DCE MRI in Patients With Pancreatic Cancer

Pancreatic Adenocarcinoma Clinical Trial

Official title:

The Use of Dynamic Contrast Enhanced Magnetic Resonance Imaging (DCE MRI) in the Management of Pancreatic Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02070705
• Other study ID #: IRB00009694
• Secondary ID: NCI-2014-00270MR
• Status: Recruiting
• Phase: N/A
• Start date: January 31, 2014
• Est. completion date: December 31, 2024

Study information

• Verified date: February 2024
• Source: OHSU Knight Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This clinical trial studies an imaging technique known as dynamic contrast enhanced magnetic resonance imaging (DCE MRI) in identifying the presence of pancreatic cancer. DCE MRI is a procedure that takes detailed pictures of functional and structural properties inside the body using magnetic field imaging. These images may better characterize pancreatic cancer in patients at high risk or in patients who may have undergone chemotherapy for pancreatic cancer.

Description:

PRIMARY OBJECTIVES:

I. Assess the ability of DCE-MRI to identify the presence of pancreatic cancer in patients at high risk for hereditary pancreatic cancer.

II. Assess the ability of DCE-MRI to identify the presence of pancreatic cancer in patients with cystic lesions of the pancreas.

III. Assess the ability of DCE-MRI to accurately predict tumor margins in patients who have undergone chemotherapy for pancreatic cancer.

IV. Obtain DCE-MRI scans of from healthy volunteers (Group 4), to establish baseline imaging parameters of the normal, non-diseased pancreas for use as a comparator to affected pancreata.

SECONDARY OBJECTIVE:

I. Clinical factors associated with the presence of pancreatic cancer will be assessed in each of the three experimental groups, including disease free survival and overall survival.

II. Additional MRI pulses sequences (e.g. MR fingerprinting, etc.) will be acquired for the assessment of tissue contrast before and after the administration of contrast agents.

OUTLINE: Patients are assigned to 1 of 4 groups.

ARM I (High-risk for familial or hereditary pancreatic cancer): Patients undergo DCE MRI yearly for a minimum of 3 scans.

ARM II (Intraductal papillary mucinous neoplasms [IPMN]): Patients undergo DCE MRI prior to surgery for resection of IPMN.

ARM III (Pancreatic cancer): Patients who undergo chemotherapy prior to resection will have 2 DCE MRI scans; one study scan prior to undergoing neoadjuvant therapy, as well as one study scan following neoadjuvant therapy as part of their pre-operative work up in addition to the standard imaging studies. For patients that do not require chemotherapy treatment prior to resection they will have just one DCE MRI scan prior to surgical resection. Patients currently undergoing neoadjuvant therapy or who have already completed neoadjuvant therapy that were unable to undergo imaging at baseline and are now proceeding to resection will have one DCE MRI scan prior to surgical resection.

ARM IV (Healthy volunteers): Patients undergo a single DCE MRI examination.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

• ALL PARTICIPANTS: A negative serum or urine pregnancy test for woman of childbearing potential

• ALL PARTICIPANTS: Ability to understand and the willingness to sign a written informed consent document

• GROUPS 1, 2, AND 3: "All participants" described above

• GROUPS 1, 2, AND 3: Must be consented for the Oregon Pancreatic Tumor Registry (OPTR)

• GROUPS 1, 2, AND 3: Group 1: participants identified as being high-risk for familial or hereditary pancreatic cancer, and must conform to one or more of the following requirements:

• Have a strong family history of pancreatic cancer; this is defined as pancreatic cancer occurring in one first- degree relative and two other relatives, or two first- degree relatives; or,

• Have a known high-risk genetic syndrome (e.g., BRCA 1&2, STK11, CDNK2A, PRSS1, and MSH 2&6)

• GROUPS 1, 2, AND 3: Group 2 participants identified as having IPMN on standard radiographic imaging that meets criteria for resection based on symptoms or on conventional imaging (computed tomography [CT] or MRI) findings

• GROUPS 1, 2, AND 3: Group 3 participants must have pathologically- confirmed pancreatic adenocarcinoma, with or without the need for neoadjuvant chemotherapy prior to surgical resection.

• HEALTHY VOLUNTEERS (Group 4): Must meet inclusion criteria for "all participants" described above

• HEALTHY VOLUNTEERS (Group 4): Group 4 participants must have no history of cancer, pancreatic disease, or family history of pancreatic cancer.

• Family history will be defined as pancreatic cancer occurring in one first-degree relative and two other relatives, or two first-degree relatives

Exclusion Criteria:

• Participants unable or unwilling to give written, informed consent or to undergo MRI imaging

• Participants with multiple drug allergies, and/or subjects who have had an allergic reaction to any intravenous iron replacement product, or a known history of hypersensitivity to ferumoxytol

• Participants with concurrent clinical diagnosis, evidence of suspected hemochromatosis, or other diseases of iron metabolism (i.e., iron overload)

• Cirrhosis, cardiomyopathy, restrictive heart disease, or bronzing of the skin

• Pregnant women are excluded from this study because there is an unknown, but potential risk, for adverse events, as small animal trials have linked ferumoxytol administration (at very high doses) to birth defects (e.g., soft-tissue malformations and decreased fetal weights); it is not known whether ferumoxytol is present in human milk; breastfeeding, however, should be discontinued if the mother receives ferumoxytol while nursing

• Human immunodeficiency virus (HIV)-positive participants on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with ferumoxytol

• Participants with diagnosis of renal insufficiency or glomerular filtration rate (GFR) < 60 ml/min/1.73m^2

• Adult patients who require monitored anesthesia for MRI scanning

• Participants with any contraindications to gadolinium-based contrast agents

• Participants who have a contraindication for MRI (e.g. metal in their bodies, a cardiac pacemaker, or other incompatible device), or are severely agitated or claustrophobic. (For patients that are eligible but there is a concern of metal in their bodies, the will be given the option if interested to have a x-ray completed prior to study enrollment to determine if they can proceed with the study MRI. Patients with a concern of metal in their bodies that don't agree to a x-ray will not be enrolled into the study.)

Related Conditions & MeSH terms

• Familial Pancreatic Cancer
• Neoplasms, Cystic, Mucinous, and Serous
• Pancreatic Adenocarcinoma
• Pancreatic Intraductal Papillary-Mucinous Neoplasm
• Pancreatic Neoplasms

Intervention

Procedure:
• Dynamic Contrast-Enhanced Magnetic Resonance Imaging
Undergo DCE MRI

Drug:
• Ferumoxytol
Given IV

Locations

Country	Name	City	State
United States	OHSU Knight Cancer Institute	Portland	Oregon

Sponsors (5)

Lead Sponsor	Collaborator
OHSU Knight Cancer Institute	National Cancer Institute (NCI), National Institute for Biomedical Imaging and Bioengineering (NIBIB), National Institute for Diabetes and Digestive and Kidney Diseases (NIDDK), Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Presence of pancreatic cancer (yes or no) for patients that are either at high risk for hereditary pancreatic cancer (Group I)	Descriptive statistical analysis will be conducted for primary endpoints.	Up to 5 years
Primary	Presence of pancreatic cancer (yes or no) for patients with cystic lesions of the pancreas (Group II)	Descriptive statistical analysis will be conducted for primary endpoints.	Up to 5 years
Primary	Change in tumor margins in patients who have undergone chemotherapy for pancreatic cancer (Group III)	The change of dynamic contrast enhanced magnetic resonance imaging (DCE MRI) parameters from baseline will be correlated with the tumor margins determined by pathological specimen following surgical resection through linear regression model.	Baseline to up to 2 years
Secondary	Disease free survival (Group I)	Kaplan-Meier method will be used to estimate the survival distribution for disease free survival. The estimated median and 95% confidence interval will be computed.	Time of enrollment to time of diagnosis, assessed up to 5 years
Secondary	Disease free survival (Group II)	Kaplan-Meier method will be used to estimate the survival distribution for disease free survival. The estimated median and 95% confidence interval will be computed.	Time of surgical resection to time of disease recurrence, if applicable, assessed up to 5 years
Secondary	Disease free survival (Group III)	Kaplan-Meier method will be used to estimate the survival distribution for disease free survival. The estimated median and 95% confidence interval will be computed.	Time of surgical resection to time of recurrence, assessed up to 5 years
Secondary	Overall survival (Group I)	Kaplan-Meier method will be used to estimate the survival distribution for overall survival. The estimated median and 95% confidence interval will be computed.	Time of surgical resection to time of death, assessed up to 5 years
Secondary	Overall survival (Group II)	Kaplan-Meier method will be used to estimate the survival distribution for overall survival. The estimated median and 95% confidence interval will be computed.	Time of surgical resection to time of death, assessed up to 5 years
Secondary	Overall survival (Group III)	Kaplan-Meier method will be used to estimate the survival distribution for overall survival. The estimated median and 95% confidence interval will be computed.	Time of surgical resection to time of death, assessed up to 5 years
Secondary	Surgical pathological diagnosis and T & N stage according to the American Joint Committee on Cancer (AJCC) tumor, node, metastasis (TNM) staging system (Group II)	Will be assessed as potential confounders or effect modifiers in the model. Will report c-statistics for each model.	At time of surgery
Secondary	Surgical pathological diagnosis and T & N stage according to the AJCC TNM staging system (Group III)	Will be assessed as potential confounders or effect modifiers in the model. Will report c-statistics for each model.	At time of surgery
Secondary	Resection margin status (R0, R1 or R2) (Group III)	Will be assessed as potential confounders or effect modifiers in the model. Will report c-statistics for each model.	At time of surgery
Secondary	DCE- MRI imaging parameters (Group I)	The DCE- MRI parameters will be obtained from the pancreases in the control group and will be descriptively analyzed for use as a comparison in other groups.	Up to 5 years
Secondary	DCE- MRI imaging parameters (Group II)	The DCE- MRI parameters will be obtained from the pancreases in the control group and will be descriptively analyzed for use as a comparison in other groups.	Once prior to surgery
Secondary	DCE- MRI imaging parameters (Group III)	The DCE- MRI parameters will be obtained from the pancreases in the control group and will be descriptively analyzed for use as a comparison in other groups.	Up to 5 years
Secondary	DCE- MRI imaging parameters and descriptional analysis of normal pancreas DCE- MRI images (Group IV)	The DCE- MRI parameters will be obtained from the pancreases in the control group and will be descriptively analyzed for use as a comparison in other groups.	Once at time of enrollment