Endoscopic Abraxane Injection Into Pancreatic Cysts
Primary Purpose
Pancreatic Cysts
Status
Terminated
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Albumin bound paclitaxel
Sponsored by
About this trial
This is an interventional treatment trial for Pancreatic Cysts focused on measuring Premalignant, Malignant
Eligibility Criteria
Inclusion Criteria:
- Mucinous cysts (premalignant or malignant cysts of the pancreas)
- Normal organ and marrow function
- Baseline CT within 6 months of enrollment
Exclusion Criteria:
- Pregnant or breastfeeding
- Acute active pancreatitis
- Complicated pancreatic cysts
- Subjects who do not speak English
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Albumin bound paclitaxel
Arm Description
Albumin bound paclitaxel will be administered into the mucinous cyst of pancreas in endoscopy procedure.
Outcomes
Primary Outcome Measures
Frequency of Pancreatitis
Safety of injection of albumin-bound paclitaxel will be measured by the frequency of pancreatitis.
Secondary Outcome Measures
Feasibility of Endoscopic Ultrasonography (EUS) Guided Injection of Albumin-bound Paclitaxel Into Pancreatic Cysts
The feasibility of the procedure will be measured by the ease of injection of albumin-bound paclitaxel into the cyst cavity across the gastro-duodenal wall. On a subjective scale, the endoscopist will note the ease of the procedure on a scale of 0-5, with 5 being very easy and 0 is not possible. Any score less than 2 will be considered unacceptable and failure of the study.
Size of Cystic Lesion
Determine the size of the cystic lesion using CT scanning. Number of participants with reduction in size, persistent size, or increase in size of cyst are reported.
Full Information
NCT ID
NCT01698710
First Posted
October 1, 2012
Last Updated
May 26, 2017
Sponsor
Massachusetts General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01698710
Brief Title
Endoscopic Abraxane Injection Into Pancreatic Cysts
Official Title
EUS Guided Injection of Albumin Bound Paclitaxel Into Pancreatic Cysts
Study Type
Interventional
2. Study Status
Record Verification Date
September 2014
Overall Recruitment Status
Terminated
Why Stopped
expiration of IRB approval
Study Start Date
November 2012 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
September 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This research study is a pilot study. In this pilot study we are testing the safety of a procedure. "Investigational" means that the Albumin bound paclitaxel (Abraxane) is still being studied and that research doctors are trying to find out more about it. It also means that the FDA has not approved Abraxane injection for your type of medical condition. Treatment of pancreatic cysts often requires follow-up imaging studies and surgical resection of the cysts. As part of standard medical care, you will be undergoing a diagnostic endoscopic ultrasound guided fine needle aspiration (EUS-FNA) in order to evaluate type of the cyst. During the EUS and just after the cyst fluid aspiration, you will undergo the injection of the drug into the cyst cavity if your cyst is thought to be cancerous or precancerous. Cyst fluid will be analyzed for further diagnosis.
Detailed Description
You will be asked to undergo some screening tests or procedures to find out if you can be in the research study. Many of these tests and procedures are likely to be part of regular cancer care and may be done even if it turns out that you do not take part in the research study. If you have had some of these tests or procedures recently, they may or may not have to be repeated. Screening tests include the following: medical history, performance status, assessment of pancreatic cyst by CT, MRI or EUS, blood tests and a pregnancy test.
If these tests show that you are eligible to participate in the research study, you will begin the study treatment. If you do not meet the eligibility criteria you will not be able to participate in this research study.
As part of your medical care you will be undergoing an endoscopic procedure EUS-FNA (Endoscopic Ultrasound Fine Needle Aspiration) in order to evaluate and evacuate the cyst fluid. During the EUS-FNA and just after the cyst fluid aspiration, albumin bound paclitaxel will be injected into the cyst cavity.
The study procedure (injection of drug into cyst cavity) takes place over 5 minutes during the EUS-FNA. 2 days after the procedure you will receive a phone call from the research coordinator to check on how you are feeling. 3 months after study procedure participants will undergo a follow up CT to see what happened to the cyst. You will continue to have routine follow up for your medical problems.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cysts
Keywords
Premalignant, Malignant
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Albumin bound paclitaxel
Arm Type
Experimental
Arm Description
Albumin bound paclitaxel will be administered into the mucinous cyst of pancreas in endoscopy procedure.
Intervention Type
Drug
Intervention Name(s)
Albumin bound paclitaxel
Other Intervention Name(s)
Abraxane
Intervention Description
Albumin bound paclitaxel will be administered into the mucinous cyst of pancreas in endoscopy procedure.
Primary Outcome Measure Information:
Title
Frequency of Pancreatitis
Description
Safety of injection of albumin-bound paclitaxel will be measured by the frequency of pancreatitis.
Time Frame
3-10 months (median 6 months) after injection therapy
Secondary Outcome Measure Information:
Title
Feasibility of Endoscopic Ultrasonography (EUS) Guided Injection of Albumin-bound Paclitaxel Into Pancreatic Cysts
Description
The feasibility of the procedure will be measured by the ease of injection of albumin-bound paclitaxel into the cyst cavity across the gastro-duodenal wall. On a subjective scale, the endoscopist will note the ease of the procedure on a scale of 0-5, with 5 being very easy and 0 is not possible. Any score less than 2 will be considered unacceptable and failure of the study.
Time Frame
immediately after procedure
Title
Size of Cystic Lesion
Description
Determine the size of the cystic lesion using CT scanning. Number of participants with reduction in size, persistent size, or increase in size of cyst are reported.
Time Frame
3-10 months (median 6 months) after injection therapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Mucinous cysts (premalignant or malignant cysts of the pancreas)
Normal organ and marrow function
Baseline CT within 6 months of enrollment
Exclusion Criteria:
Pregnant or breastfeeding
Acute active pancreatitis
Complicated pancreatic cysts
Subjects who do not speak English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William Brugge, MD
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Endoscopic Abraxane Injection Into Pancreatic Cysts
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