About this trial
Induction mFOLFIRINOX has become the standard in the management of locally advanced and borderline adenocarcinoma. Following the results of the PREOPANC-01 JASP-05, NEONAX studies it is expected that the neoadjuvant approach will be the standard strategy soon in patients with resectable PAC. The results of the PANACHE-01 trial confirm the feasibility of the neoadjuvant approach in the setting of resectable adenocarcinoma. Two randomized phase III studies, on the same design as PANACHE-01 are currently underway comparing neoadjuvant and adjuvant chemotherapy with mFOLFIRINOX for resectable PAC, (Alliance AO21806, NCT04340141; PREOPANC3, NCT04927780). Despite the improvement of oncosurgical management, recurrence of PAC soon after resection occurs frequently, leading to the dismal prognosis and unnecessary surgery-related loss of quality of life. Thus, there is urgent need for development of innovative and new strategies to decrease postoperative recurrence.
Important residual tumor load after NAT suggests a primary resistance of the tumor or the selection of resistant clones. The most innovative aspect of this study will be to adapt the adjuvant chemotherapy strategy to the pathological response (downstaging) in patients who will have R0-R1 resection after neoadjuvant mFOLFIRINOX, taking into account the chemoresistance/sensibility status of the tumor.
Eligibility criteria
Qualifiers
Histologically confirmed resected pancreatic adenocarcinoma (R0 or R1) that has received 3 months of neoadjuvant mFOLFIRINOX, including anatomically resectable and borderline resectable tumors, in accordance with the definitions and therapeutic considerations provided in the TNCD (2024) and ESMO (2023) guidelines.
Performance status ECOG 0 or 1
CA 19-9 level ≤ 200 U/ml
Age 18 years or over
Disqualifiers
Metastatic PAC on post-operative imaging
Cholangiocarcinoma, ampullary carcinoma or other non-PAC pancreatic tumors
Non-controlled congestive heart failure, non-treated angina, recent myocardial infarction (in the previous year), non-controlled AHT (SBP > 160 mm Hg or DBP > 100 mm Hg, despite optimal drug treatment), long QT
Major non-controlled infection, chronic infectious diseases, immune deficiency syndromes
Trial design
Treatments tested in this trial
- Gem/Nabpaclitaxel infusion
- mFOLFIRINOX infusion
Treatment groups
Sponsors and collaborators
University Hospital, Rouen
Lead sponsor
Partenariat de Recherche en Oncologie DIGEstive - PRODIGE
Collaborator
Federation de recherche en chirurgie digestive (FRENCH)
Collaborator