Neoadjuvant Chemotherapy Response Assessment by Combined PET-MRI in Borderline and Locally Advanced Pancreatic Adenocarcinoma. (PACMI)
Primary Purpose
Pancreatic Adenocarcinoma
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
PET/MRI
Sponsored by
About this trial
This is an interventional diagnostic trial for Pancreatic Adenocarcinoma focused on measuring Adenocarcinoma, pancreas, PET/MRI
Eligibility Criteria
Inclusion Criteria:
- Age > 18yo
- Locally advanced or borderline resectable pancreatic adenocarcinoma, according to the NCCN classification
- Eligible for neoadjuvant chemotherapy ± radiation therapy, according to the local tumor board
- With contraception if fertile woman
- With informed consent obtained
- Affiliated to French health care system
Exclusion Criteria:
- Previous treatment for the pancreatic adenocarcinoma
- Metastases
- Contra-indication to MRI acquisition (pace maker, metallic device, ..)
- Contra-indication to PET acquisition (non controlled diabetes with glycaemia > 11 mmol/L)
- Pregnancy or breast feeding
- Patient unable to give his consent
Sites / Locations
- Pitié Salpetriere HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
PET/MRI
Arm Description
PET/MRI examination
Outcomes
Primary Outcome Measures
Accuracy of PET/MRI to predict pancreatic adenocarcinoma rescetability after neaadjuvant treatment
Secondary Outcome Measures
Accuracy of tumor size, ADC, D, D*, F and SUVmax at baseline, before surgery and their variations for resectability
Accuracy of tumor size, ADC, D, D*, F and SUVmax at baseline, before surgery and their variations for response evaluation
Comparison of the accuracies of PT MRI and CT for resectability assessment
Full Information
NCT ID
NCT03202199
First Posted
June 27, 2017
Last Updated
July 24, 2017
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT03202199
Brief Title
Neoadjuvant Chemotherapy Response Assessment by Combined PET-MRI in Borderline and Locally Advanced Pancreatic Adenocarcinoma.
Acronym
PACMI
Official Title
Neoadjuvant Chemotherapy Response Assessment by Combined PET-MRI in Borderline and Locally Advanced Pancreatic Adenocarcinoma. PACMI (Pancreatic AdenoCarcinoma Multimodality Imaging)
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Unknown status
Study Start Date
June 19, 2017 (Actual)
Primary Completion Date
January 1, 2020 (Anticipated)
Study Completion Date
July 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
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
The aim of this study was to assess the diagnostic accuracy of PET-MRI to predict resectability of pancreatic adenocarcinoma after neoadjuvant chemotherapy ± radiation therapy.
Detailed Description
Background: Pancreatic cancer is the 8th more common cancer in the world. At diagnosis, majority of patients present with unresectable locally advanced disease. Standard of care therapy for locally advanced pancreatic cancer includes chemotherapy ± radiation therapy. It is published that computed tomography underestimate the effectiveness of neoajuvant treatment and there is a lack of criteria allowing identifying the responders. The misinterpretation of scans may be linked to the large desmoplatic reaction, present in pancreatic cancer, which would not be expected to regress. PET-MR is an imaging technique that associates PET and MR imaging, performed during the same examination. The main hypothesis is that PET-MR imaging could accurately identify resectable and no resectable pancreatic adenocarcinoma after neoadjuvant chemotherapy ± radiation therapy.
Primary aim Assess the diagnostic accuracy of PET-MRI to predict resectability of pancreatic adenocarcinoma after neoadjuvant chemotherapy ± radiation therapy
Secondary aims Assess the accuracy of quantitative PET-MRI parameters to predict resectability and response of pancreatic adenocarcinoma after neoadjuvant chemotherapy ± radiation therapy Compare accuracy of PET-MRI and CT to predict resectability of pancreatic adenocarcinoma after neoadjuvant chemotherapy ± radiation therapy.
Assess inter and intra observer reproducibility of PET-MRI reading CT to predict resectability of pancreatic adenocarcinoma after neoadjuvant chemotherapy ± radiation therapy.
Number of subjects 125 Number of centers 8
Design 2 PET-MRI examination will be performed, one before the beginning of the neoadjuvant/induction treatment, and the second one after the neoadjuvant/induction treatment and less than 30 days before the surgery. The PET-MRI examinations will include whole body and organ specific imaging.
The whole body workflow will include
[18F]-2-fluoro-2-deoxy-D-glucose PET acquisition
T1-mDIXON imaging (for attenuation correction calculation)
diffusion-weighted imaging
T1-DIXON imaging post gadolinium chelate injection. The organ specific workflow will be focused on the abdominal area, including the liver and the pancreas, and will include
[18F]-2-fluoro-2-deoxy-D-glucose PET acquisition,
T2-weighted imaging with and without fat saturation,
T1-DIXON imaging before and after dynamic injection of gadolinium chelate,
diffusion-weighted imaging,
IVIM-diffusion weighted imaging acquisition covering the pancreatic lesion. Qualitative analysis of PET-MRI using a Likert score will be compared to pathological results in order to obtain the accuracy of PET-MRI for resectability assessement.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Adenocarcinoma
Keywords
Adenocarcinoma, pancreas, PET/MRI
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
125 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
PET/MRI
Arm Type
Experimental
Arm Description
PET/MRI examination
Intervention Type
Device
Intervention Name(s)
PET/MRI
Intervention Description
2 PET/MRI examinations
Primary Outcome Measure Information:
Title
Accuracy of PET/MRI to predict pancreatic adenocarcinoma rescetability after neaadjuvant treatment
Time Frame
PET/MRI performed less than one month before the surgery
Secondary Outcome Measure Information:
Title
Accuracy of tumor size, ADC, D, D*, F and SUVmax at baseline, before surgery and their variations for resectability
Time Frame
PET MRI performed at baseline (15 days before the treatment beginning) less than one month before the surgery
Title
Accuracy of tumor size, ADC, D, D*, F and SUVmax at baseline, before surgery and their variations for response evaluation
Time Frame
PET MRI performed at baseline (15 days before the treatment beginning) less than one month before the surgery
Title
Comparison of the accuracies of PT MRI and CT for resectability assessment
Time Frame
CT and PET MRI performed less than one month before the surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > 18yo
Locally advanced or borderline resectable pancreatic adenocarcinoma, according to the NCCN classification
Eligible for neoadjuvant chemotherapy ± radiation therapy, according to the local tumor board
With contraception if fertile woman
With informed consent obtained
Affiliated to French health care system
Exclusion Criteria:
Previous treatment for the pancreatic adenocarcinoma
Metastases
Contra-indication to MRI acquisition (pace maker, metallic device, ..)
Contra-indication to PET acquisition (non controlled diabetes with glycaemia > 11 mmol/L)
Pregnancy or breast feeding
Patient unable to give his consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mathilde WAGNER, MD, PhD
Phone
0033142178305
Email
mathilde.wagner@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Olivier LUCIDARME, MD, PhD
Phone
0033142176322
Email
olivier.lucidarme@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mathilde WAGNER, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pitié Salpetriere Hospital
City
Paris
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mathilde WAGNER, MD, PhD
Phone
0033142178305
Email
mathilde.wagner@aphp.fr
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Neoadjuvant Chemotherapy Response Assessment by Combined PET-MRI in Borderline and Locally Advanced Pancreatic Adenocarcinoma.
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