کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3466239 | 1596559 | 2014 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Appropriate use of positron emission tomography with [18F]fluorodeoxyglucose for staging of oncology patients Appropriate use of positron emission tomography with [18F]fluorodeoxyglucose for staging of oncology patients](/preview/png/3466239.png)
• We examined the role of PET/CT in staging of several most-common cancer.
• We examined results in the literature in the last few years.
• We analysed cancers by site.
• We pointed out the appropriate and inappropriate uses of PET/CT in cancer staging.
• We stressed potential usefulness and pitfalls in PET/CT use in cancer staging.
Positron emission tomography (PET) was developed in the mid-1970, and its initial applications were for heart and brain imaging research. Nowadays, this technology is aimed mainly at staging or restaging tumours as it allows the assessment of biochemical processes that are either specific or associated with tumour biology.The full appreciation of PET potentials and limitations among general practitioners and internists cannot be considered achieved and the appropriate use of PET especially when coupled to X-ray computed tomography (CT) is still suboptimal.The majority of PET studies rely on the use of fluorodeoxyglucose labelled with fluorine-18 (FDG), which is a radiopharmaceutical specific for glucose transport and metabolism.PET with FDG is amenable for studying most type of tumours, including those of the head and neck, lung, oesophagus, colo-rectal, gastrointestinal stromal tumours, pancreas, some types of lymphomas and melanoma, whereas in some tumours, including those of the reproductive system, brain, breast and bones, there is a limited role for PET and there is no substantial role for FDG-PET for the bronchoalveolar, hepatocellular, urinary system, testicular, neuroendocrine, carcinoids and adrenal tumours, differentiated thyroid cancers, and several subtypes of malignant lymphoma. Thus, the limits of FDG have stimulated the use and development of other radiopharmaceuticals. These tracers represent the opportunity for expanding the use of PET to other areas in oncology in the near future.
Journal: European Journal of Internal Medicine - Volume 25, Issue 1, January 2014, Pages 6–11