JNM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH RSS TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zanzonico, P. B.
Right arrow Articles by Humm, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zanzonico, P. B.
Right arrow Articles by Humm, J. L.
Journal of Nuclear Medicine Vol. 45 No. 11 1966-1971
© 2004 by Society of Nuclear Medicine


Basic Science Investigations

PET-Based Radiation Dosimetry in Man of 18F-Fluorodihydrotestosterone, a New Radiotracer for Imaging Prostate Cancer

Pat B. Zanzonico, PhD1, Ronald Finn, PhD1, Keith S. Pentlow, MS1, Yusuf Erdi, DSc1, Bradley Beattie, MS1, Timothy Akhurst, MD1, Olivia Squire, BA1, Michael Morris, MD1, Howard Scher, MD1, Timothy McCarthy, PhD2, Michael Welch, PhD2, Steven M. Larson, MD1 and John L. Humm, PhD1

1 Memorial Sloan-Kettering Cancer Center, New York, New York
2 Washington University, St. Louis, Missouri

16ß-fluoro-5{alpha}-dihydrotestosterone (FDHT) is a promising new PET radiopharmaceutical for the imaging of prostate cancer. A recent clinical trial provided the opportunity for refinement of normal-tissue radiation-absorbed dose estimates based on quantitative PET. The objective of the current study was to derive estimates of normal-tissue absorbed doses for 18F-FDHT administered to patients with advanced prostate cancer. Methods: Absorbed dose estimates were derived from 10 18F-FDHT PET studies (administered activity, 111–407 MBq) of 7 prostate cancer patients. Activity concentrations in plasma and red marrow (assuming a plasmacrit of 0.58, an extracellular fluid fraction of 0.40, and equilibration of activity between plasma and marrow extracellular fluid) were measured ex vivo from a peripheral blood sample. Liver, spleen, urinary bladder contents, and total-body activities were measured by region-of-interest analysis of quantitative whole-body studies acquired with a dedicated PET scanner. Total organ activities and residence times were calculated from the respective PET scan-derived activity concentrations assuming standard (70 kg) man organ masses. Urinary excretion was corrected for hepatobiliary excretion (liver activity), and a first-order adjustment was made for the bladder-wall mass based on the patient’s total-body mass. Mean organ absorbed doses were calculated with the MIRD formalism and the standard man model using the MIRDOSE3 software program. Results: The absorbed doses (mean ± SD) ranged from 0.00057 ± 0.000281 cGy/MBq (to skin) to 0.00868 ± 0.00481 cGy/MBq (to bladder wall) (voiding intervals, 1–2 h), and the effective dose equivalent was 0.00177 ± 0.000152 cSv/MBq. Conclusion: The maximum absorbed dose among all tissues in all 10 studies, 0.0151 cGy/MBq, occurred for the urinary bladder wall (with hydration and 1- to 2-h voiding intervals). To ensure that the maximum normal-tissue absorbed dose is kept below the recommended maximum permissible dose of 5 cGy per single administration, a maximum administered activity of 331 MBq (5 cGy/[0.0151 cGy/MBq]) is recommended for 18F-FDHT.

Key Words: FDHT • dosimetry • prostate cancer • 18F • androgens




This article has been cited by other articles:


Home page
JNMHome page
B. J. Beattie, P. M. Smith-Jones, Y. S. Jhanwar, H. Schoder, C. R. Schmidtlein, M. J. Morris, P. Zanzonico, O. Squire, G. S.P. Meirelles, R. Finn, et al.
Pharmacokinetic Assessment of the Uptake of 16{beta}-18F-Fluoro-5{alpha}-Dihydrotestosterone (FDHT) in Prostate Tumors as Measured by PET
J. Nucl. Med., February 1, 2010; 51(2): 183 - 192.
[Abstract] [Full Text] [PDF]


Home page
JNMHome page
B. Zhao, L. H. Schwartz, and S. M. Larson
Imaging Surrogates of Tumor Response to Therapy: Anatomic and Functional Biomarkers
J. Nucl. Med., February 1, 2009; 50(2): 239 - 249.
[Abstract] [Full Text] [PDF]


Home page
JNMHome page
E. E. Parent, C. S. Dence, T. L. Sharp, M. J. Welch, and J. A. Katzenellenbogen
7{alpha}-18F-Fluoromethyl-Dihydrotestosterone and 7{alpha}-18F-Fluoromethyl-Nortestosterone: Ligands to Determine the Role of Sex Hormone-Binding Globulin for Steroidal Radiopharmaceuticals
J. Nucl. Med., June 1, 2008; 49(6): 987 - 994.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
J. L. Speight and M. Roach III
Advances in the Treatment of Localized Prostate Cancer: The Role of Anatomic and Functional Imaging in Men Managed With Radiotherapy
J. Clin. Oncol., March 10, 2007; 25(8): 987 - 995.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
G. J. Kelloff, K. A. Krohn, S. M. Larson, R. Weissleder, D. A. Mankoff, J. M. Hoffman, J. M. Link, K. Z. Guyton, W. C. Eckelman, H. I. Scher, et al.
The Progress and Promise of Molecular Imaging Probes in Oncologic Drug Development
Clin. Cancer Res., November 15, 2005; 11(22): 7967 - 7985.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH RSS TABLE OF CONTENTS
JOURNAL OF NUCLEAR MEDICINE TECHNOLOGY THE JOURNAL OF NUCLEAR MEDICINE
Copyright © 2004 by the Society of Nuclear Medicine.