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Neoadjuvant Chemotherapy Response Assessment by Combined PET-MRI in Borderline and Locally Advanced Pancreatic Adenocarcinoma.

Neoadjuvant Chemotherapy Response Assessment by Combined PET-MRI in Borderline and Locally Advanced Pancreatic Adenocarcinoma. PACMI (Pancreatic AdenoCarcinoma Multimodality Imaging)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03202199
Acronym
PACMI
Enrollment
125
Registered
2017-06-28
Start date
2017-06-19
Completion date
2021-07-01
Last updated
2017-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Adenocarcinoma

Keywords

Adenocarcinoma, pancreas, PET/MRI

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.

Interventions

DEVICEPET/MRI

2 PET/MRI examinations

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Accuracy of PET/MRI to predict pancreatic adenocarcinoma rescetability after neaadjuvant treatmentPET/MRI performed less than one month before the surgery

Secondary

MeasureTime frame
Accuracy of tumor size, ADC, D, D*, F and SUVmax at baseline, before surgery and their variations for resectabilityPET MRI performed at baseline (15 days before the treatment beginning) less than one month before the surgery
Accuracy of tumor size, ADC, D, D*, F and SUVmax at baseline, before surgery and their variations for response evaluationPET MRI performed at baseline (15 days before the treatment beginning) less than one month before the surgery
Comparison of the accuracies of PT MRI and CT for resectability assessmentCT and PET MRI performed less than one month before the surgery

Countries

France

Contacts

Primary ContactMathilde WAGNER, MD, PhD
mathilde.wagner@aphp.fr0033142178305
Backup ContactOlivier LUCIDARME, MD, PhD
olivier.lucidarme@aphp.fr0033142176322

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026