Actively Recruiting
Efficacy and Safety of TPIAT for Resectable Adenocarcinoma of the Pancreas Region at High Risk of Postoperative Fistula
Led by University Hospital, Lille · Updated on 2025-09-25
36
Participants Needed
1
Research Sites
417 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Lille
Lead Sponsor
M
Ministry of Health, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
Curative management of locally resectable invasive adenocarcinomas located in the cephalic region of the pancreas (pancreas, duodenum and ampulla of Vater) requires a pancreaticoduodenectomy followed by adjuvant chemotherapy. Pancreaticoduodenectomy is a major surgery that often leads to major complications including approximately 20% of relevant clinical postoperative pancreatic fistula. Postoperative complications following pancreaticoduodenectomy can lead to early discontinuation of the complete oncologic strategy, i.e., chemotherapy for malignancy is performed in only about a third of patients who experienced a grade C fistula. A total pancreatectomy rather than a pancreaticoduodenectomy is an alternative procedure that involves the complete and definitive resection of all pancreatic tissue, eliminating any risk of postoperative pancreatic fistula but is associated with unavoidable endocrine insufficiency and potentially severe metabolic complications, such as "brittle diabetes". Total Pancreatectomy following by intraportal Islet AutoTransplantation (TPIAT) can prevent "brittle diabetes" and improve the quality of life. The endocrine islets can be isolated from the pancreatic surgical specimen with standardized procedures and transplanted in the liver through intraportal infusion, in absence of immunosuppression and allow adequate control of glucose metabolism with a reduced need for exogenous insulin and an effective graft function in 70% of cases at 3 years Thereby, the investigators hypothesize that total pancreatectomy with intraportal Islet autotransplantation rather than classical pancreaticuduodenectomy, in patients with high-risk of postoperative fistula will increase the rate of complete access to adjuvant chemotherapy, while maintaining an adequate metabolic control.
CONDITIONS
Official Title
Efficacy and Safety of TPIAT for Resectable Adenocarcinoma of the Pancreas Region at High Risk of Postoperative Fistula
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Locally resectable invasive adenocarcinomas in the cephalic region of the pancreas, duodenum, or ampulla of Vater confirmed by endoscopic ultrasonography with biopsy
- Diagnosis includes pancreatic adenocarcinoma, duodenal adenocarcinoma, ampullary adenocarcinoma, or IPMNs with adenocarcinoma degeneration
- Approved curative strategy with primary tumor resection by a multidisciplinary expert team
- High risk of clinically relevant postoperative pancreatic fistula (CR-POPF) as indicated by at least two factors among male sex, obesity (BMI ≥ 30 kg/m2), main pancreatic duct diameter ≤ 3 mm, visceral obesity, or sarcopenia
- Intraoperative confirmation of high risk with a probability score ≥ 20% on the updated alternative Fistula Risk Score
- Women of childbearing potential must have a confirmed menstrual period, negative pregnancy test, and agree to monthly pregnancy testing during chemotherapy
- Both women of childbearing potential and men must agree to use highly effective contraception during chemotherapy and for specified periods after
- Patient covered by a health insurance system
- Patient provides written informed consent to participate
You will not qualify if you...
- Preoperative diabetes with stimulated C-peptide < 0.5 ng/mL relative to blood glucose > 2 g/dL at 2 hours postprandial
- Known or suspected genetic syndromes associated with pancreatic adenocarcinoma risk such as familial pancreatic cancer, Peutz-Jeghers syndrome, hereditary chronic pancreatitis, cystic fibrosis, familial breast/ovarian cancer, Lynch syndrome, adenomatous polyposis family, Li Fraumeni syndrome, or multi-endocrine disorder type I
- Multifocal pancreatic adenocarcinomas identified before surgery
- Poor performance status or comorbidity profile unsuitable for major abdominal surgery
- Contraindications for autologous islet intraportal transplantation
- Current or planned neoadjuvant chemotherapy
- Presence of extra pancreatic metastasis found in imaging or during surgery
- Need for major vein reconstructions during surgery
- Macroscopic or biological evidence of post biliary drainage pancreatitis that affects islet isolation
- Known infections or positive serology for HIV, Hepatitis B or C, HTLV, or syphilis
- Active SARS-CoV-2 infection requiring delayed intervention
- Pregnant or breastfeeding women
- Total deficiency of dihydropyrimidine dehydrogenase
- Inability to understand study purposes or provide informed consent
- Inability to comply with study schedule
- Not covered by health insurance
- Detained, receiving psychiatric care, or admitted to social or medical sanatorium
- Emergency situations
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hop Claude Huriez Chu Lille
Lille, France, 59037
Actively Recruiting
Research Team
F
François PATTOU, MD,PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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