DCE-MRI Guided Neoadjuvant Chemotherapy for Borderline Resectable Pancreatic Cancer

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.

Interventions

• Point-of-care Portable Perfusion Phantom (P4) · DEVICE

  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.

Published eligibility criteria

Verbatim from the registry. Only the site can decide how these apply to a specific patient.

Inclusion Criteria:

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

Exclusion Criteria:

* 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.

Sites (2)

• Indiana University Medical Center, Indianapolis, Indiana · RECRUITING
• The Ohio State University, Columbus, Ohio · RECRUITING