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Diagnostic Performance of Fluorescein as an Intraoperative Brain Tumor Biomarker

Primary Purpose

Brain Cancer

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Fluorescein
Fluorescein + ALA
Sponsored by
David W. Roberts
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Brain Cancer focused on measuring High Grade Glioma, Low Grade Glioma, Brain Tumor

Eligibility Criteria

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

Inclusion Criteria:

  1. Preoperative diagnosis of either presumed first-time low or high grade glioma (astrocytoma, oligodendroglioma, mixed oligo-astrocytoma, anaplastic astrocytoma, and glioblastoma multiforme).
  2. Tumor judged to be suitable for open cranial resection based on preoperative imaging studies.
  3. Valid informed consent by subject or subject's LAR.
  4. No serious associated psychiatric illnesses.
  5. Age ≥ 21 years old.

Exclusion Criteria:

  1. Pregnant women or women who are breast feeding.
  2. History of hypersensitivity to fluorescein.
  3. History of cutaneous photosensitivity, porphyria, hypersensitivity to porphyrins, photodermatosis, exfoliative dermatitis.
  4. History of liver disease within the last 12 months.
  5. Elevated LFTs (AST, ALT, ALP or bilirubin levels greater than 2.5 times the normal limit) from laboratory tests conducted within 30 days prior to surgery.
  6. Serum creatinine in excess of 180µmol/L (2.04 md/dL) within 30 days prior to surgery.
  7. Inability to comply with the photosensitivity precautions associated with the study.

Sites / Locations

  • Sally B MansurRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Fluorescein

Fluorescein + ALA

Arm Description

Fluorescein administered IV at 5mg/kg approximately 30 minutes prior to the beginning of the tumor resection. A second injection may occur if the fluorescein fluorescence is dissipated substantially during the course of the procedure.

Fluorescein administered IV at 5mg/kg approximately 30 minutes prior to the beginning of the tumor resection. A second injection may occur if the fluorescein fluorescence is dissipated substantially during the course of the procedure. ALA administered orally at 20mg/kg approximately 3 hours before surgery.

Outcomes

Primary Outcome Measures

Fluorescein performance as an intraoperative biomarker for tumor tissue will be reported.
The predictive performance of fluorescein fluorescence as an intraoperative imaging biomarker of tumor during surgery in patients with a clinical diagnosis of high grade glioma (HGG) and patients with a clinical diagnosis of low grade glioma (LGG) will be measured. Fluorescence will be measured both quantitatively via an intraoperative probe and visually by the neurosurgeon through the operating microscope. Endpoints will be assessed separately for HGG and LGG groups.

Secondary Outcome Measures

Fluorescein performance as visualized and measured with an intraoperative probe will be reported
The performance of fluorescein as visualized by the neurosurgeon and measured quantitatively with an intraoperative probe will be analyzed to the contrast-enhancement on coregistered preoperative MR scans in patients with a clinical diagnosis of high grade glioma.
Fluorescein versus fluorescein + ALA performance will be reported in patients in patients with 2 different types of tumors
The performance of fluorescein versus fluorescein + ALA as visualized by the neurosurgeon and measured quantitatively with an intra-operative probe will be analyzed in patients with a clinical diagnosis of either high grade glioma (HGG) or low grade glioma (LGG).

Full Information

First Posted
February 22, 2016
Last Updated
May 16, 2023
Sponsor
David W. Roberts
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS), Carl Zeiss Meditec, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02691923
Brief Title
Diagnostic Performance of Fluorescein as an Intraoperative Brain Tumor Biomarker
Official Title
Diagnostic Performance of Fluorescein as an Intraoperative Brain Tumor Biomarker: Correlation With Preoperative MR, ALA-induced PpIX Fluorescence, and Histopathology
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 2016 (undefined)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
David W. Roberts
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS), Carl Zeiss Meditec, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This clinical research will evaluate the diagnostic potential of fluorescein as visualized through an operating microscope relative to 1) contrast enhancement on co-registered preoperative MR scans, 2) intraoperative ALA-induced PpIX fluorescence and 3) gold-standard histology obtained from biopsy sampling during the procedure. Subjects will include those people with operable brain tumor with first-time presumed pre-surgical diagnosis of high-grade glioma or low-grade glioma.
Detailed Description
Consenting subjects who have met inclusion and exclusion criteria will be enrolled to receive either fluorescein+ALA or fluorescein alone. HGG patients will be randomized on a 2 to 1 basis to receive either both fluorescein and ALA or fluorescein alone, and LGG patients will be randomized on a 1 to 1 basis. This study is a diagnostic trial of fluorescein fluorescence as an intraoperative imaging biomarker during open cranial surgery for tumor resection of first-time (preoperatively) presumed high or low grade glioma. Subjects participate in a "one-time" event/visit (i.e, surgery) as part of this protocol. Images and data from the patient's pre- and post-operative MR scans are used for analysis in the study, but these acquisitions are part of the patient's standard-of-care, would occur independently of whether the participant is enrolled; and thus, are not considered to be research study visits. No post-surgical follow-up visit is part of the protocol data collection or analysis. Patients are monitored for possible adverse events through the routine follow-up under the care of the operating surgeon involved in the study procedures, post-operatively and subsequently through the medical record. Hence, this information is already being collected as part of standard-of-care and is available for adverse event surveillance. Patients receiving ALA who present with abnormally elevated LFTs beyond the peri-operative observation period are monitored on a regular basis until resolution and this blood testing is considered to be part of the study. Administration of study drug: Patients enrolled in the fluorescein+ALA arm will be administered orally 5-ALA (DUSA Pharmaceuticals, Tarrytown, NY) at 20 mg/kg body weight, dissolved in 100 ml of water, approximately 3 hours prior to the induction of anesthesia. For patients receiving only fluorescein, the operating surgeon will request bolus injection (at a dose of 5 mg/kg) approximately 30 minutes prior to the start of tumor resection. For especially long cases (e.g., > 4 h) or if fluorescein fluorescence dissipates substantially during the course of the procedure, a second bolus injection may occur later in the case.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Cancer
Keywords
High Grade Glioma, Low Grade Glioma, Brain Tumor

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fluorescein
Arm Type
Active Comparator
Arm Description
Fluorescein administered IV at 5mg/kg approximately 30 minutes prior to the beginning of the tumor resection. A second injection may occur if the fluorescein fluorescence is dissipated substantially during the course of the procedure.
Arm Title
Fluorescein + ALA
Arm Type
Experimental
Arm Description
Fluorescein administered IV at 5mg/kg approximately 30 minutes prior to the beginning of the tumor resection. A second injection may occur if the fluorescein fluorescence is dissipated substantially during the course of the procedure. ALA administered orally at 20mg/kg approximately 3 hours before surgery.
Intervention Type
Drug
Intervention Name(s)
Fluorescein
Other Intervention Name(s)
Fluorescite
Intervention Type
Drug
Intervention Name(s)
Fluorescein + ALA
Other Intervention Name(s)
Flourescein = Fluorescite; ALA = 5-Aminolevulinic Acid
Primary Outcome Measure Information:
Title
Fluorescein performance as an intraoperative biomarker for tumor tissue will be reported.
Description
The predictive performance of fluorescein fluorescence as an intraoperative imaging biomarker of tumor during surgery in patients with a clinical diagnosis of high grade glioma (HGG) and patients with a clinical diagnosis of low grade glioma (LGG) will be measured. Fluorescence will be measured both quantitatively via an intraoperative probe and visually by the neurosurgeon through the operating microscope. Endpoints will be assessed separately for HGG and LGG groups.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Fluorescein performance as visualized and measured with an intraoperative probe will be reported
Description
The performance of fluorescein as visualized by the neurosurgeon and measured quantitatively with an intraoperative probe will be analyzed to the contrast-enhancement on coregistered preoperative MR scans in patients with a clinical diagnosis of high grade glioma.
Time Frame
24 months
Title
Fluorescein versus fluorescein + ALA performance will be reported in patients in patients with 2 different types of tumors
Description
The performance of fluorescein versus fluorescein + ALA as visualized by the neurosurgeon and measured quantitatively with an intra-operative probe will be analyzed in patients with a clinical diagnosis of either high grade glioma (HGG) or low grade glioma (LGG).
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Preoperative diagnosis of either presumed first-time low or high grade glioma (astrocytoma, oligodendroglioma, mixed oligo-astrocytoma, anaplastic astrocytoma, and glioblastoma multiforme). Tumor judged to be suitable for open cranial resection based on preoperative imaging studies. Valid informed consent by subject or subject's LAR. No serious associated psychiatric illnesses. Age ≥ 21 years old. Exclusion Criteria: Pregnant women or women who are breast feeding. History of hypersensitivity to fluorescein. History of cutaneous photosensitivity, porphyria, hypersensitivity to porphyrins, photodermatosis, exfoliative dermatitis. History of liver disease within the last 12 months. Elevated LFTs (AST, ALT, ALP or bilirubin levels greater than 2.5 times the normal limit) from laboratory tests conducted within 30 days prior to surgery. Serum creatinine in excess of 180µmol/L (2.04 md/dL) within 30 days prior to surgery. Inability to comply with the photosensitivity precautions associated with the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sally B Mansur, MS
Email
Sally.B.Mansur@Dartmouth.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Keith D Paulsen, PhD
Email
Keith.D.Paulsen@Dartmouth.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David W Roberts, MD
Organizational Affiliation
Dartmouth-Hitchcock Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sally B Mansur
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03756
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sally B Mansur, MS
Email
Sally.B.Mansur@Dartmouth.edu
First Name & Middle Initial & Last Name & Degree
Keith D Paulsen, PhD
Email
Keith.D.Paulsen@Dartmouth.edu

12. IPD Sharing Statement

Citations:
PubMed Identifier
22748650
Citation
Roberts DW, Valdes PA, Harris BT, Hartov A, Fan X, Ji S, Leblond F, Tosteson TD, Wilson BC, Paulsen KD. Glioblastoma multiforme treatment with clinical trials for surgical resection (aminolevulinic acid). Neurosurg Clin N Am. 2012 Jul;23(3):371-7. doi: 10.1016/j.nec.2012.04.001.
Results Reference
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PubMed Identifier
26504628
Citation
Elliott JT, Dsouza AV, Davis SC, Olson JD, Paulsen KD, Roberts DW, Pogue BW. Review of fluorescence guided surgery visualization and overlay techniques. Biomed Opt Express. 2015 Sep 3;6(10):3765-82. doi: 10.1364/BOE.6.003765. eCollection 2015 Oct 1.
Results Reference
background
PubMed Identifier
26140489
Citation
Valdes PA, Jacobs V, Harris BT, Wilson BC, Leblond F, Paulsen KD, Roberts DW. Quantitative fluorescence using 5-aminolevulinic acid-induced protoporphyrin IX biomarker as a surgical adjunct in low-grade glioma surgery. J Neurosurg. 2015 Sep;123(3):771-80. doi: 10.3171/2014.12.JNS14391. Epub 2015 Jul 3.
Results Reference
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Diagnostic Performance of Fluorescein as an Intraoperative Brain Tumor Biomarker

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