Cerianna PET-CT: Identifying Patients Who May Benefit

Video Library - Breast Cancer
Gary Ulaner, MD, PhD, FACNM
James & Pamela Muzzy Endowed Chair in Molecular Imaging and Therapy
Hoag Family Cancer Institute
Presented by
Sponsored by
AONN+ is pleased to introduce a presentation on an FDA-approved PET imaging agent, Cerianna (fluoroestradiol F-18), which is used as an adjunct to biopsy for the detection of estrogen receptor (ER)-positive lesions to help inform treatment selection for patients with recurrent or metastatic breast cancer.
This presentation is a non-CE program filmed on November 20, 2021, at the 12th AONN+ Annual Navigation & Survivorship Conference. Topics of this presentation include:
  • Concept of molecular imaging
  • Role of Cerianna PET in estrogen receptor–targeted molecular imaging
  • Clinical applications of Cerianna PET that may improve patient care
Speaker:
Gary Ulaner, MD, PhD, FACNM
James & Pamela Muzzy Endowed Chair in Molecular Imaging and Therapy
Hoag Family Cancer Institute

Cerianna™ (fluoroestradiol F 18) Injection

Important Safety Information for Cerianna™ (fluoroestradiol F 18) Injection:

Limitations of Use - Tissue biopsy should be used to confirm recurrence of breast cancer and to verify ER status by pathology. CERIANNA is not useful for imaging other receptors, such as human epidermal growth factor receptor 2 (HER2) and the progesterone receptor (PR).

CONTRAINDICATIONS - None.

ADVERSE REACTIONS - In Clinical Trials (n=1207) the most common adverse reactions seen occurred at a rate <1% were injection-site pain and dysgeusia.

To report SUSPECTED ADVERSE REACTIONS, contact Zionexa US Corp, a GE Healthcare Company, at +1-844-946-6392, or the FDA at 1-800-FDA-1088, or www.fda.gov/medwatch.

For full Prescribing Information click here or visit cerianna.com/pi.