Contrast-enhanced Diffusion-weighted MRI to Detect Liver Metastases in Patients With Pancreatic Cancer (DIA-PANC)
Primary Purpose
Pancreatic Neoplasms
Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Contrast-enhanced Diffusion-weighted MRI
Sponsored by
About this trial
This is an interventional diagnostic trial for Pancreatic Neoplasms focused on measuring Liver metastases, Diffusion weighted MRI
Eligibility Criteria
Inclusion Criteria:
- 18 years and older
- clinical suspicion of pancreatic cancer
- written (signed and dated) informed consent
Exclusion Criteria:
- previous treatment for pancreatic cancer (e.g. chemotherapy, radiotherapy, surgery, ablation therapy)
- concomitant malignancies, except for adequately treated basocellular carcinoma of the skin or in situ carcinoma of the cervix uteri. Subjects with prior malignancies must be disease-free for at least 5 years
- contra-indications to undergo CT (due to e.g. extreme claustrophobia, untreatable contrast allergy, renal function impairment)
- contra-indications to undergo MRI (due to e.g. claustrophobia, untreatable contrast allergy, or not MRI compatible medical devices)
- insufficient command of the Dutch language to be able to understand the patient information or fill in the questionnaires
- pregnancy
Sites / Locations
- Konstantopouleio general hospitalRecruiting
- RadboudumcRecruiting
- Jeroen Bosch ZiekenhuisRecruiting
- Medisch Spectrum TwenteRecruiting
- Universitair Medisch Centrum GroningenRecruiting
- Hospital Universitario Ramón y CajalRecruiting
- InselspitalRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Patients with (suspected) PDAC
Arm Description
Patients with (suspected) pancreatic cancer will undergo additional Contrast-enhanced Diffusion-weighted MRI (CE-DW-MRI) within two weeks from the CECT. Suspected liver lesions on CECT and/or CE-DW-MRI will be biopsied to obtain histopathology as reference standard. For liver lesions without histopathologic proof of metastases a paired follow-up CECT and CE-DW-MRI serve as a composite reference standard. Follow up CECT and CE-DW-MRI will be performed in all patients at 3, 6, and 12 months.
Outcomes
Primary Outcome Measures
Diagnostic accuracy of CE-DW-MRI
Sensitivity and Specificity of CE-DW-MRI for the detection of liver metastases in patients with pancreatic cancer compared to CECT.
Secondary Outcome Measures
Detection of metastasis on CE-DW-MRI in follow-up (3, 6 and 12 months after baseline)
Detection of metastasis with CE-DW-MRI, compared to CECT, in follow-up (3, 6 and 12 months after baseline) of patients with pancreatic cancer, after or during therapy
Assess local resectability
Sensitivity and specificity for CT and MRI to assess local resectability for all patients that underwent surgery
Full Information
NCT ID
NCT03469726
First Posted
February 28, 2018
Last Updated
September 19, 2021
Sponsor
Radboud University Medical Center
Collaborators
Dutch Cancer Society
1. Study Identification
Unique Protocol Identification Number
NCT03469726
Brief Title
Contrast-enhanced Diffusion-weighted MRI to Detect Liver Metastases in Patients With Pancreatic Cancer
Acronym
DIA-PANC
Official Title
Diagnostic Accuracy of Contrast-enhanced Diffusion-weighted MRI for Liver Metastases of Pancreatic Cancer: Towards Adequate Staging and Follow-up of Pancreatic Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 22, 2017 (Actual)
Primary Completion Date
January 1, 2022 (Anticipated)
Study Completion Date
January 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
Dutch Cancer Society
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Given the dismal prognosis of pancreatic cancer, detecting liver metastases early can avoid inappropriate therapy with the associated substantial risks, long-term hospital admissions and high costs, but without survival benefit. The current standard of diagnostic workup with contrast-enhanced CT (CECT) has a poor sensitivity (38-76%) for the detection of liver metastases. As more sophisticated and expensive treatment options emerge, better staging of pancreatic cancer is needed to avoid unnecessary procedures and select the most appropriate treatment strategy. New imaging modalities are available, but their value in staging of pancreatic cancer has not been evaluated yet. Therefore prospective imaging studies are necessary.
The main aim of this study is to determine the diagnostic accuracy of contrast-enhanced diffusion-weighted MRI (CE-DW-MRI) in the detection of liver metastases in patients with pancreatic cancer compared to a reference standard of histopathology and follow up imaging.
The study is an international, multicenter prospective cohort study (inclusion of patients until 138 patients with liver metastases are included, with a total maximum of 465 patients). Patients with pancreatic cancer will undergo additional CE-DW-MRI within two weeks from the CECT. CECT and CE-DW-MRI will be read independently by two radiologists. Suspected liver lesions on CECT and/or CE-DW-MRI will be biopsied to obtain histopathology as reference standard. For liver lesions without histopathologic proof of metastases a paired follow-up CECT and CE-DW-MRI serve as a composite reference standard. Pancreatic resection will be pursued in patients without proven liver or distant metastases. Patients with locally advanced or metastatic disease will be offered palliative treatment. Follow up CECT and CE-DW-MRI will be performed in all patients at 3, 6, and 12 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Neoplasms
Keywords
Liver metastases, Diffusion weighted MRI
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
International multicenter prospective cohort study
Masking
None (Open Label)
Allocation
N/A
Enrollment
465 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Patients with (suspected) PDAC
Arm Type
Other
Arm Description
Patients with (suspected) pancreatic cancer will undergo additional Contrast-enhanced Diffusion-weighted MRI (CE-DW-MRI) within two weeks from the CECT.
Suspected liver lesions on CECT and/or CE-DW-MRI will be biopsied to obtain histopathology as reference standard. For liver lesions without histopathologic proof of metastases a paired follow-up CECT and CE-DW-MRI serve as a composite reference standard. Follow up CECT and CE-DW-MRI will be performed in all patients at 3, 6, and 12 months.
Intervention Type
Diagnostic Test
Intervention Name(s)
Contrast-enhanced Diffusion-weighted MRI
Intervention Description
An MRI scan enhanced with intravenous contrast and with diffusion imaging at several B-values
Primary Outcome Measure Information:
Title
Diagnostic accuracy of CE-DW-MRI
Description
Sensitivity and Specificity of CE-DW-MRI for the detection of liver metastases in patients with pancreatic cancer compared to CECT.
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
Detection of metastasis on CE-DW-MRI in follow-up (3, 6 and 12 months after baseline)
Description
Detection of metastasis with CE-DW-MRI, compared to CECT, in follow-up (3, 6 and 12 months after baseline) of patients with pancreatic cancer, after or during therapy
Time Frame
3, 6 and 12 months
Title
Assess local resectability
Description
Sensitivity and specificity for CT and MRI to assess local resectability for all patients that underwent surgery
Time Frame
Baseline
Other Pre-specified Outcome Measures:
Title
One year survival
Description
Survival rate after 1 year of follow-up
Time Frame
Maximum 1 year
Title
Median survival
Description
Median survival time
Time Frame
Maximum 1 year
Title
Disease free survival
Description
Time without (local) recurrence of cancer in patients that underwent resection
Time Frame
Maximum 1 year
Title
Progression free survival
Description
Time without progression of cancer
Time Frame
Maximum 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years and older
clinical suspicion of pancreatic cancer
written (signed and dated) informed consent
Exclusion Criteria:
previous treatment for pancreatic cancer (e.g. chemotherapy, radiotherapy, surgery, ablation therapy)
concomitant malignancies, except for adequately treated basocellular carcinoma of the skin or in situ carcinoma of the cervix uteri. Subjects with prior malignancies must be disease-free for at least 5 years
contra-indications to undergo CT (due to e.g. extreme claustrophobia, untreatable contrast allergy, renal function impairment)
contra-indications to undergo MRI (due to e.g. claustrophobia, untreatable contrast allergy, or not MRI compatible medical devices)
insufficient command of the Dutch language to be able to understand the patient information or fill in the questionnaires
pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Geke Litjens, MD
Phone
+31243668392
Email
g.litjens@radboudumc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John J. Hermans, dr. ir.
Organizational Affiliation
Radboudumc, Department of Radiology and Nuclear Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kees C.J.H.M. van Laarhoven, prof. dr.
Organizational Affiliation
Radboudumc, Department of Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Konstantopouleio general hospital
City
Athens
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Charikleia Triantopoulou, MD, PhD
Facility Name
Radboudumc
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525GA
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Geke Litjens, MD
Phone
+31243668392
Email
g.litjens@radboudumc.nl
Facility Name
Jeroen Bosch Ziekenhuis
City
Den Bosch
ZIP/Postal Code
5223 GZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Koop Bosscha, MD, PhD
Facility Name
Medisch Spectrum Twente
City
Enschede
ZIP/Postal Code
7512KZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Niels G Venneman, MD, PhD
Facility Name
Universitair Medisch Centrum Groningen
City
Groningen
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Koert de Jong, MD, PhD
Facility Name
Hospital Universitario Ramón y Cajal
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julie Earl, PhD
Facility Name
Inselspital
City
Bern
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adrian Huber, MD, PhD
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32778061
Citation
Litjens G, Riviere DM, van Geenen EJM, Radema SA, Brosens LAA, Prokop M, van Laarhoven CJHM, Hermans JJ. Diagnostic accuracy of contrast-enhanced diffusion-weighted MRI for liver metastases of pancreatic cancer: towards adequate staging and follow-up of pancreatic cancer - DIA-PANC study: study protocol for an international, multicenter, diagnostic trial. BMC Cancer. 2020 Aug 10;20(1):744. doi: 10.1186/s12885-020-07226-0.
Results Reference
derived
Learn more about this trial
Contrast-enhanced Diffusion-weighted MRI to Detect Liver Metastases in Patients With Pancreatic Cancer
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