Pilot and Feasibility Study of the Imaging Potential of EC17: Intraoperative Folate-fluorescein Conjugate (EC17) Lung Cancer (CA)
Primary Purpose
Lung and Pleural Malignancies, Neoplasms, Nodules
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
EC17 imaging contrast agent
Sponsored by
About this trial
This is an interventional diagnostic trial for Lung and Pleural Malignancies
Eligibility Criteria
Inclusion Criteria:
- Adult patients over 18 years of age
- Patients presenting with a lung or pleural nodule or mass presumed to be resectable on pre-operative assessment
- Good operative candidate
- Subject capable of giving informed consent and participating in the process of consent
Exclusion Criteria:
- Pregnant women as determined by urinary or serum beta human chorionic gonadotropin (hCG) within 72 hours of surgery
- Patients with a history of anaphylactic reactions to Folate-FITC or insects
At-risk patient populations:
- Homeless patients
- Patients with drug or alcohol dependence
- Children and neonates
- Patients unable to participate in the consent process
Sites / Locations
- Hospital of the University of Pennsylvania
- Philadelphia VA Medical Center, Philadelphia, PA
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
IV Injection of EC17
Arm Description
The group will receive a single dose of EC17, infused over 10 minutes, prior to surgery. Then, during surgery, the EC-17 will be imaged with a camera that the investigators have developed.
Outcomes
Primary Outcome Measures
Number of FRA tumors identified by EC17 during surgery.
Measure the number of patients who have a positive margin during lung cancer surgery 2 - 4 hours after receiving administration of EC17.
Secondary Outcome Measures
The number of participants that will have an adverse reaction to the EC17
Full Information
NCT ID
NCT01778920
First Posted
January 18, 2013
Last Updated
May 16, 2016
Sponsor
University of Pennsylvania
Collaborators
VA Office of Research and Development
1. Study Identification
Unique Protocol Identification Number
NCT01778920
Brief Title
Pilot and Feasibility Study of the Imaging Potential of EC17: Intraoperative Folate-fluorescein Conjugate (EC17) Lung Cancer (CA)
Official Title
Intraoperative Imaging of Pulmonary Adenocarcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
April 2012 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
May 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Pennsylvania
Collaborators
VA Office of Research and Development
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The goal of this study is to perform imaging of patient's tumors while the chest is open and the tumor is being removed.
According to the World Health Organization, lung cancer is the most common cause of cancer-related death in men and women, and is responsible for 1.3 million deaths worldwide annually as of 2004. Surgery remains the best option for patients presenting with operable Stage I or II cancers, however the five year survival rate for these candidates remains at a dismal 53% for Stage I and 32% for Stage II. The high rates of recurrence suggest that surgeons are unable to completely detect and remove primary tumor nodules in a satisfactory manner as well as lingering metastases in sentinel lymph nodes. By ensuring a negative margin through imaging during surgery it would be possible for us to improve the rates of recurrence free patients and thus overall survival.
Thoracic malignancies are the ideal disease to investigate intra-operative imaging. Over 85% of lung and pleural malignancies express folate receptor alpha (FRA). It is important to note that FRA is expressed only in the proximal tubules of the kidneys, activated macrophages, and in the choroidal plexus. Thus, the false positive detection rate is expected to be extremely low. A group well known to us in the Netherlands has completed a pilot study utilizing a folate-fluorescein isothiocyanate (folate-FITC) conjugate in 12 patients with ovarian cancer. Another group of investigators in Mayo have subsequently performed this study on 20 more patients without any serious adverse events (personal communication). They report excellent sensitivity and specificity with this technique with only grade 1 side effects (allergic reaction). All side effects reversed when the injection was halted. Patients with a history of allergic reactions to insect bites should not participate (fluorescein is derived from the firefly insect, folate is an essential vitamin).
Detailed Description
This will identify the margins and the lymph nodes that may have cancer cells during cancer surgery
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung and Pleural Malignancies, Neoplasms, Nodules, Adenocarcinoma
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
48 (Actual)
8. Arms, Groups, and Interventions
Arm Title
IV Injection of EC17
Arm Type
Experimental
Arm Description
The group will receive a single dose of EC17, infused over 10 minutes, prior to surgery. Then, during surgery, the EC-17 will be imaged with a camera that the investigators have developed.
Intervention Type
Drug
Intervention Name(s)
EC17 imaging contrast agent
Intervention Description
This is an imaging agent to locate lung adenocarcinoma cancer cells during surgery
Primary Outcome Measure Information:
Title
Number of FRA tumors identified by EC17 during surgery.
Description
Measure the number of patients who have a positive margin during lung cancer surgery 2 - 4 hours after receiving administration of EC17.
Time Frame
Within two to four hours of injection of the EC17
Secondary Outcome Measure Information:
Title
The number of participants that will have an adverse reaction to the EC17
Time Frame
Day 1 - Day 30
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients over 18 years of age
Patients presenting with a lung or pleural nodule or mass presumed to be resectable on pre-operative assessment
Good operative candidate
Subject capable of giving informed consent and participating in the process of consent
Exclusion Criteria:
Pregnant women as determined by urinary or serum beta human chorionic gonadotropin (hCG) within 72 hours of surgery
Patients with a history of anaphylactic reactions to Folate-FITC or insects
At-risk patient populations:
Homeless patients
Patients with drug or alcohol dependence
Children and neonates
Patients unable to participate in the consent process
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sunil Singhal, MD
Organizational Affiliation
Philadelphia VA Medical Center, Philadelphia, PA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Philadelphia VA Medical Center, Philadelphia, PA
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26126457
Citation
Okusanya OT, DeJesus EM, Jiang JX, Judy RP, Venegas OG, Deshpande CG, Heitjan DF, Nie S, Low PS, Singhal S. Intraoperative molecular imaging can identify lung adenocarcinomas during pulmonary resection. J Thorac Cardiovasc Surg. 2015 Jul;150(1):28-35.e1. doi: 10.1016/j.jtcvs.2015.05.014. Epub 2015 May 7.
Results Reference
result
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Pilot and Feasibility Study of the Imaging Potential of EC17: Intraoperative Folate-fluorescein Conjugate (EC17) Lung Cancer (CA)
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