๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-11-18

Brain [18F]-FES PET/CT in Patients With Estrogen-Receptor Positive Breast Cancer (NCT06072807)

Brain [18F]-FES PET/CT in the Diagnosis, Treatment Planning and Response Assessment of Brain Metastases in Patients With Estrogen-Receptor Positive Breast Cancer

๐ŸŸข Recruiting Phase4 ๐Ÿ“‹ Clinical Research Protocol Sponsor: Weill Medical College of Cornell University

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The goal of this interventional study is to optimize the protocol of FES PET/CT in Estrogen Receptor positive Breast cancer patients with Brain metastases. Patients will undergo MRI of the brain and FDG PET/CT brain as part of standard of care for radiation treatment planning. An additional 18F-FES PET/CT brain scan will be completed before this standard of care radiation treatment. Patients will be followed prospectively with clinical and MRI assessments per standard-of-care for a total of 12 months. Study Population: Patients with ER-positive breast cancer with biopsy proven or suspected new or recurrent brain metastases (based on standard of care MRI) planned for radiation treatment of brain lesions.

Who can join: Review the eligibility criteria below.

Location: New York-Presbyterian/Weill Cornell Medical Center โ€” New York, New York

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Brain Imaging with 18F-FES (DIAGNOSTIC_TEST)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • New York-Presbyterian/Weill Cornell Medical Center โ€” New York, New York

๐Ÿ“ž Contact the Study Coordinator

Phone: (212) 746-4587

Email: jai9018@med.cornell.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Breast Cancer clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—