A Study of Magnetic Resonance Imaging of the Pancreas for Cancer Screening

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The purpose of this study is to develop a dedicated MRI scan of the pancreas (MRP) to better detect pancreatic cancer in people who are at a high risk for pancreatic cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Two first-degree relatives with pancreas cancer, one being a first-degree relative to the individual

Pathogenic mutation in APC, BRCA1, MLH1, MSH2, MSH6, PMS2, EPCAM, PALB2, or TP53 and a first/second-degree relative with pancreas cancer

Pathogenic mutation in CDKN2A/p16, STK11, PRSS1, SPINK1/PST1, CTRC, CPA1, ATM, or BRCA2

Meets surveillance age eligibility, which is typically age 50, or 10 years earlier than the youngest relative with pancreas cancer. For individuals with certain gene mutations, this can be earlier. All participants must be aged 21+

Disqualifiers

None

Trial population

Investigators will conduct this pilot study in high-risk individuals enrolled in the Memorial Sloan Kettering Pancreatic Tumor Registry

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • MRI

    Diagnostic test

    Participants will undergo a single MRI of the abdomen without contrast

  • Endoscopic ultrasound

    Diagnostic test

    EUS will be scheduled the same day or within 2 weeks prior to MRP

Treatment groups

79 Participants
are divided into 1 treatment group
Group A: Participants at high risk for pancreas ductal adenocarcinoma2 interventions

Trial outcomes

Primary outcomes

1

Compare image quality of novel high-resolution magnetic resonance pancreas (MRP) to conventional MRCP

Develop and pilot a focused high-resolution magnetic resonance pancreas (MRP) exam to help facilitate early pancreatic cancer detection in high-risk individuals. Image quality for T1, T2, and DWI sequences performed on the novel MRP exam will be compared to conventional MRCP performed in the same participants.

Time frame
Up to 3 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Memorial Sloan Kettering Cancer Center

Lead sponsor

National Institutes of Health (NIH)

Collaborator