Pancreatic adenocarcinoma Pancreatic carcinoma
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: 18 years or older Written informed consent Scheduled for treatment with FOLFIRINOX LAPC defined according to the Dutch Pancreatic Cancer Group Criteria
Exclusion criteria
Exclusion criteria: General MRI contraindications History of allergic reaction to Gadolinium-containing compounds Known renal failure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is the one-year progression free survival of patients with LAPC who received FOLFIRINOX. The research population will be divided into two groups, responders and non-responders. Responders are defined as patients who do not show tumour progression one year after the start of the treatment with FOLFIRINOX. The optimal cut-off value between high and low stiffness will be determined during this study between both groups. From this, the predictive value of MRE on FOLFIRINOX treatment efficacy will be determined. | — |
Secondary
| Measure | Time frame |
|---|---|
| The one and two-year overall survival rate of patients with LAPC who received FOLFIRINOX and its relation to the parameters measured with IVIM and DCE-MRI. | — |
Countries
Netherlands
Outcome results
None listed