Minimally Invasive Pancreatic Enucleation With Main Pancreatic Duct Repair or Reconstruction
Pancreatic Tumor, Benign, Pancreatic Neuroendocrine Tumor, Solid Pseudopapillary Tumor of the Pancreas
About this trial
This is an interventional treatment trial for Pancreatic Tumor, Benign focused on measuring Pancreatic benign or low-grade malignant tumors, Minimally invasive enucleation, Main Pancreatic Duct Repair or Reconstruction, Long-term prognosis, Quality of life
Eligibility Criteria
Inclusion Criteria: Age between 18 and 70 years, regardless of gender. Solitary benign or low-grade malignant tumor of the pancreas. Patients evaluated according to guidelines indicating the need for surgery or strongly requesting surgery. Feasibility of performing minimally invasive pancreatic tumor enucleation based on preoperative imaging evaluation. Intraoperative procedure involving repair or reconstruction of the main pancreatic duct. Patients with an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. Willingness to comply with the study's follow-up plan and other protocol requirements. Voluntary participation and signed informed consent. Exclusion Criteria: Body mass index (BMI) > 35 kg/m2. Individuals planning pregnancy, currently pregnant, or breastfeeding. History of major abdominal surgery. Concurrent presence of other malignant tumors. Intraoperative frozen pathology or postoperative pathology indicating the tumor to be malignant, requiring curative resection instead. Severe impairment of cardiac, hepatic, or renal function (e.g., NYHA class 3-4 heart failure, ALT and/or AST levels exceeding three times the upper limit of normal, creatinine levels exceeding the upper limit of normal). Participation in other clinical trials simultaneously. Withdrawal Criteria: Significant changes in the participant's condition after enrollment that render the study protocol unsuitable or infeasible. Occurrence of severe complications that impact the implementation of the study plan. Identification of technical difficulties after enrollment, making the studied treatment protocol impossible to implement. Emergent need for treatment due to other diseases confirmed after enrollment. Deviation from the study protocol in the actual administration of treatment. Voluntary withdrawal or discontinuation of any examinations, treatments, and monitoring required by the study at any stage, for personal reasons of the participant.
Sites / Locations
- Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center
Arms of the Study
Arm 1
Experimental
MPD Repair or Reconstruction
In laparoscopic or robotic pancreatic tumor enucleation, it is inevitable that the main pancreatic duct (MPD) may be damaged due to its proximity or encasement by the tumor. After tumor resection, MPD repair or reconstruction can be performed. If there is no associated MPD dilation, a MPD stent can be inserted and secured with interrupted sutures. When placing the stent, it is important to ensure that the distal end of the stent passes through the duodenal papilla to sufficiently reduce the pressure inside the MPD. Vascular remnants or branch pancreatic duct remnants on the pancreatic resection surface should be sutured. After hemostasis, efforts should be made to restore the serosalization of the pancreatic resection surface. The surface can also be left exposed or covered with ligamentum teres hepatis. Fish-mouth-shaped incisions can be closed, but care should be taken to avoid creating dead spaces that may lead to fluid accumulation and hinder drainage.