2025-05
2029-07
2029-07
170
NCT06801899
Insel Gruppe AG, University Hospital Bern
Insel Gruppe AG, University Hospital Bern
INTERVENTIONAL
ToPanc Trial: Survival After Total Versus Partial Pancreaticoduodenectomy for Adenocarcinoma of the Pancreatic Head, Distal Cholangiocarcinoma, and Ampullary Cancer
The goal of this clinical trial is to learn if total removal of the pancreas is a preferable alternative to partial removal in patients with cancer of the pancreatic head who are at high risk of pancreatic leakage. The main question it aims to answer is: Does total pancreas removal improve survival without reducing quality of life compared to partial removal? The only study specific procedures are the collection of 2 blood samples (7.5ml for each time point, preoperatively and during the hospitalisation) and the completion of the questionnaires.
The pancreas is located in the upper abdomen and has 2 main functions: Production of digestive juices and of insulin, the latter being most important for blood sugar regulation and energy conservation. Certain types of cancer in the pancreatic head are very aggressive, but with complete surgical removal of the tumor and additional chemotherapy cure is possible. For tumor resection, the head of the pancreas as well as duodenum and part of the bile duct are removed. 3 new connections are built: the remaining pancreas, bile duct and stomach are connected to a loop of small intestine. This operation takes around 6 hours and leads to complications in 20-30% of cases. A serious complication and unfortunately the most frequent is the leaking of the pancreas remnant, with outflow of the aggressive digestive juice into the surrounding tissue. Consequences may be severe bleeding and/or infections. Many studies show that affected patients have an increased risk of tumor recurrence and a reduced survival. To avoid pancreatic leak, the entire pancreas can be removed. So far, removal of the whole pancreas has only been chosen in cases of very advanced cancer. After both, partial or total pancreas removal, patients need to substitute digestive enzymes. This can be done by capsules, which need to be taken with every meal. But while some patients after partial removal maintain sufficient function to produce insulin, all patients after total removal are diabetic and need insulin injections. In the past, blood sugar control in the absence of insulin production was difficult and accompanied by low quality of life (QoL). This has changed tremendously by the introduction of continuous glucose monitoring (sensors, which are attached to the arm) and automated insulin delivery systems (also known as Ȫrtificial pancreas"). This development renders total pancreas removal a reasonable alternative, with the advantage, that only 2 new connections are made: One between the bile duct and small intestine and one between the stomach and the small intestine. Study question: Is removal of the whole pancreas in patients at high risk of a pancreatic leakage a preferable alternative to partial removal? For this study, patients with cancer of the pancreatic head who are planned for surgery can be included. These patients will be randomly assigned to two groups: 1. Standard group: partial removal of the pancreas 2. Study group: total removal of the pancreas Both techniques are safe and are established techniques to treat cancer in the pancreatic head. After the operation, many clinical data will be recorded. The two most important factors will be survival and quality of life, which will be assessed by questionnaires on a regular base. Additionally, postoperative complications, chemotherapy rates, tumor recurrence and many more data will be monitored.
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates | Results Reporting Dates | Study Record Updates |
---|---|---|
2025-01-24 | N/A | 2025-04-17 |
2025-01-29 | N/A | 2025-04-23 |
2025-01-30 | N/A | 2025-04 |
This section provides details of the study plan, including how the study is designed and what the study is measuring.
Primary Purpose:
Treatment
Allocation:
Randomized
Interventional Model:
Parallel
Masking:
None
Arms and Interventions
Participant Group/Arm | Intervention/Treatment |
---|---|
EXPERIMENTAL: Total pancreatectomy (TP) | PROCEDURE: Total pancreatectomy (TP)
|
ACTIVE_COMPARATOR: Pancreaticoduodenectomy (PD) | PROCEDURE: Partial pancreaticoduodenectomy (PD)
|
Primary Outcome Measures | Measure Description | Time Frame |
---|---|---|
Overall survival (OS) | Number of participants who survived for 2 years after surgery. | At 2 years |
Secondary Outcome Measures | Measure Description | Time Frame |
---|---|---|
Quality of Life (QoL) Pancreatic Cancer | Recorded as participant-reported outcome. Measured by European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire for pancreatic cancer (EORCT QLQPAN26). Scale from 0 to 104, with higher scores indicating a greater level of symptoms or problems. | At 0.5 year, at 1 year, at 2 years |
Quality of Life (QoL) Diabetes | Recorded as participant-reported outcome. Measured by Diabetes Distress Scale (DDS) 17 Questionnaire (only for patients with insulin-dependent diabetes). Scale from 17 to 102, with higher scores indicating a greater level of distress. | At 0.5 year, at 1 year, at 2 years |
Postoperative complications (discriminating minor and major complications) | Number of participants with postoperative complications. Classified according to the Clavien-Dindo-classification (major complication defined as Clavien-Dindo Grade ≥ III). | Within 30 day of surgery |
Mortality | Number of participants who died. | Within 30 days of surgery |
Length of hospital stay in days | Within 30 days of surgery | |
Re-admission | Number of participants who were re-admitted to the hospital. | Within 30 days of surgery |
Re-operation | Number of participants who required a re-operation. | Within 30 days of surgery |
Adjuvant Chemotherapy (ACT) initiation | Number of days from surgery to ACT initiation. | At 1 year |
Adjuvant Chemotherapy (ACT) completion | Number of days from surgery to ACT completion. | At 1 year |
Disease-Free Survival (DFS) | Number of participants who remained free of disease. Defined as no new metastasis or local recurrence on CT or MRI imaging, and, if applicable, laboratory tests (new Ca19-9 increase). | At follow-up, up to 4.5 years |
Functional status | Recorded as participant-reported outcome. Measured by Eastern Cooperative Oncology Group (ECOG) Performance Status Scale. Scale from 1 to 5, with higher scores indicating a greater level of disability. | At 0.5 year, at 1 year, at 2 years |
Body Mass Index (BMI) | At 0.5 year, at 1 year, at 2 years |
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact Name: Anna S Wenning, MD, PhD Phone Number: +41 (0)31 632 71 41 Email: annasilvia.wenning@insel.ch |
Study Contact Backup Name: Nadine Uebersax Phone Number: +41 (0)31 684 33 69 Email: nadine.uebersax@unibe.ch |
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.
Ages Eligible for Study:
ALL
Sexes Eligible for Study:
18 Years
Accepts Healthy Volunteers:
This is where you will find people and organizations involved with this study.
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
No publications available
NPCF was founded on May 29, 2009 and is a 501(c)(3) organization. All donations are tax deductible.
The information and services provided by the National Pancreatic Cancer Foundation are for informational purposes only. The information and services are not intended to be substitutes for professional medical advice, diagnosis or treatment. The National Pancreatic Cancer Foundation does not recommend nor endorse any specific physicians, products or treatments even though they may be mentioned on this site.