search
Back to results

A Prospective Randomized Multi-center Study for Efficacy of Metallic Biliary Stent Compared to Plastic Stent in Patients Receiving Neoadjuvant Chemotherapy for Resectable Pancreatic Cancer

Primary Purpose

Resectable Pancreatic Cancer With Biliary Obstruction

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
ERCP using plastic stent
ERCP using metal stent
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Resectable Pancreatic Cancer With Biliary Obstruction

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients aged 20 years or older who have confirmed histologically or radiologically resectable pancreatic cancer
  2. Patients with clinical obstruction symptoms and radiographically confirmed biliary obstruction related to malignant tumors
  3. Patients receiving neoadjuvant chemotherapy before surgery

Exclusion Criteria:

  1. Patients diagnosed as unresectable pancreatic cancer
  2. Patients with biliary obstruction due to biliary cancer, not pancreatic cancer
  3. Patients with duodenal obstruction
  4. Patients with pancreatic cance and other cancers
  5. Patients with severe uncontrolled infection
  6. Patients with 3 or higher of performance score as the Eastern Cooperative Oncology Group
  7. Patients who have not agreed with the informed consent
  8. Patients who are technically unable to be undergone endoscopic procedures

Sites / Locations

  • Severance Hospital, Yonsei University Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

The Plastic stent

The metal stent

Arm Description

Patient group with plastic stent inserted in biliary obstruction through endoscope

Patient group with metal stent inserted in biliary obstruction through endoscope

Outcomes

Primary Outcome Measures

Re-intervention rate
Re-intervention because of obstructive jaundice, cholangitis, stent malfunction, complication of procedure of ERCP

Secondary Outcome Measures

Procedure related complication, Postoperative complication
Complication because of procedure (ERCP) Complication because of surgery

Full Information

First Posted
May 28, 2021
Last Updated
May 28, 2021
Sponsor
Yonsei University
search

1. Study Identification

Unique Protocol Identification Number
NCT04911647
Brief Title
A Prospective Randomized Multi-center Study for Efficacy of Metallic Biliary Stent Compared to Plastic Stent in Patients Receiving Neoadjuvant Chemotherapy for Resectable Pancreatic Cancer
Official Title
A Prospective Randomized Multi-center Study for Efficacy of Metallic Biliary Stent Compared to Plastic Stent in Patients Receiving Neoadjuvant Chemotherapy for Resectable Pancreatic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 2021 (Anticipated)
Primary Completion Date
June 2022 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei 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
Pancreatic cancer is the eighth most common occurrence in Korea. In the United States, pancreatic cancer is expected to be the number two cause of death from cancer in 2030. The prevalence of pancreatic cancer is also on the rise in Korea. The 5-year survival rate of pancreatic cancer in Korea is 10.8%. According to the 2017 cause of death statistics, pancreatic cancer mortality is ranked fifth. It is known to have the worst prognosis of cancer in the body. The median survival period of unresectable pancreatic cancer is only six months, and resection is the only treatment that can be expected to be completely cured, but only about 10% of cases are possible to be operable at the time of diagnosis. In the 2000s, the studies began to emerge on diagnosis and treatment of pancreatic cancer with intermediate anatomical and imaging characteristics of resectable and locally advanced pancreatic cancer. Margin negative resection plays an important role in the long-term survival rate in surgical treatment of pancreatic cancer. Prior to 2001, pancreatic cancer with invasion of vein was considered impossible to perform radical resection. However, the studies have been published that a satisfactory long-term survival rate and margin negative resection could be obtained when venous resection was performed along with radical resection. Since the 2006, the National Comprehensive Cancer Network (NCCN) guideline, after performing radical resection among locally advanced pancreatic cancers without remote metastasis, pancreatic cancers with high risk of margin positive resection and treatment failure were classified as "borderline resectable". In the borderline resectable pancreatic cancer, neoadjuvant therapy was recommended before surgery. In recent years, the neoadjuvant therapy has been reported to raise the survival rate in resectable pancreatic cancer. Furthermore, a prospective study is in progress to demonstrate the effectiveness of neoadjuvant therapy with FOLFIRINOX in resectable pancreatic cancer. If pancreatic cancer is located in the head of pancreas, jaundice can be occurred often. In the case of preoperative jaundice, the possibility of postoperative complications increases. So biliary drainage is performed before surgery. In biliary drainage, usually the plastic stent was inserted through the endoscope. If the metal stent is inserted in the biliary obstruction, it can cause severe inflammation around the bile duct due to the radial force, and it is difficult to remove in the surgery. However, the meta-analysis comparing the groups of metal and plastic stents in the recent preoperative biliary drainage showed no difference of postoperative complication, and postoperative pancreatic fistula was lower in the group of metal stents (5.1% vs. 11.8% p=0.04). In addition, fewer re-intervention cases before surgery were found in the group of metal stents (3.4% vs.14.8% p < 0.0001). Not only in the borderline resectable, but also in the resectable pancreatic cancer, neoadjuvant therapy has recently been actively performed in the cases of large tumor size, high CA 19-9, large lymph nodes, severe weight loss, and severe pain. The comparison study of the efficacy between plastic and metal stents in preoperative bile drainage in pancreatic cancer with neoadjuvant therapy has not yet been prospectively performed. However, retrospective studies have shown that metal stents have a lower re-treatment rate than plastic stent (0.24 vs 0.54), and that there is no difference in post-operative complications. Therefore, we planned the study to compare the efficacy and safety between metal and plastic stent in biliary drainage performed in patients undergoing neoadjuvant therapy with pancreatic cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Resectable Pancreatic Cancer With Biliary Obstruction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
196 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
The Plastic stent
Arm Type
Active Comparator
Arm Description
Patient group with plastic stent inserted in biliary obstruction through endoscope
Arm Title
The metal stent
Arm Type
Experimental
Arm Description
Patient group with metal stent inserted in biliary obstruction through endoscope
Intervention Type
Device
Intervention Name(s)
ERCP using plastic stent
Intervention Description
Insertion of plastic stent (plastic stent with inner diameter 1.8mm or more) in the biliary obstruction will be performed using ERCP in the patients with the pancreatic cancer undergoing neoadjuvant therapy.
Intervention Type
Device
Intervention Name(s)
ERCP using metal stent
Intervention Description
Insertion of metal stent (full covered self-expandable metal stent) in the biliary obstruction will be performed using ERCP in the patients with the pancreatic cancer undergoing neoadjuvant therapy.
Primary Outcome Measure Information:
Title
Re-intervention rate
Description
Re-intervention because of obstructive jaundice, cholangitis, stent malfunction, complication of procedure of ERCP
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Procedure related complication, Postoperative complication
Description
Complication because of procedure (ERCP) Complication because of surgery
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 20 years or older who have confirmed histologically or radiologically resectable pancreatic cancer Patients with clinical obstruction symptoms and radiographically confirmed biliary obstruction related to malignant tumors Patients receiving neoadjuvant chemotherapy before surgery Exclusion Criteria: Patients diagnosed as unresectable pancreatic cancer Patients with biliary obstruction due to biliary cancer, not pancreatic cancer Patients with duodenal obstruction Patients with pancreatic cance and other cancers Patients with severe uncontrolled infection Patients with 3 or higher of performance score as the Eastern Cooperative Oncology Group Patients who have not agreed with the informed consent Patients who are technically unable to be undergone endoscopic procedures
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Seung Min Bang
Phone
82-2-2228-1995
Email
bang7028@yuhs.ac
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Seung Min Bang
Organizational Affiliation
Severance Hospital, Yonsei University Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Severance Hospital, Yonsei University Health System
City
Seoul
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Seung Min Bang
Phone
82-2-2228-1995
Email
bang7028@yuhs.ac

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Prospective Randomized Multi-center Study for Efficacy of Metallic Biliary Stent Compared to Plastic Stent in Patients Receiving Neoadjuvant Chemotherapy for Resectable Pancreatic Cancer

We'll reach out to this number within 24 hrs