TY - JOUR T1 - Fetal Dose Estimates for <sup>18</sup>F-Fluoro-<span class="sc">l</span>-Thymidine Using a Pregnant Monkey Model JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 288 LP - 292 DO - 10.2967/jnumed.109.068734 VL - 51 IS - 2 AU - Rachel M. Bartlett AU - Robert J. Nickles AU - Todd E. Barnhart AU - Bradley T. Christian AU - James E. Holden AU - Onofre T. DeJesus Y1 - 2010/02/01 UR - http://jnm.snmjournals.org/content/51/2/288.abstract N2 - Estimating the radiation dose received by the fetus from nuclear medicine procedures is important because of the greater sensitivity of rapidly developing fetal tissues to ionizing radiation. 18F-fluoro-l-thymidine (FLT) uptake is related to cellular proliferation and is currently used to monitor tumor progression and response to therapy. This study was undertaken to estimate—on the basis of biodistribution data obtained by PET/CT in pregnant rhesus monkeys—radiation absorbed dose to a human fetus administered 18F-FLT. Methods: Three pregnant rhesus macaques (gestational age, 113 ± 8 d) were administered 18F-FLT and imaged for 2 h on a PET/CT scanner. Time–activity curves for maternal and fetal organs were generated in anatomic regions of interest identified via CT. Doses were estimated using OLINDA/EXM and the 6-mo-pregnant human model. Results: The extrapolated whole-body maternal dose obtained, 11.4 μGy/MBq, is similar to the previously reported adult female dose of 15.6 μGy/MBq. The estimated total-body dose to a human fetus is 24 μGy/MBq. Significant long-term 18F-FLT accumulation in fetal liver resulted in a fetal liver dose of 53 μGy/MBq. Conclusion: The fetal dose estimate in a 6-mo-pregnant human using 18F-FLT is slightly greater than that reported for 18F-FDG. 18F-FLT trapping in the fetal liver should be considered in the risk–benefit analysis of 18F-FLT PET examination in pregnant patients. ER -