AI Article Synopsis

  • The study evaluates the effectiveness of [C]methionine PET (MET-PET) versus [F]fluorodeoxyglucose PET (FDG-PET) in detecting cancer, particularly in tumors located in the trunk, like prostate and breast cancers.
  • Unlike FDG-PET, which has limitations due to the moderate glucose uptake in cancers, MET-PET leverages the stronger reliance of tumors on methionine for better imaging results.
  • Results showed that MET-PET is superior to FDG-PET in identifying and delineating both primary and metastatic tumors, suggesting it could guide potential methionine-restriction therapy for patients.

Article Abstract

Background/aim: Positron emission tomography (PET) is an important imaging modality, especially in oncology. [F]fluorodeoxyglucose PET (FDG-PET) is the most used cancer PET imaging. However, since the elevated glucose use by cancers, termed the Warburg effect, is usually only moderate, FDG often does not provide a strong or well-delineated signal. Malignancies have a stronger addiction to methionine, known as the Hoffman effect, and thus [C]methionine PET (MET-PET) has demonstrated superiority over FDG-PET in gliomas and other brain tumors. Our team is pioneering the use of MET-PET for tumors of the trunk for both better detection of cancer and to determine candidates for methionine-restriction therapy. The present study provides examples of cancers of organs in the trunk in which MET-PET outperforms FDG-PET in detecting and delineating primary and metastatic cancer.

Patients And Methods: In all cases, MET-PET and FDG-PET were performed simultaneously. An evaluation of the images was conducted by a nuclear medicine physician.

Results: Four cases, including prostate, bladder, esophageal, and breast cancer demonstrated the superiority of MET-PET compared to FDG-PET.

Conclusion: MET-PET can out-perform FDG PET for accurate detection of primary and metastatic cancer in the trunk and can determine the extent of methionine addiction of cancer, thereby indicating whether cancer patients can benefit from methionine-restriction therapy.

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Source
http://dx.doi.org/10.21873/anticanres.17216DOI Listing

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