IRDye800CW-BBN PET-NIRF Imaging Guiding Surgery in Patients With Glioblastoma
Primary Purpose
Glioblastoma
Status
Unknown status
Phase
Early Phase 1
Locations
China
Study Type
Interventional
Intervention
68Ga-BBN-IRDye800CW
PET/NIRF
PET/NIR fluorescent imaging-guided surgery
Sponsored by
About this trial
This is an interventional diagnostic trial for Glioblastoma focused on measuring GBM, GRPR, IRDye800, NIRF, surgery
Eligibility Criteria
Inclusion Criteria:
- Must be able to provide a written informed consent
- MRI imaging and/or pathological evidence of Newly Diagnosed or recurrence GBM
Exclusion Criteria:
- Consisted of conditions of mental illness
- Severe liver or kidney disease with serum creatinine > 3.0 mg/dl (270 μΜ)
- Any hepatic enzyme level 5 times or more than normal upper limit
- Severe allergy or hypersensitivity to IV radiographic contrast
- Claustrophobia to accept the PET/CT scanning
- Pregnancy or breast feeding
Sites / Locations
- Beijing Tiantan Hospital, Capital Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
68Ga-BBN-IRDye800CW PET/NIRF
Arm Description
The patients were injected with 40μg/111-148 Mega-Becquerel (MBq) 68Ga-BBN-IRDye800CW in one dose intravenously and then underwent PET scan 30 min later before the operation and intraoperative 1.0 mg/ml BBN-IRDye800CW injected intravenously for near-infrared (NIR) fluorescent imaging-guided surgery.
Outcomes
Primary Outcome Measures
Standardized uptake value of 68Ga-BBN-IRDye800CW in PET imaging of GBM
The semiquantitative analysis will be performed by the same person for all the cases, and the standardized uptake value (SUV) of the tracer in GBM will be measured.
Margin assessment of positive tumors in NIRF fluorescent-guided surgery
Secondary Outcome Measures
Full Information
NCT ID
NCT02910804
First Posted
September 16, 2016
Last Updated
January 16, 2018
Sponsor
Beijing Tiantan Hospital
Collaborators
Peking Union Medical College Hospital, National Institute for Biomedical Imaging and Bioengineering (NIBIB), Chinese Academy of Sciences
1. Study Identification
Unique Protocol Identification Number
NCT02910804
Brief Title
IRDye800CW-BBN PET-NIRF Imaging Guiding Surgery in Patients With Glioblastoma
Official Title
PET-NIRF Dual Modality Imaging Guiding Surgery in Patients With Glioblastoma
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 2015 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing Tiantan Hospital
Collaborators
Peking Union Medical College Hospital, National Institute for Biomedical Imaging and Bioengineering (NIBIB), Chinese Academy of Sciences
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is an open-label positron emission tomography/near infrared (PET/NIRF) study to investigate the imaging navigation performance and evaluation efficacy of dual modality imaging probe 68Ga-BBN-IRDye800CW in glioblastoma (GBM) patients. A single dose of 40μg/111-148 Mega-Becquerel (MBq) and 1.0 mg/ml 68Ga-BBN-IRDye800CW will be injected intravenously before the operation and intraoperative respectively. Visual and semiquantitative method will be used to assess the PET images and real-time margins localization for surgical navigation.
Detailed Description
Non-invasive preoperative PET imaging evaluation and real-time fluorescence-guided surgery would be of great help in GBM patients. BBN, with the amino acid sequence of Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2, has been extensively used for the development of molecular probes for the imaging of gastrin-releasing peptide receptor (GRPR), a member of the G protein-coupled receptor family of bombesin receptors that over-expressed in various types of cancer cells including glioblastoma multiforme. For interests in clinical translation of GRPR targeting dual modality probe, an open label dual modality imaging PET/ NIFR study was designed to investigate the safety and imaging guiding performance of 68Ga-BBN-IRDye800CW in patients with GBM.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma
Keywords
GBM, GRPR, IRDye800, NIRF, surgery
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
68Ga-BBN-IRDye800CW PET/NIRF
Arm Type
Experimental
Arm Description
The patients were injected with 40μg/111-148 Mega-Becquerel (MBq) 68Ga-BBN-IRDye800CW in one dose intravenously and then underwent PET scan 30 min later before the operation and intraoperative 1.0 mg/ml BBN-IRDye800CW injected intravenously for near-infrared (NIR) fluorescent imaging-guided surgery.
Intervention Type
Drug
Intervention Name(s)
68Ga-BBN-IRDye800CW
Other Intervention Name(s)
BBN-IRDye800CW
Intervention Type
Device
Intervention Name(s)
PET/NIRF
Other Intervention Name(s)
Positron emission tomography/Near-infrared fluorescent
Intervention Type
Procedure
Intervention Name(s)
PET/NIR fluorescent imaging-guided surgery
Primary Outcome Measure Information:
Title
Standardized uptake value of 68Ga-BBN-IRDye800CW in PET imaging of GBM
Description
The semiquantitative analysis will be performed by the same person for all the cases, and the standardized uptake value (SUV) of the tracer in GBM will be measured.
Time Frame
1 year
Title
Margin assessment of positive tumors in NIRF fluorescent-guided surgery
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Must be able to provide a written informed consent
MRI imaging and/or pathological evidence of Newly Diagnosed or recurrence GBM
Exclusion Criteria:
Consisted of conditions of mental illness
Severe liver or kidney disease with serum creatinine > 3.0 mg/dl (270 μΜ)
Any hepatic enzyme level 5 times or more than normal upper limit
Severe allergy or hypersensitivity to IV radiographic contrast
Claustrophobia to accept the PET/CT scanning
Pregnancy or breast feeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Deling Li, MD
Email
ttyyneuroli@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jingjing Zhang, MD.
Email
zhangjingjingtag@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nan Ji, MD
Organizational Affiliation
Beijing Tiantan Hospital, Capital Medical University Beijing 100050, China
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Zhaohui Zhu, MD.
Organizational Affiliation
Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
Official's Role
Study Director
Facility Information:
Facility Name
Beijing Tiantan Hospital, Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100050
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Deling Li, MD.
Phone
+86 10 69154196
Email
ttyyneuroli@126.com
12. IPD Sharing Statement
Learn more about this trial
IRDye800CW-BBN PET-NIRF Imaging Guiding Surgery in Patients With Glioblastoma
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