronic, patient-directed pancreatic cyst registry based at UCSF using the NIH-funded Eureka Health platform. PANC Cyst will facilitate work to improve clinical care and understanding of pancreatic cysts by prospective follow-up of patients with cystic lesions, especially the diagnostically challenging small cysts, to identify factors related to cyst formation and progression to malignancy. Longitudinal data capture that includes clinical outcomes will also enable us to more precisely define anatomic, radiographic and biomarker information that can be used to differentiate populations of patients for whom surgery is indicated, surveillance is warranted, or no further evaluation is necessary.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
4000 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Population-Based Analysis of Neoplastic Changes in Cystic Lesions of the Pancreas.
Actual Study Start Date :
Oct 8, 2019
Anticipated Primary Completion Date :
Jan 1, 2030
Anticipated Study Completion Date :
Jan 1, 2030

Arms and Interventions

Arm Intervention/Treatment
Retrospective

The registry will be populated with a retrospective cohort of patients previously identified as having pancreatic cysts.

Prospective

The prospectively enrolled patients in this study are the primary population of interest.

Other: Survey
There are no study-specific interventions, as this is a prospective registry. However, patients will be asked to complete approximately 1-2 hours worth of surveys on things such as demographics, medical and surgical history, and pancreatic cyst-specific questionnaires.

Outcome Measures

Primary Outcome Measures

  1. Cancer [1-10 years]

    While not the primary outcome measure, the development of cancer from a pancreatic cyst is a critically important study endpoint, which the investigators do not expect to be frequent occurrence.

  2. Indolency [1-10 years]

    If a patient with a pancreatic cyst experiences no or minimal change in size, and no development of worrisome or high-risk stigmata (Tanaka 2017), this will be considered to be an indolent lesion. Most patients will fall under this category.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • The inclusion criteria for this study are intentionally broad. Eligible patients for prospective enrollment will include

  • Adults ≥ 30 years of age

  • Have a radiographic or endoscopic diagnosis of at least one pancreatic cysts regardless of treatment status,

  • No history of pancreatic cancer,

  • Can speak and read English,

  • Have access to a computer or mobile device (~95% of U.S. population); and

  • Are able to complete an electronic informed consent.

Exclusion Criteria:
  • Patients who don't speak English,

  • Don't have access to a computer or mobile device; or

  • Patients who have a cancer diagnosis.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCSF Medical Center San Francisco California United States 94158

Sponsors and Collaborators

  • University of California, San Francisco
  • Eureka

Investigators

  • Principal Investigator: Kimberly S Kirkwood, MD, University of California, San Francisco
  • Principal Investigator: Paige M Bracci, PhD, MPH, MS, University of California, San Francisco

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT04291651
Other Study ID Numbers:
  • 17-23574
First Posted:
Mar 2, 2020
Last Update Posted:
Sep 1, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of California, San Francisco
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 1, 2021