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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
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pancreatic Adenocarcinoma focused on measuring Adenocarcinoma, pancreas, PET/MRI

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
June 27, 2017
Last Updated
July 24, 2017
Sponsor
Assistance Publique - Hôpitaux de Paris
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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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