2018
DOI: 10.1186/s41824-018-0039-x
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Positron emission tomography in breast cancer: 18F- FDG and other radiopharmaceuticals

Abstract: Background: Breast cancer heterogeneity reflects the complex biology of this disease. Breast cancer subtypes, as identified either by immunohistochemistry (IHC) or by gene expression analysis, present different molecular characteristics and prognosis. In this context, molecular imaging techniques providing functional information, contribute in evaluating response to treatment and long-term prognosis among different subtypes. Nuclear imaging diagnosis modalities play an important role for conducting research on… Show more

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Cited by 7 publications
(4 citation statements)
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References 99 publications
(104 reference statements)
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“…It is also used for the detection of dense breasts and lesions of 1 cm or less. It has limited use in clinical practice because of high dose exposure of radionuclide to patients hence only used I clinical trial investigation of breast cancer [44]. Positron emission mammography or PEM uses a lower dose of radionuclide and having a high spatial resolution as compared to PET.…”
Section: Radionuclide Methodsmentioning
confidence: 99%
“…It is also used for the detection of dense breasts and lesions of 1 cm or less. It has limited use in clinical practice because of high dose exposure of radionuclide to patients hence only used I clinical trial investigation of breast cancer [44]. Positron emission mammography or PEM uses a lower dose of radionuclide and having a high spatial resolution as compared to PET.…”
Section: Radionuclide Methodsmentioning
confidence: 99%
“…[ 18 F]FDG is considered a suboptimal radiopharmaceutical for imaging breast cancer as it is non-specific with substantial variations in uptake between breast tumour characteristics and breast cancer subgroups [22][23][24][25][26]. The use of tumour-specific tracers, targeting, for example, ER (e.g.…”
Section: Limitationsmentioning
confidence: 99%
“…a suture, would allow better correlation between FAR and histopathology. 18 F-FDG is considered a suboptimal radiopharmaceutical for imaging breast cancer as it is non-speci c with substantial variations in uptake between breast tumour characteristics and breast cancer subgroups [21][22][23][24][25]. The use of tumour-speci c tracers, targeting for example ER (e.g.…”
Section: Limitationsmentioning
confidence: 99%