RecruitingNot ApplicableNCT06173310

DCE-MRI Guided Neoadjuvant Chemotherapy for Borderline Resectable Pancreatic Cancer


Sponsor

Ohio State University

Enrollment

50 participants

Start Date

Oct 10, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this study is to test whether chemotherapy guided by a new imaging method named DCE-MRI can more effectively reduce a pancreatic tumor, enabling curable surgery, over the conventional method when a tumor is categorized as borderline resectable pancreatic cancer. UAB radiological research team has been studying a cutting-edge imaging technique named dynamic contrast-enhanced magnetic resonance imaging, or DCE-MRI, for over 10 years. This technique has been globally used to calculate the blood flow of various tissues, including tumors. Blood flow often serves as a critical indicator showing a disease status. For example, a pancreatic tumor typically has low blood flow, so it can be used as an indicator to identify the presence of a pancreatic tumor. In addition, an effective therapy can result in the increase of blood flow in a pancreatic tumor during the early period of treatment. Therefore, the investigators may be able to determine whether the undergoing therapy is effective or not by measuring the change of blood flow in the pancreatic tumor and deciding whether to continue the therapy or try a different one.


Eligibility

Min Age: 19 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether a special type of MRI scan (called DCE-MRI, which measures blood flow in tumors) can help doctors decide how much chemotherapy to give before surgery for borderline resectable pancreatic cancer — meaning cancer that sits right on the edge of being removable. **You may be eligible if...** - You are 19 years or older - You have been newly diagnosed with borderline resectable pancreatic cancer (cancer near key blood vessels but potentially removable with surgery) - You have not yet had any treatment for your pancreatic cancer (no chemotherapy, radiation, or prior surgery) - You are able to have an MRI scan **You may NOT be eligible if...** - You have had prior treatment for pancreatic cancer - You have a safety reason that prevents you from having an MRI (such as a pacemaker or certain metal implants) - You are pregnant, breastfeeding, or planning to become pregnant Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEPoint-of-care Portable Perfusion Phantom (P4)

P4 is a perfusion phantom developed by Dr. Harrison Kim that can significantly reduce variation in quantitating perfusion of human abdominal tissues across MRI scanners.


Locations(2)

Indiana University Medical Center

Indianapolis, Indiana, United States

The Ohio State University

Columbus, Ohio, United States

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NCT06173310


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