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http://dx.doi.org/10.1016/j.eururo.2013.08.053DOI Listing

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Article Synopsis
  • The study focuses on identifying effective treatment responses in patients with metastatic castration-resistant prostate cancer (mCRPC) using positron emission tomography (PET) with different radiotracers.
  • A total of 49 patients were randomly assigned to receive scans using C-Choline, F-FACBC, or Ga-PSMA before treatment and again 2 months later to evaluate their biochemical response, primarily looking for a PSA reduction of ≥50%.
  • Results indicated that variations in metabolic tumor volume (MTV) and total lesion activity (TLA) with Ga-PSMA PET were significantly associated with treatment responses and could also predict progression-free survival and overall survival in patients.
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Following the previous part of the narrative review on artificial intelligence (AI) applications in positron emission tomography (PET) using tracers rather than F-fluorodeoxyglucose ([F]F-FDG), in this part we review the impact of PET-derived radiomics data on the diagnostic performance of other PET radiotracers, F-O-(2-fluoroethyl)-L-tyrosine ([F]F-FET), F-Fluorothymidine ([F]F-FLT) and C-Methionine ([C]C-MET). [F]F-FET-PET, using an artificial amino acid taken up into upregulated tumoral cells, showed potential in lesion detection and tumor characterization, especially with its ability to reflect glioma heterogeneity. [F]F-FET-PET-derived textural features appeared to have the potential to reveal considerable information for accurate delineation for guiding biopsy and treatment, differentiate between low-grade and high-grade glioma and related wild-type genotypes, and distinguish pseudoprogression from true progression.

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Background: F-Fluciclovine ([F]FACBC) has been recently proposed as a synthetic radiolabeled amino acid for positron emission tomography (PET) imaging in patients with brain neoplasms. Our aim is to evaluate the diagnostic performance of [F]FACBC PET in high-grade glioma (HGG) patients, taking into account the literature data.

Methods: A comprehensive literature search was performed.

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Background: Breast cancer is the most common malignancy in women, with high morbidity and mortality. Molecular alterations in breast cancer involve the expression or upregulation of various molecular targets that can be used for diagnostic nuclear medicine imaging and radiopharmaceutical treatment. Theragnostics is based on the binding of radionuclides to molecular targets.

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Purpose: [F]FDG PET/CT in multiple myeloma (MM) is currently the best technology to demonstrate patchy and extramedullary disease. However, [F]FDG PET has some limitations, and imaging with alternative tracers should be explored. In this study, we aimed to evaluate the performance of [F]fluciclovine PET compared to [F]FDG PET in newly diagnosed MM patients.

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