Breast Cancer Clinical Trial

F18 EF5 PET/CT Imaging in Patients With Brain Metastases From Breast Cancer

Summary

To estimate the presence of hypoxia in individual lesions after radiotherapy in patients with brain metastases from breast cancer as identified by F18 EF5 PET/CT imaging.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subjects with measurable brain metastases of at least 1 cm in any plane based on anatomic imaging.
Subjects with prior resection of brain metastases with progressions on brain MRI.
Histologic confirmation of breast cancer.
Age of study subject must be > 18 years.
ECOG Performance Status ≤ 2.
Ability to undergo brain MR and PET imaging
Study subjects must have normal organ and marrow function as defined below:

WBC >2,000/mmᶟ, platelets >90,000/mmᶟ, total bilirubin <2.0 mg/dl, creatinine <2.0 mg/dl.

The effects of EF5 on the developing human fetus are unknown. For this reason, women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control) prior to study entry and for the duration of study participation (1 month). Should a woman become pregnant pr suspect she is pregnant while participating in this study, she should inform her treating physician immediately. Women of childbearing potential will have a urine pregnancy test the day of the F18 -EF5 PET scan prior to the F18 -EF5 injection.
Ability to understand, participate and provide a documented signed informed consent.
Subjects who are allergic to gadolinium will have MRI scans without gadolinium contrast.

Exclusion Criteria:

History of allergic reactions attributed to Flagyl (metronidazole), which has a chemical structure similar to EF5.
Pregnant women are excluded because EF5 has an unknown risk for adverse events in fetuses and nursing infants secondary the administration of EF5 to the mother. Breastfeeding should be discontinued if EF5 is administered to the mother.
Subject has any other condition or personal circumstance that, in the judgement of the investigator, might interfere with the collection of complete good quality data.
Subjects who are unable to provide informed consent.
Patients with prior whole brain radiotherapy.
Patients with moderate to severe renal failure, defined as estimated GFR less than 30 ml/Lmin 1.73m²

Study is for people with:

Breast Cancer

Estimated Enrollment:

2

Study ID:

NCT01985971

Recruitment Status:

Completed

Sponsor:

Abramson Cancer Center of the University of Pennsylvania

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There is 1 Location for this study

See Locations Near You

Abramson Cancer Center of the University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

2

Study ID:

NCT01985971

Recruitment Status:

Completed

Sponsor:


Abramson Cancer Center of the University of Pennsylvania

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider