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FET-PET for Evaluation of Response of Recurrent GBM to Avastin

Primary Purpose

Glioblastoma Multiforme, GBM

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
18F-FET
Sponsored by
Marcelo F. Di Carli, MD, FACC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Glioblastoma Multiforme focused on measuring FET, Fluoroethyl tyrosine, GBM, Response to treatment, Avastin, Brain Tumor

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1. GBM patients with changes on MRI suggestive of recurrence who have not yet initiated antiangiogenic therapy. 2. Age ≥ 18 3. Anticipated survival >3 months 4. Able to give informed consent 5. Capable of undergoing scan without the need for sedation or general anesthesia.

Exclusion Criteria:

  1. Active intracranial infection or nonglial brain mass.
  2. Recent large intracranial hemorrhage (<1 month; size to be determined by principal investigator)
  3. Pregnant or nursing. Quantitative serum hCG testing will be performed prior to the initial and each -subsequent FET- PET scan on all females of childbearing potential. Our BWH Radiation Safety Committee and Partners IRB requires stat serum ß-hcG pregnancy tests.
  4. Patient lives too far from BWH and/or is unwilling/ unable to return for scheduled imaging visits.

    -

Sites / Locations

  • Brigham and Women's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

GBM Avastin receiving 18F-FET

Arm Description

Recurrent GBM patients receiving Avastin, imaged twice with 18F-FET PET before and approximately 8 weeks after receiving Avastin

Outcomes

Primary Outcome Measures

Progression-free Survival
The primary objective is to assess the utility of FET-PET imaging for prediction of progression-free survival in recurrent glioblastoma.

Secondary Outcome Measures

Overall Survival
The secondary objective is to assess the utility of FET-PET imaging for prediction of overall survival in recurrent glioblastoma.

Full Information

First Posted
December 20, 2012
Last Updated
October 25, 2019
Sponsor
Marcelo F. Di Carli, MD, FACC
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1. Study Identification

Unique Protocol Identification Number
NCT01756352
Brief Title
FET-PET for Evaluation of Response of Recurrent GBM to Avastin
Official Title
Assessment of the Utility of the Radiotracer "FET"in PET Imaging of Recurrent Glioblastoma Multiforme (GBM): Monitoring Early Response to Antiangiogenic Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
September 13, 2015 (Actual)
Study Completion Date
September 13, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Marcelo F. Di Carli, MD, FACC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypothesis: The central hypothesis underlying the proposed research study is that FET-PET will predict durable benefit in patients receiving anti-angiogenic benefit for presumed recurrent GBM (i.e. progression-free survival and overall survival). We have defined one primary specific aim, for which we expect to obtain definitive results, and two secondary aims, under which we plan to generate preliminary data to support a future, larger project.
Detailed Description
The PET radiotracer FET provides a measure of large, neutral amino acid transport. This transport is significantly upregulated in malignant brain tumors. FET rarely gives false positive findings in the setting of inflammation seen after high dose chemotherapy or radiotherapy. FET labels low-grade as well as high-grade gliomas, in contrast to FDG, which almost exclusively labels only high-grade gliomas. FET imaging may prove to be particularly useful in the setting of infiltrative tumor, which is not contrast-enhancing on MRI and therefore not detectable with FDG. Management of glioblastoma patients with stable contrast-enhancing disease on MRI but increased signs of edema is difficult. This is because it is difficult to distinguish simple edema from infiltrative tumor. The former is managed with steroids and the latter is managed with chemotherapy, and anti-angiogenic drugs. FET may be particularly useful in assessing changes after GBM patients receive anti-vascular agents such as Avastin. Avastin is very commonly used in patients after failure of first-line treatment in GBM. Not only is Avastin costly, but it also can have serious side effects such as internal bleeding and gastric perforation, severe hypertension, poor wound healing, and renal toxicity. It is important to know when a patient is failing Avastin treatment so that the drug can be discontinued. Preliminary data in Europe (see figures below) suggests that FET-PET can accurately distinguish Avastin responders from non-responders. Inclusion Criteria: GBM patients with changes on MRI suggestive of recurrence who have not yet initiated antiangiogenic therapy. Age ≥ 18 Anticipated survival >3 months Able to give informed consent Capable of undergoing scan without the need for sedation or general anesthesia. Exclusion Criteria: Active intracranial infection or nonglial brain mass. Recent large intracranial hemorrhage (<1 month; size to be determined by principal investigator) Pregnant or nursing. Quantitative serum hCG testing will be performed prior to the initial and each -subsequent FET- PET scan on all females of childbearing potential. Our BWH Radiation Safety Committee and Partners IRB requires stat serum ß-hcG pregnancy tests. Patient lives too far from BWH and/or is unwilling/ unable to return for scheduled imaging visits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma Multiforme, GBM
Keywords
FET, Fluoroethyl tyrosine, GBM, Response to treatment, Avastin, Brain Tumor

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
GBM Avastin receiving 18F-FET
Arm Type
Experimental
Arm Description
Recurrent GBM patients receiving Avastin, imaged twice with 18F-FET PET before and approximately 8 weeks after receiving Avastin
Intervention Type
Drug
Intervention Name(s)
18F-FET
Other Intervention Name(s)
18F-Fluoroethyltyrosine
Intervention Description
Radiotracer, surrogate marker for protein synthesis
Primary Outcome Measure Information:
Title
Progression-free Survival
Description
The primary objective is to assess the utility of FET-PET imaging for prediction of progression-free survival in recurrent glioblastoma.
Time Frame
From date of baseline PET scan until the date of death from any cause, assessed up to 2 years.
Secondary Outcome Measure Information:
Title
Overall Survival
Description
The secondary objective is to assess the utility of FET-PET imaging for prediction of overall survival in recurrent glioblastoma.
Time Frame
From date of baseline PET scan until the date of death from any cause, assessed up to 2 years.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. GBM patients with changes on MRI suggestive of recurrence who have not yet initiated antiangiogenic therapy. 2. Age ≥ 18 3. Anticipated survival >3 months 4. Able to give informed consent 5. Capable of undergoing scan without the need for sedation or general anesthesia. Exclusion Criteria: Active intracranial infection or nonglial brain mass. Recent large intracranial hemorrhage (<1 month; size to be determined by principal investigator) Pregnant or nursing. Quantitative serum hCG testing will be performed prior to the initial and each -subsequent FET- PET scan on all females of childbearing potential. Our BWH Radiation Safety Committee and Partners IRB requires stat serum ß-hcG pregnancy tests. Patient lives too far from BWH and/or is unwilling/ unable to return for scheduled imaging visits. -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raymond L Huang, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Learn more about this trial

FET-PET for Evaluation of Response of Recurrent GBM to Avastin

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