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

M

Marcelo F. Di Carli, MD, FACC

Status and phase

Completed
Phase 2

Conditions

Glioblastoma Multiforme
GBM

Treatments

Drug: 18F-FET

Study type

Interventional

Funder types

Other

Identifiers

NCT01756352
2012P002678

Details and patient eligibility

About

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.

Full 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:

  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.

Enrollment

13 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No 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.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

13 participants in 1 patient group

GBM Avastin receiving 18F-FET
Experimental group
Description:
Recurrent GBM patients receiving Avastin, imaged twice with 18F-FET PET before and approximately 8 weeks after receiving Avastin
Treatment:
Drug: 18F-FET

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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