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Minimally Invasive Pancreatic Enucleation With Main Pancreatic Duct Repair or Reconstruction

Primary Purpose

Pancreatic Tumor, Benign, Pancreatic Neuroendocrine Tumor, Solid Pseudopapillary Tumor of the Pancreas

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
MPD Repair or Reconstruction
Sponsored by
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Arm Label

MPD Repair or Reconstruction

Arm Description

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.

Outcomes

Primary Outcome Measures

Incidence of Clinically Relevant Postoperative Pancreatic Fistula
Clinically Relevant Pancreatic Fistula including Grade B fistulas, which require treatment beyond simple drainage, as well as Grade C fistulas.

Secondary Outcome Measures

Perioperative complication rate according to the Clavien-Dindo classification
Adverse events that occur during or after the surgery, reported according to the Clavien-Dindo classification.
Postoperative pancreatic hemorrhage (PPH) rate
Postoperative pancreatic hemorrhage (PPH) rate within 90 days after surgery, reported according to the ISGPS definition.
Delayed gastric emptying (DGE) rate
Delayed gastric emptying (DGE) rate within 90 days after surgery, reported according to the ISGPS definition.
Reoperation rate
Reoperation rate within 90 days after surgery.
Rate of pancreatic enzyme-dependent malabsorption
Postoperative pancreatic enzyme-dependent malabsorption rate.
Rate of new-onset diabetes
Postoperative new-onset diabetes rate.
Life quality satisfaction evaluated according to EORTC C30 scale
The patient's health-related quality of life after surgical intervention. It includes physical, emotional, and social aspects of a patient's well-being. This study evaluated quality of life using a telephone survey and the EORTC C30 scales.
R0 resection rate
R0 margin rate on postoperative pathological assessment.
Recurrence-free survival (RFS)
The time of surgery to the time of tumor recurrence or death.

Full Information

First Posted
August 23, 2023
Last Updated
August 29, 2023
Sponsor
Fudan University
Collaborators
The Third Affiliated Hospital of Soochow University, Tongji Hospital, Qilu Hospital of Shandong University, Chinese PLA General Hospital, The Affiliated Hospital of Xuzhou Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT06024343
Brief Title
Minimally Invasive Pancreatic Enucleation With Main Pancreatic Duct Repair or Reconstruction
Official Title
Long-term Prognosis and Quality of Life in Minimally Invasive Pancreatic Enucleation With Main Pancreatic Duct Repair or Reconstruction: A Multicenter Prospective Single-Arm Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
December 31, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University
Collaborators
The Third Affiliated Hospital of Soochow University, Tongji Hospital, Qilu Hospital of Shandong University, Chinese PLA General Hospital, The Affiliated Hospital of Xuzhou Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to evaluate the impact of concomitant main pancreatic duct repair or reconstruction during minimally invasive pancreatic tumor enucleation on long-term patient prognosis and quality of life.
Detailed Description
Standard surgical procedures for benign or low-grade malignant pancreatic tumors is associated with increased risks of postoperative complications and long-term pancreatic functional impairment, while parenchyma-sparing pancreatectomy such as enucleation can reduce the incidence of complications and preserve healthy parenchyma, thereby preserve both endocrine and exocrine pancreatic function. It has been reported that pancreatic tumor enucleation is a safe and feasible approach in preserving normal physiological function in patients undergoing pancreatic surgery. With the growing emphasis on routine screenings and the application of high-quality thin-slice imaging techniques, the detection rates of pancreatic tumors have witnessed a steady increase. Additionally, there is a notable trend towards younger patients being diagnosed with pancreatic tumors. Consequently, in conjunction with ensuring safe and thorough tumor resection while maximizing preservation of pancreatic function, there is a current clinical demand to further reduce surgical trauma. Literature reviews and meta-analyses have demonstrated that minimally invasive enucleation procedures offer well-known advantages associated with minimally invasive approaches, such as shorter postoperative hospital stays and lower overall complication rates. While the occurrence rate of severe complications, such as postoperative hemorrhage, remains relatively low, the development of postoperative pancreatic fistula (POPF) continues to pose a challenging issue. The distance between the tumor and the main pancreatic duct (MPD) is considered a crucial factor influencing the occurrence of POPF after enucleation. However, these data have been rarely described in previous studies, making it challenging to accurately assess their actual impact on the rate of POPF occurrence. Heeger et al. suggested that the risk of POPF increases with closer proximity of the tumor to the MPD. The incidence of POPF was higher in deep-seated tumors after pancreatic enucleation (distance to MPD <3 mm) compared to superficial tumors (>3 mm) (73.3% vs. 30.0%, P=0.002). Other studies have even limited this critical distance to 2mm. Some research has indicated that if the tumor invades or encases the MPD, enucleation surgery should be contraindicated, and standard resection should be preferred to avoid the risk of POPF postoperatively. However, a retrospective analysis by Strobel et al. on 166 cases of pancreatic tumor enucleation demonstrated that even tumors in close proximity to the MPD can be safely resected, although their study did not include cases with tumor encasement of the MPD. In 2021, Professor Liu Rong and colleagues introduced the concept of pancreatic duct surgery and outlined four main surgical approaches: MPD repair, pancreatic end-to-end anastomosis, local excision of branch-duct intraductal papillary mucinous neoplasms, and MPD replacement. However, detailed research data in this field are still lacking. The safety and feasibility of minimally invasive pancreatic tumor enucleation procedures involving MPD repair or reconstruction, the control of POPF, and the long-term prognosis and quality of life of patients after MPD repair or reconstruction remain unclear. Therefore, this study aims to conduct a prospective, multicenter, single-arm clinical trial. The results of this study will serve as a valuable reference for clinical practice and promote the development and application of minimally invasive pancreatic tumor enucleation procedures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Tumor, Benign, Pancreatic Neuroendocrine Tumor, Solid Pseudopapillary Tumor of the Pancreas
Keywords
Pancreatic benign or low-grade malignant tumors, Minimally invasive enucleation, Main Pancreatic Duct Repair or Reconstruction, Long-term prognosis, Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
112 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MPD Repair or Reconstruction
Arm Type
Experimental
Arm Description
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.
Intervention Type
Procedure
Intervention Name(s)
MPD Repair or Reconstruction
Intervention Description
During laparoscopic or robotic pancreatic tumor enucleation, if the main pancreatic duct (MPD) is damaged due to its proximity or encasement by the tumor, MPD repair or reconstruction is performed.
Primary Outcome Measure Information:
Title
Incidence of Clinically Relevant Postoperative Pancreatic Fistula
Description
Clinically Relevant Pancreatic Fistula including Grade B fistulas, which require treatment beyond simple drainage, as well as Grade C fistulas.
Time Frame
Within 90 days after surgery.
Secondary Outcome Measure Information:
Title
Perioperative complication rate according to the Clavien-Dindo classification
Description
Adverse events that occur during or after the surgery, reported according to the Clavien-Dindo classification.
Time Frame
Within 90 days after surgery.
Title
Postoperative pancreatic hemorrhage (PPH) rate
Description
Postoperative pancreatic hemorrhage (PPH) rate within 90 days after surgery, reported according to the ISGPS definition.
Time Frame
Within 90 days after surgery.
Title
Delayed gastric emptying (DGE) rate
Description
Delayed gastric emptying (DGE) rate within 90 days after surgery, reported according to the ISGPS definition.
Time Frame
Within 90 days after surgery.
Title
Reoperation rate
Description
Reoperation rate within 90 days after surgery.
Time Frame
Within 90 days after surgery.
Title
Rate of pancreatic enzyme-dependent malabsorption
Description
Postoperative pancreatic enzyme-dependent malabsorption rate.
Time Frame
Through study completion, an average of 3 year.
Title
Rate of new-onset diabetes
Description
Postoperative new-onset diabetes rate.
Time Frame
Through study completion, an average of 3 year.
Title
Life quality satisfaction evaluated according to EORTC C30 scale
Description
The patient's health-related quality of life after surgical intervention. It includes physical, emotional, and social aspects of a patient's well-being. This study evaluated quality of life using a telephone survey and the EORTC C30 scales.
Time Frame
Through study completion, an average of 3 year.
Title
R0 resection rate
Description
R0 margin rate on postoperative pathological assessment.
Time Frame
From the date of surgery to 1 month after surgery.
Title
Recurrence-free survival (RFS)
Description
The time of surgery to the time of tumor recurrence or death.
Time Frame
Through study completion, an average of 3 year.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xianjun Yu, MD, PhD
Phone
+86-13801669875
Email
yuxianjun@fudanpci.org
First Name & Middle Initial & Last Name or Official Title & Degree
Zheng Li, MD
Phone
+86-18521097686
Email
lizheng@fudanpci.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xianjun Yu, MD, PhD
Organizational Affiliation
Fudan University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xiaowu Xu, MD
Organizational Affiliation
Fudan University
Official's Role
Study Director
Facility Information:
Facility Name
Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center
City
Shanghai
State/Province
Shanghai
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xianjun Yu, MD, PhD
Phone
+86-13801669875
Email
yuxianjun@fudanpci.org
First Name & Middle Initial & Last Name & Degree
Xianjun Yu, MD, PhD
First Name & Middle Initial & Last Name & Degree
Xiaowu Xu, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22528577
Citation
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Links:
URL
https://doi.org/10.1016/j.isurg.2022.11.001
Description
In 2021, Professor Liu Rong and colleagues introduced the concept of pancreatic duct surgery for the first time and outlined four main surgical approaches.

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Minimally Invasive Pancreatic Enucleation With Main Pancreatic Duct Repair or Reconstruction

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