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Endoscopic Ultrasound and Endoscopic Retrograde Cholangiopancreatography for Malignant Distal Biliary Obstruction

Primary Purpose

Pancreatic Cancer, Pancreatic Neoplasms, Pancreatic Adenocarcinoma

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EUS-BD
ERCP
Sponsored by
AdventHealth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. ≥ 18 years of age.
  2. Has jaundice due to malignant distal (more than 3cm distal to liver hilum) biliary obstruction.
  3. The subject (or when applicable the subject's LAR) is able to understand and willing to sign an informed consent form prior to the initiation of any study procedures.

Exclusion Criteria:

  1. Age <18 years
  2. Females who are pregnant or lactating. Pregnancy in females of childbearing potential will be determined by routine preoperative urine HCG testing.
  3. Coagulopathy which cannot be corrected (INR >1.6, thrombocytopenia with platelet count <50,000/ml)
  4. Has surgically altered gastrointestinal anatomy such as but not limited to (Billroth II/Roux en-Y, gastric bypass).
  5. Liver metastasis involving >30% of liver volume.
  6. Liver cirrhosis with portal hypertension and/or ascites.

Sites / Locations

  • Center for Interventional Endoscopy - Florida Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

EUS-BD

ERCP

Arm Description

EUS-BD is a minimally invasive technique where the common bile duct (choledochoduodenostomy) is punctured under EUS-guidance and after transmural dilation, a stent is deployed for biliary drainage.

At ERCP, the common bile duct will be selectively cannulated using a sphincterotome and guide wire technique. Once biliary access is obtained a stent will be deployed to facilitate biliary drainage.

Outcomes

Primary Outcome Measures

Rates of perforation
As defined by evidence of air or luminal contents outside the GI tract
Rates of pancreatitis
Defined as typical pain with amylase/lipase >3 times normal
Rates of bile leak
Not caused by pancreatitis or perforation
Rates of bleeding
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Rates of infection (cholangitis)
As defined by >38C >24 hours with cholestasis
Rates of peritionitis
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Rates of cholecystitis
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Rates of pneumoperitoneum
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Rates of fever
Defined as temperature >38C
Rates of abdominal pain
Defined as pain described by the patient not caused by pancreatitis or perforation
Rates of death attributable to the procedure.
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503

Secondary Outcome Measures

Technical Success
Defined as successful placement of a stent for malignant distal biliary obstruction in the desired location as determined at ERCP and EUS in the index session.
Treatment success
Clinical success is defined as decrease in direct bilirubin by 50% at 2 weeks
Procedural duration
Defined as the time between procedure onset and completion of the procedure (stent deployment). The duration will be calculated in minutes from the time the echoendoscope or duodenoscope is positioned and the stent is deployed.
Reintervention
Need for additional intervention (endoscopic, surgical or radiological) to relieve jaundice in the presence of dilated biliary system

Full Information

First Posted
January 17, 2017
Last Updated
February 12, 2019
Sponsor
AdventHealth
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1. Study Identification

Unique Protocol Identification Number
NCT03054987
Brief Title
Endoscopic Ultrasound and Endoscopic Retrograde Cholangiopancreatography for Malignant Distal Biliary Obstruction
Official Title
Randomized Trial Comparing Endoscopic Ultrasound-guided Biliary Drainage (EUS-BD) and Endoscopic Retrograde Cholangiopancreatography (ERCP) for Malignant Distal Biliary Obstruction
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
September 2016 (Actual)
Primary Completion Date
September 2018 (Actual)
Study Completion Date
October 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AdventHealth

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the rates of adverse events between patients undergoing Endoscopic Ultrasound- guided biliary drainage and Endoscopic Retrograde Cholangiopancreatography for distal malignant biliary obstruction.
Detailed Description
The current curative treatment for patients with occlusion of the distal common bile duct by pancreatic cancer is pancreaticoduodenectomy (Whipple procedure). Unfortunately, more than 80% of patients have locally advanced or metastatic disease that requires neoadjuvant or palliative treatment. The goals of biliary drainage in the setting of locally advanced or metastatic pancreatic cancer are to palliate obstructive jaundice and lower serum bilirubin prior to systemic chemotherapy. In addition to resolving jaundice and associated pruritus, biliary drainage improves anorexia, indigestion and quality of life (1, 2). Endoscopic approach by means of retrograde cholangiopancreatography (ERCP) and biliary stent placement is the preferred treatment option for palliation of malignant obstructive jaundice. Endoscopic biliary drainage is safer than surgical bypass, with endoscopic placement of a plastic or metal stent having a lower relative risk of complications (3). When performed by experts, ERCP has favorable (80-90%) short-term (<90 days) success rates in the setting of malignant distal biliary obstruction (1-3). The rate of ERCP-associated adverse events (AEs) is 5-27% (4-7) and include pancreatitis, bleeding, infection, perforation and rarely death. In a recent audit of 524 consecutive patients with an intact papilla who underwent ERCP at a tertiary endoscopy unit, 49 (9.4%) had a previously failed attempt at an outside facility and more than 80% of these failures were in the setting of a distal malignant stricture (8). Cancer in the pancreatic head or uncinate process can cause extensive ampullary inflammation that precludes successful biliary cannulation using standard techniques. In such circumstances, advanced techniques such as needle-knife sphincterotomy, dual wire technique, trans-papillary pancreatic sphincterotomy and cannulation over a pancreatic duct stent are performed to access the bile duct (9, 10). While the technical success rate for advanced techniques in expert hands is more than 85%, the procedure is associated with an AE rate of about 10-20% (9-11). When ERCP is technically unsuccessful, patients are usually referred for interventional radiology-guided percutaneous transhepatic biliary drainage (PTBD). PTBD is usually a multi-step procedure that involves the initial placement of an external drainage catheter followed by internal trans-papillary stent placement. When the distal bile duct is severely strictured or when the intra-hepatic biliary system is non-dilated, PTBD is unsuccessful and is encountered in about 5-15% of patients with pancreatic cancer (12). The rate of short and long-term PTBD-related AEs is 5-10% and 20-30%, respectively (12-14). While most short-term AEs are due to infection and bleeding, the long-term AEs are due to stent dysfunction requiring frequent readmissions (12-14). More recently, EUS-guided biliary drainage (EUS-BD) has emerged as a novel alternative to PTBD and ERCP for biliary decompression when advanced cannulation techniques fail. EUS-BD is a minimally invasive technique where the extra-hepatic common bile duct (choledochoduodenostomy) or intrahepatic bile duct (hepatogastrostomy) is punctured under EUS-guidance and after transmural dilation a stent is deployed for biliary drainage. The potential advantages of EUS-BD are three-fold. Firstly, EUS-BD can be performed from multiple routes in the stomach and duodenum. Thus, duodenal stenosis is not a limitation to biliary access. Secondly, as biliary access is gained distant from the major duodenal papilla, the risk of post-procedure pancreatitis is low. Thirdly, as the deployed stent does not traverse the tumor, its patency could be longer. In a recent study of 95 patients with failed ERCP or inaccessible papilla, direct EUS-guided biliary drainage was successful in 86% of patients with an AE rate of 10.5% that included pancreatitis, bleeding, perforation, bile leak and infection (15). Most AEs were managed conservatively without the need for aggressive treatment measures. In another small, randomized trial of 25 patients with inoperable malignant biliary obstruction, there was no difference in clinical success, AEs, and costs between patients randomized to EUS-BD or PTBD (16). In a recent retrospective study of 208 patients with malignant obstructive jaundice treated by ERCP or EUS-BD directed biliary metal stent placement, there was no difference in the rates of technical success (>90% in both cohorts) or AEs (8.65% in both cohorts) between groups (17). However, patients who underwent ERCP had a 5% incidence of post-procedure pancreatitis compared to 0% in the EUS-BD cohort. Given these promising outcomes, EUS-BD is currently practiced as a complimentary therapy that allows biliary drainage when technical failure is encountered at ERCP. EUS-BD and PTBD have been shown to be comparable in effectiveness after failed ERCP, however patients who underwent PTBD had higher rates of adverse events and required additional interventions (19). PTBD and EUS-BD have shown to be equally effective treatment options (16). The effectiveness of treatment outcomes between EUS-BD and ERCP needs to be evaluated. Since the treatment outcomes and safety profile of EUS-BD is comparable to ERCP and because EUS-BD is successful in more than 85% of patients with a failed ERCP, EUS-BD could be a first-line treatment option and not just a rescue measure for patients with malignant distal biliary obstruction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer, Pancreatic Neoplasms, Pancreatic Adenocarcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
67 (Actual)

8. Arms, Groups, and Interventions

Arm Title
EUS-BD
Arm Type
Active Comparator
Arm Description
EUS-BD is a minimally invasive technique where the common bile duct (choledochoduodenostomy) is punctured under EUS-guidance and after transmural dilation, a stent is deployed for biliary drainage.
Arm Title
ERCP
Arm Type
Active Comparator
Arm Description
At ERCP, the common bile duct will be selectively cannulated using a sphincterotome and guide wire technique. Once biliary access is obtained a stent will be deployed to facilitate biliary drainage.
Intervention Type
Procedure
Intervention Name(s)
EUS-BD
Other Intervention Name(s)
Endoscopic Ultrasound-guided biliary drainage
Intervention Description
EUS-BD is a minimally invasive technique where the common bile duct (choledochoduodenostomy) is punctured under EUS-guidance and after transmural dilation, a stent is deployed for biliary drainage.
Intervention Type
Procedure
Intervention Name(s)
ERCP
Other Intervention Name(s)
Endoscopic Retrograde Cholangiopancreatography
Intervention Description
During the ERCP, a small catheter and guidewire is inserted into the bile duct and the stent can be deployed into the duct.
Primary Outcome Measure Information:
Title
Rates of perforation
Description
As defined by evidence of air or luminal contents outside the GI tract
Time Frame
1 week
Title
Rates of pancreatitis
Description
Defined as typical pain with amylase/lipase >3 times normal
Time Frame
1 week
Title
Rates of bile leak
Description
Not caused by pancreatitis or perforation
Time Frame
1 week
Title
Rates of bleeding
Description
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Time Frame
1 week
Title
Rates of infection (cholangitis)
Description
As defined by >38C >24 hours with cholestasis
Time Frame
1 week
Title
Rates of peritionitis
Description
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Time Frame
1 week
Title
Rates of cholecystitis
Description
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Time Frame
1 week
Title
Rates of pneumoperitoneum
Description
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Time Frame
1 week
Title
Rates of fever
Description
Defined as temperature >38C
Time Frame
1 week
Title
Rates of abdominal pain
Description
Defined as pain described by the patient not caused by pancreatitis or perforation
Time Frame
1 week
Title
Rates of death attributable to the procedure.
Description
As defined by "A lexicon for endoscopic adverse events: report of an ASGE workshop" PMID: 20189503
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Technical Success
Description
Defined as successful placement of a stent for malignant distal biliary obstruction in the desired location as determined at ERCP and EUS in the index session.
Time Frame
1 day
Title
Treatment success
Description
Clinical success is defined as decrease in direct bilirubin by 50% at 2 weeks
Time Frame
2 weeks
Title
Procedural duration
Description
Defined as the time between procedure onset and completion of the procedure (stent deployment). The duration will be calculated in minutes from the time the echoendoscope or duodenoscope is positioned and the stent is deployed.
Time Frame
1 day
Title
Reintervention
Description
Need for additional intervention (endoscopic, surgical or radiological) to relieve jaundice in the presence of dilated biliary system
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: ≥ 18 years of age. Has jaundice due to malignant distal (more than 3cm distal to liver hilum) biliary obstruction. The subject (or when applicable the subject's LAR) is able to understand and willing to sign an informed consent form prior to the initiation of any study procedures. Exclusion Criteria: Age <18 years Females who are pregnant or lactating. Pregnancy in females of childbearing potential will be determined by routine preoperative urine HCG testing. Coagulopathy which cannot be corrected (INR >1.6, thrombocytopenia with platelet count <50,000/ml) Has surgically altered gastrointestinal anatomy such as but not limited to (Billroth II/Roux en-Y, gastric bypass). Liver metastasis involving >30% of liver volume. Liver cirrhosis with portal hypertension and/or ascites.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shyam Varadarajulu, MD
Organizational Affiliation
AdventHealth
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Interventional Endoscopy - Florida Hospital
City
Orlando
State/Province
Florida
ZIP/Postal Code
32803
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The data will be shared via publication and/or presentation.
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Endoscopic Ultrasound and Endoscopic Retrograde Cholangiopancreatography for Malignant Distal Biliary Obstruction

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