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High Volume Washing of the Abdomen in Increasing Survival After Surgery in Patients With Pancreatic Cancer That Can Be Removed by Surgery

Primary Purpose

Acinar Cell Carcinoma, Ampulla of Vater Adenocarcinoma, Cholangiocarcinoma

Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Pancreatectomy
Lavage
Pancreatectomy
Lavage
Pancreatectomy
Sponsored by
Sidney Kimmel Cancer Center at Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acinar Cell Carcinoma

Eligibility Criteria

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

Inclusion Criteria:

  • The subject has a surgical indication for pancreatectomy (pancreaticoduodenectomy, distal pancreatectomy, total pancreatectomy)
  • A diagnosis of pancreatic or other periampullary cancer is suspected preoperatively
  • In the opinion of the surgeon, the subject has no medical contraindications to pancreatectomy
  • The subject is willing to consent to randomization of lavage vs. standard lavage

Exclusion Criteria:

  • The subject does not have a surgical indication for pancreatectomy
  • In the opinion of the surgeon, the subject has medical contraindications to pancreatectomy
  • The subject is not willing to consent to EIPL-S lavage vs. EIPL-D lavage vs. standard
  • Subject with neoadjuvant chemotherapy or chemoradiation
  • Known benign or indolent disease, including benign pancreatic cystic tumors or pancreatic endocrine tumors

Sites / Locations

  • Case Western Reserve UniversityRecruiting
  • Sidney Kimmel Cancer Center at Thomas Jefferson UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Sham Comparator

Arm Label

Arm I (EIPL-S)

Arm II (EIPL-D)

ARM III (NO LAVAGE)

Arm Description

Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy. Immediately after removal of tumor, patients receive EIPL-S lavage 10 times over 15 minutes.

Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy. Immediately after removal of tumor, patients receive EIPL-D lavage 10 times over 15 minutes.

Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy with no extensive lavage after removal of tumor.

Outcomes

Primary Outcome Measures

Overall Survival
Will use a one-sided log-rank test to separately compare lavage (EIPL-S or EIPL=D) to no lavage with respect to OS. Assuming the study is not stopped at the interim analyses, the final comparison will be made with an alpha level of 0.02493. Distribution of OS will be estimated using the Kaplan-Meier method. Secondary analyses will use Cox regression to adjust the lavage/no lavage comparison for other baseline patient and/or characteristics known to be associated with OS.

Secondary Outcome Measures

Incidence of overall complications and specific complications graded in severity using Common Terminology Criteria for Adverse Events (v4.0)
Will use chi-square or Fisher's exact test for dichotomous outcomes and Poisson regression for count outcomes.
Disease Free survival
Will use log-rank tests for time-to-event outcomes.
Recurrence free survival rate
Site of first recurrence

Full Information

First Posted
April 29, 2016
Last Updated
July 24, 2023
Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT02757859
Brief Title
High Volume Washing of the Abdomen in Increasing Survival After Surgery in Patients With Pancreatic Cancer That Can Be Removed by Surgery
Official Title
The WASH Trial: A Randomized Trial of Abdominal Lavage Using Distilled Water or Saline at High Volumes for Resected Pancreatic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 27, 2016 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
January 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University
Collaborators
National Cancer Institute (NCI)

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
This randomized clinical trial studies how well high volume washing of the abdomen works in increasing survival after surgery in patients with pancreatic cancer that can be removed by surgery. High volume washings may remove free floating cancers present after surgery and help prolong survival in patients with pancreatic cancer.
Detailed Description
PRIMARY OBJECTIVES: I. Overall survival (OS) (18 to 27 months after resection). SECONDARY OBJECTIVES: I. Disease free survival (DFS). II. Complication rate. III. Site of first-recurrence (by site, and distant vs. local). IV. Clearance of malignant cells pre vs. post-lavage. OUTLINE: Patients are randomized to 1 of 3 arms. ARM I (EIPL-S): Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy. Immediately after removal of tumor, patients receive extensive intraoperative peritoneal saline (EIPL-S) lavage 10 times over 15 minutes. ARM II (EIPL-D): Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy. Immediately after removal of tumor, patients receive extensive intraoperative peritoneal distilled water (EIPL-D) lavage 10 times over 15 minutes. ARM III (NO LAVAGE): Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy with no extensive lavage after removal of tumor. After completion of study treatment, patients are followed up every 3 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acinar Cell Carcinoma, Ampulla of Vater Adenocarcinoma, Cholangiocarcinoma, Duodenal Adenocarcinoma, Pancreatic Adenocarcinoma, Pancreatic Ductal Adenocarcinoma, Pancreatic Intraductal Papillary Mucinous Neoplasm, Periampullary Adenocarcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
845 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm I (EIPL-S)
Arm Type
Active Comparator
Arm Description
Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy. Immediately after removal of tumor, patients receive EIPL-S lavage 10 times over 15 minutes.
Arm Title
Arm II (EIPL-D)
Arm Type
Active Comparator
Arm Description
Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy. Immediately after removal of tumor, patients receive EIPL-D lavage 10 times over 15 minutes.
Arm Title
ARM III (NO LAVAGE)
Arm Type
Sham Comparator
Arm Description
Patients undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy with no extensive lavage after removal of tumor.
Intervention Type
Procedure
Intervention Name(s)
Pancreatectomy
Other Intervention Name(s)
Excision of the Pancreas, Pancreas Excision
Intervention Description
Undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy
Intervention Type
Other
Intervention Name(s)
Lavage
Other Intervention Name(s)
Irrigation, Wash
Intervention Description
Receive EIPL-S
Intervention Type
Procedure
Intervention Name(s)
Pancreatectomy
Other Intervention Name(s)
Excision of the Pancreas, Pancreas Excision
Intervention Description
Undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy
Intervention Type
Other
Intervention Name(s)
Lavage
Other Intervention Name(s)
Irrigation, Wash
Intervention Description
Receive EIPL-D
Intervention Type
Procedure
Intervention Name(s)
Pancreatectomy
Other Intervention Name(s)
Excision of the Pancreas, Pancreas Excision
Intervention Description
Undergo pancreaticoduodenectomy, distal pancreatectomy, or total pancreatectomy
Primary Outcome Measure Information:
Title
Overall Survival
Description
Will use a one-sided log-rank test to separately compare lavage (EIPL-S or EIPL=D) to no lavage with respect to OS. Assuming the study is not stopped at the interim analyses, the final comparison will be made with an alpha level of 0.02493. Distribution of OS will be estimated using the Kaplan-Meier method. Secondary analyses will use Cox regression to adjust the lavage/no lavage comparison for other baseline patient and/or characteristics known to be associated with OS.
Time Frame
Up to 27 months after resection
Secondary Outcome Measure Information:
Title
Incidence of overall complications and specific complications graded in severity using Common Terminology Criteria for Adverse Events (v4.0)
Description
Will use chi-square or Fisher's exact test for dichotomous outcomes and Poisson regression for count outcomes.
Time Frame
Up to 5 years after resection
Title
Disease Free survival
Description
Will use log-rank tests for time-to-event outcomes.
Time Frame
Up to 5 years after resection
Title
Recurrence free survival rate
Time Frame
At 1 year after resection
Title
Site of first recurrence
Time Frame
Up to 5 years after resection
Other Pre-specified Outcome Measures:
Title
Presence of cells in cytologic washing
Description
Will be modeled with repeated measures logistic regression using generalized estimating equations methods. Within this model, group differences in change from post-resection to post-lavage will be compared. McNemar's test for paired dichotomous data will be used to compare presence of cells at pre-dissection to post-resection.
Time Frame
Up to 5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The subject has a surgical indication for pancreatectomy (pancreaticoduodenectomy, distal pancreatectomy, total pancreatectomy) A diagnosis of pancreatic or other periampullary cancer is suspected preoperatively In the opinion of the surgeon, the subject has no medical contraindications to pancreatectomy The subject is willing to consent to randomization of lavage vs. standard lavage Exclusion Criteria: The subject does not have a surgical indication for pancreatectomy In the opinion of the surgeon, the subject has medical contraindications to pancreatectomy Age < 18 years of age The subject is not willing to consent to EIPL-S lavage vs. EIPL-D lavage vs. standard Known benign or indolent disease, including benign pancreatic cystic tumors or pancreatic endocrine tumors Other malignancy within five years, unless the probability of recurrence of the prior malignancy is < 5% as determined by the principal investigator based on available information; patient's curatively treated for squamous and basal cell carcinoma of the skin or patients with a history of malignant tumor in the past that have been disease free for at least five years are also eligible for this study Evidence of metastatic disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Harish Lavu, MD
Phone
215-955-9402
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harish Lavu, MD
Organizational Affiliation
Thomas Jefferson University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jordan Winter, MD
Phone
216-844-5777
Email
jordan.winter@UHhospitals.org
Facility Name
Sidney Kimmel Cancer Center at Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Harish Lavu, MD
Phone
215-955-9402
Email
harish.lavu@jefferson.edu

12. IPD Sharing Statement

Links:
URL
http://hospitals.jefferson.edu/
Description
Thomas Jefferson University Hospital

Learn more about this trial

High Volume Washing of the Abdomen in Increasing Survival After Surgery in Patients With Pancreatic Cancer That Can Be Removed by Surgery

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