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Clinical Trial Summary

The purpose of this study is to assess the utility of FDG PET/CT in evaluating response of bone dominant breast cancer to therapy. Eligible patients with bone dominant ER+ breast cancer will undergo baseline FDG PET/CT for evaluation of their disease, after the start of therapy they will undergo an FDG PET/CT scan at 4 weeks and again at 12 weeks. PET/CT results will be compared to clinical measures of response, time to progression and overall survival.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02110160
Study type Observational
Source Abramson Cancer Center of the University of Pennsylvania
Contact David A. Mankoff, MD
Phone 855-216-0098
Email PennCancerTrials@emergingmed.com
Status Recruiting
Phase
Start date September 2013