PET-MRI in Diagnosing Patients With Colon or Rectal Cancer



Status:Recruiting
Conditions:Colorectal Cancer, Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:22 - Any
Updated:1/23/2019
Start Date:April 2013
End Date:November 2020

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Evaluation of PET-MRI in Initial Staging of High Grade Rectal Cancer Patients and in the Follow up of Colorectal Cancer Patients.

This pilot clinical trial studies positron emission tomography (PET)-magnetic resonance
imaging (MRI) and PET-computed tomography (CT) as diagnostic imaging in patients with colon
and/or rectal cancer. New diagnostic imaging procedures, such as PET-MRI, may help find and
diagnose rectal cancer or recurrence of colorectal cancer

PRIMARY OBJECTIVES:

I. To test the diagnostic performance of PET- MRI in the staging of preoperative high-grade
rectal cancer patients, defined by T3 stage or higher or N1 stage or higher or presence of
metastasis, that are referred to PET-CT and MRI.

II. To test the diagnostic performance of PET-MRI the follow up of colorectal cancer patients
that are referred to PET-CT with or without a diagnostic MRI request by their physicians.

SECONDARY OBJECTIVES:

I. To test different attenuation correction MR sequences and novel diagnostic MR sequences.

OUTLINE:

Patients undergo fludeoxyglucose F 18 PET-CT and PET-MRI.

Inclusion Criteria:

- Either having a T3 (the cancer has grown through the muscularis propria and into the
outermost layers of the colon or rectum but not through them) or higher, node
positivity or metastatic lesion in the context of rectal cancer or being studied for
colorectal cancer follow up, independent of the renal function

- PET-CT should be requested by a referring physician; in the case of having an MR
requested as well, it will be reported from the MRI images generated in the PET-MRI

- Stable physical medical conditions to undergo a MRI

- Informed consent must be given and signed prior to study enrollment

Exclusion Criteria:

- Refuse to give and/or sign the informed consent

- Subjects who do not meet the above mentioned inclusion criteria

- Subjects who have a pacemaker

- Subjects who have a metallic prostheses either in the pelvis or in the abdomen that
will interfere with the MR imaging of that anatomical area

- Subjects who suffer from claustrophobia

- Pregnant women

- Cognitive impairment that affects the subject's ability to give consent
We found this trial at
1
site
Cleveland, Ohio 44106
Principal Investigator: Raj Paspulati
Phone: 216-844-1542
?
mi
from
Cleveland, OH
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