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It was found that 18F-alfatide PET identified all tumors, with mean standardized uptake values of 2.90 ± 0.10.
Interestingly, in addition to key regions for seizure generation in temporal lobe epilepsy, in vivo PET identified several other brain regions with moderate levels of increased TSPO binding such as the hypothalamus (Table 1) which was in case of the hypothalamus confirmed by in vitro binding and immunohistochemistry in the same animals (Table 2).
PET identified patients most likely to achieve a favourable response from subsequent high dose chemotherapy.
They found that in all but one case PET identified the site of disease.
PET identified all 128 abnormal sites identified by conventional imaging plus an additional 11 sites not previously recognised.
As recently reported by Tessonnier et al. in 4 patients with solitary insulinomas, FDOPA PET identified tumor in only one case.
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(1) Can PET identify the primary tumour more accurately?
In this review, three issues are discussed: First, can PET identify a tumour more accurately?
The following three issues are discussed: (1) Can PET identify the primary tumour more accurately?
Importantly, PET identifies more bone metastases than the planar RNB and F-PET/CT is able to detect more lesions than SPECT/CT.
If FDG PET identifies disease with greater resolution than conventional radiography, then presumably F-FDG may also be able to control more disease.
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