ToPanc - Study: Does complete removal of the pancreas in patients with cancer in the head of the pancreas lead to a higher life expectancy than partial removal of the pancreas?
Zusammenfassung der Studie
Certain types of cancer in the head of the pancreas are very aggressive. However, healing is possible through complete surgical removal and additional chemotherapy.
To remove a tumor in the head of the pancreas, partial removal of the pancreas with a connection of the remaining pancreas to the small intestine or stomach is the surgical standard. The worst complication of this operation is the development of a leaking connection with the release of aggressive pancreatic juice into the abdominal cavity, known as a fistula. To avoid the development of a fistula, the entire pancreas can also be removed. Subsequently, the functions of the pancreas (production of digestive enzymes as well as production of insulin and other hormones for blood sugar regulation) must be replaced with medications. This used to be complicated, and patients had a poor quality of life. However, the introduction of new insulin delivery systems has significantly changed this in recent years. Many studies have shown that the quality of life and the complication and mortality rates are now as good as after partial removal.
Our research question is: Is performing a complete pancreas removal in patients at high risk for a postoperative fistula better than just partial removal with a connection of the remaining pancreas? For this purpose, we want to assign patients to a standard group (partial removal of the pancreas) and an intervention group (complete removal of the pancreas). After the operation, many data points such as recovery after surgery, time until the start of chemotherapy, overall survival, and many more will be evaluated. A central point will be the quality of life of the patients regarding blood sugar control.
(BASEC)
Untersuchte Intervention
For our study, we want to assign patients with cancer in the head of the pancreas and a high risk of fistula into two groups:
1. Standard group with partial pancreas removal. This is the current surgical standard for a tumor in the head of the pancreas. During removal, the duodenum and the bile duct running through the head must also be removed. Subsequently, three new connections are sewn to ensure digestion: the remaining pancreas body to the small intestine or stomach, the remaining bile duct to the small intestine, and the stomach outlet to the small intestine. This is an approximately six-hour operation, which leads to complications in about 20-30% of cases even in large centers. One of the worst complications is a leak at the pancreas connection with the outflow of pancreatic juice into the immediate surroundings. This is called a fistula. The juice attacks the surrounding tissue due to its chemical properties, which can lead to severe bleeding and infections, even sepsis. Sometimes, another surgery is necessary, and the remaining pancreas must be removed. Many scientific studies show that patients with such a fistula have worse short- and long-term survival. One reason for this is that patients with such severe complications are often too weak to receive subsequent chemotherapy. Therefore, many surgeons already perform complete removal of the pancreas in cases of a risk situation for a fistula (Point 2).
2. Intervention group with complete pancreas removal. The complete removal of the pancreas has the advantage that the risk of fistula formation is eliminated. Only two instead of three new connections need to be created: one connection from the bile duct to the small intestine and one connection from the stomach to the small intestine. Due to the absence of the pancreas, the dangerous pancreatic fistula can no longer develop. What is often not known is that one can live without a pancreas. However, one is dependent for life on the replacement of digestive enzymes through tablets and insulin through injections or a pump (one is therefore an insulin-dependent diabetic). In the past, blood sugar control was difficult, and the quality of life after such operations was low. Recent developments in automatic, continuous blood sugar monitoring using sensors on the skin and directly connected insulin delivery systems have significantly facilitated diabetes treatment. Several studies have already shown that the quality of life as well as the complication and mortality rates after complete pancreas removal are comparable to the results after partial pancreas removal.
The two main risk factors for a fistula are soft pancreatic tissue and a narrow main duct in the pancreas. Both factors can only be assessed during the operation by the surgeons. If a high risk for the development of a fistula is identified during the operation, patients (who have been informed about the study and have given their consent) can be definitively included in the study. The patients will then be randomly assigned to the standard or intervention group.
It is important to know that surgeons always inform all their patients about the possibility of complete pancreas removal before such a major tumor operation. Furthermore, it has been scientifically proven that both operations are safe and suitable for the treatment of pancreatic cancer.
(BASEC)
Untersuchte Krankheit(en)
This study is dedicated to patients with certain, very aggressive tumors in the area of the head of the pancreas. We focus on so-called adenocarcinomas of the pancreas itself (commonly referred to as 'pancreatic cancer'), cancer of the lower bile duct, and cancer in the area of the opening of the bile duct into the duodenum (so-called papillary carcinomas). For all three types of cancer, both complete tumor removal and subsequent chemotherapy are very important. Only then can healing from these cancers be achieved.
(BASEC)
- At least 18 years old
- Patients for whom a partial pancreas removal is planned due to a high suspicion or proven cancer in the head of the pancreas (so-called ductal adenocarcinomas), cancer of the lower bile duct (so-called cholangiocarcinomas), or cancer in the area of the opening of the bile duct into the duodenum (so-called papillary carcinomas)
- Increased risk for a pancreatic fistula according to international definition (soft pancreatic tissue and narrow main pancreatic duct less than or equal to 3mm)
(BASEC)
Ausschlusskriterien
- Patients with known chronic pancreatitis
- Patients with benign diseases or special tumors (so-called neuroendocrine tumors) of the pancreas
- Pregnancy
(BASEC)
Studienstandort
Aarau, Basel, Bern, Genf, St Gallen, Zürich, Andere
(BASEC)
Baden
(BASEC)
Sponsor
Insel Gruppe AG, Freiburgstrasse 18, 3010 Bern
(BASEC)
Kontakt für weitere Auskünfte zur Studie
Kontaktperson Schweiz
Anna Silvia Wenning
+41 (0)31 632 71 41
annasilvia.wenning@clutterinsel.chInsel Gruppe AG, Freiburgstrasse 18, 3010 Bern
(BASEC)
Allgemeine Auskünfte
Department of Visceral Surgery and Medicine Inselspital, Bern University Hospital,
+41 (0)31 632 71 41;
annasilvia.wenning@clutterinsel.ch(ICTRP)
Allgemeine Auskünfte
Department of Visceral Surgery and Medicine Inselspital, Bern University Hospital
+41 (0)31 632 71 41
annasilvia.wenning@clutterinsel.ch(ICTRP)
Wissenschaftliche Auskünfte
Department of Visceral Surgery and Medicine Inselspital, Bern University Hospital,
+41 (0)31 632 71 41;
annasilvia.wenning@clutterinsel.ch(ICTRP)
Name der bewilligenden Ethikkommission (bei multizentrischen Studien nur die Leitkommission)
Ethikkommission Bern
(BASEC)
Datum der Bewilligung durch die Ethikkommission
26.02.2025
(BASEC)
ICTRP Studien-ID
NCT06801899 (ICTRP)
Offizieller Titel (Genehmigt von der Ethikkommission)
ToPanc Trial: Survival after Total versus partial Pancreaticoduodenectomy for adenocarcinoma of the pancreatic head, distal cholangiocarcinoma, and ampullary cancer: a multi-centric randomized controlled trial. (BASEC)
Wissenschaftlicher Titel
ToPanc Trial: Survival After Total Versus Partial Pancreaticoduodenectomy for Adenocarcinoma of the Pancreatic Head, Distal Cholangiocarcinoma, and Ampullary Cancer: a Multi-centric Randomized Controlled Trial (ICTRP)
Öffentlicher Titel
ToPanc Trial: Survival After Total Versus Partial Pancreaticoduodenectomy for Adenocarcinoma of the Pancreatic Head, Distal Cholangiocarcinoma, and Ampullary Cancer (ICTRP)
Untersuchte Krankheit(en)
Pancreatic Cancer
(ICTRP)
Untersuchte Intervention
Procedure: Total pancreatectomy (TP)Procedure: Partial pancreaticoduodenectomy (PD)
(ICTRP)
Studientyp
Interventional (ICTRP)
Studiendesign
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
(ICTRP)
Ein-/Ausschlusskriterien
Inclusion Criteria:
- Adult patients (age >= 18 years) scheduled to undergo PD for highly suspected or histologically proven, resectable pancreatic ductal adenocarcinoma (PDAC), distal cholangiocarcinoma (DCC), and/or ampullary cancer (pancreaticobiliary type)
- Suspected pancreas anastomosis at high-risk for development of a postoperative pancreatic fistula (POPF) (grade "D" according to Schuh et al. (29): Estimation by CT scan, MRI, and/or Endoscopic Ultrasound
- Written informed consent
Exclusion Criteria:
- Duodenal carcinoma, ampullary cancer (intestinal type), neuroendocrine tumors, benign tumors, chronic pancreatitis
- Medical conditions that do not allow appreciation of the nature, scope, and possible consequences of the trial as judged by the investigator
- Pregnancy. A beta-Human Chorionic Gonadotropin (bHCG) pregnancy test must to be performed for women of child-bearing potential (defined as premenopausal women who have not undergone surgical sterilization)
- Inability to follow the study procedures, e.g., due to psychological disorders, dementia, etc.
(ICTRP)
nicht verfügbar
Primäre und sekundäre Endpunkte
Overall survival (OS)
(ICTRP)
Quality of Life (QoL) Pancreatic Cancer;Quality of Life (QoL) Diabetes;Postoperative complications (discriminating minor and major complications);Mortality;Length of hospital stay in days;Re-admission;Re-operation;Adjuvant Chemotherapy (ACT) initiation;Adjuvant Chemotherapy (ACT) completion;Disease-Free Survival (DFS);Functional status;Body Mass Index (BMI)
(ICTRP)
Registrierungsdatum
nicht verfügbar
Einschluss des ersten Teilnehmers
nicht verfügbar
Sekundäre Sponsoren
nicht verfügbar
Weitere Kontakte
Anna S Wenning, MD, PhD;Anna S Wenning, MD, PhD;Anna S Wenning, MD, PhD, annasilvia.wenning@insel.ch, +41 (0)31 632 71 41;, Department of Visceral Surgery and Medicine Inselspital, Bern University Hospital, (ICTRP)
Sekundäre IDs
2024-02010 (ICTRP)
Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten
nicht verfügbar
Weitere Informationen zur Studie
https://clinicaltrials.gov/study/NCT06801899 (ICTRP)
Ergebnisse der Studie
Zusammenfassung der Ergebnisse
nicht verfügbar
Link zu den Ergebnissen im Primärregister
nicht verfügbar