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First published online February 20, 2008, 10.2967/jnumed.107.047506
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Journal of Nuclear Medicine Vol. 49 No. 3 367-374
© 2008 by Society of Nuclear Medicine

doi: 10.2967/jnumed.107.047506

Clinical Investigation

Quantitative Imaging of Estrogen Receptor Expression in Breast Cancer with PET and 18F-Fluoroestradiol

Lanell M. Peterson1, David A. Mankoff1, Thomas Lawton2, Kevin Yagle1, Erin K. Schubert1, Svetlana Stekhova1, Allen Gown3, Jeanne M. Link1, Timothy Tewson4 and Kenneth A. Krohn1

1 Department of Radiology, University of Washington/Seattle Cancer Care Alliance, Seattle, Washington; 2 Department of Pathology, University of Washington/Seattle Cancer Care Alliance, Seattle, Washington; 3 Phenopath Laboratories, Seattle, Washington; and 4 Department of Nuclear Medicine, University of Iowa, Iowa City, Iowa

Correspondence: For correspondence or reprints contact: David A. Mankoff, MD, PhD, Department of Radiology, Seattle Cancer Care Alliance, 825 Eastlake Ave. East, Mail Stop 62-600, Seattle, WA 98109. E-mail: dam{at}u.washington.edu

The PET compound 18F-fluoroestradiol (18F-FES) has been developed and tested as an agent for the imaging of estrogen receptor (ER) expression in vivo. 18F-FES uptake has been shown to correlate with ER expression assayed in vitro by radioligand binding; however, immunohistochemistry (IHC) rather than radioligand binding is used most often to measure ER expression in clinical practice. We therefore compared 18F-FES uptake with ER expression assayed in vitro by IHC with both qualitative and semiquantitative measures. Methods: Seventeen patients with primary or metastatic breast cancer were studied with dynamic 18F-FES PET; cancer tissue samples, collected close to the time of imaging, were assayed for ER expression by IHC. For each tumor, partial-volume-corrected measures of 18F-FES uptake were compared with ER expression measured by 3 different ER scoring methods: qualitative scoring (0–3+), the Allred score (0–10), and a computerized IHC index. Results: There was excellent agreement (r = 0.99) between observers using IHC as well as the different methods of measuring ER content (P < 0.001). ER-negative tumors had 18F-FES partial-volume-corrected standardized uptake values of less than 1.0, whereas ER-positive tumors had values above 1.1. Correlation coefficients for the different measures of ER content and the different measures of 18F-FES uptake ranged from 0.57 to 0.73, with the best correlation being between the computerized IHC index and 18F-FES partial-volume-corrected standardized uptake values. Conclusion: Our results showed good agreement between 18F-FES PET and ER expression measured by IHC. 18F-FES imaging may be a useful tool for aiding in the assessment of ER status, especially in patients with multiple tumors or for tumors that are difficult to biopsy.

Key Words: estrogen receptor • breast cancer • 18F-FES PET • IHC • tracer uptake

COPYRIGHT © 2008 by the Society of Nuclear Medicine, Inc.


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