DCE-MRI Guided Neoadjuvant Chemotherapy for Borderline Resectable Pancreatic Cancer

Recruiting now · Not applicable

Conditions studied: Borderline-resectable Pancreatic Cancer

In brief

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.

Key facts

Study ID

NCT06173310

Run by

Ohio State University

People needed

50

Starts

2024-10-10

Expected to finish

2029-03-01

Last updated by the study team

2026-02-27

Who can join

Age: 19 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patients (age 19 years or older).
• Patients with newly diagnosed and untreated borderline resectable pancreatic cancer.
• Patients with signed informed consent.

You may not qualify if…

• Any history of prior radiation or chemotherapy or surgical removal for pancreatic cancer.
• Participants with safety contraindications to MRI examination (determined by standard clinical screening).
• Participants who are pregnant, lactating or are planning to become pregnant during the study.
• Participants who are planning to father a child during the study.

Where it is running

• Indiana University Medical Center — Indianapolis, Indiana, United States (enrolling)
• The Ohio State University — Columbus, Ohio, United States (enrolling)

Full record on ClinicalTrials.gov

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