FLT: 18F-fluorothymidine

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PET using 11C- or 18F-labeled DNA precursors has a potential for specific imaging of proliferation in vivo. 11C-thymidine represents the native thymidine molecule and has been evaluated in preclinical and clinical studies . However, because of the rapid in vivo degradation and short half-life of 11C, this tracer was regarded as inappropriate for routine clinical use. In 1998, Shields et al. introduced 3'-deoxy-3'-18F-fluorothymidine (FLT) as a thymidine analog that is resistant to in vivo degradation and accumulates predominantly in proliferating tissues




124Iodine Imaging by PET

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Radioiodine kinetics and, hence, LDpA of DTC metastases showed great variability. For that reason, multiple 124I PET investigations are required. The 5-point protocol is certainly the most accurate among the approaches investigated, but the adapted 24-96-h approach using 2 points is an optimal dosimetry protocol when the clinical workload is particularly heavy, reducing logistical and time demands for patients and caregivers and clinical costs
 

 
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