Affinity of PET-MRI Tracers for Hypoxic Cells in Breast Cancer: A Systematic Review.
Ioana-Claudia CostinLoredana G MarcuPublished in: Cells (2024)
Tumour hypoxia is a known microenvironmental culprit for treatment resistance, tumour recurrence and promotion of metastatic spread. Despite the long-known existence of this factor within the tumour milieu, hypoxia is still one of the greatest challenges in cancer management. The transition from invasive and less reliable detection methods to more accurate and non-invasive ways to identify and quantify hypoxia was a long process that eventually led to the promising results showed by functional imaging techniques. Hybrid imaging, such as PET-CT, has the great advantage of combining the structural or anatomical image (offered by CT) with the functional or metabolic one (offered by PET). However, in the context of hypoxia, it is only the PET image taken after appropriate radiotracer administration that would supply hypoxia-specific information. To overcome this limitation, the development of the latest hybrid imaging systems, such as PET-MRI, enables a synergistic approach towards hypoxia imaging, with both methods having the potential to provide functional information on the tumour microenvironment. This study is designed as a systematic review of the literature on the newest developments of PET-MRI for the imaging of hypoxic cells in breast cancer. The analysis includes the affinity of various PET-MRI tracers for hypoxia in this patient group as well as the correlations between PET-specific and MRI-specific parameters, to offer a broader view on the potential for the widespread clinical implementation of this hybrid imaging technique.
Keyphrases
- pet ct
- positron emission tomography
- high resolution
- computed tomography
- contrast enhanced
- magnetic resonance imaging
- pet imaging
- endothelial cells
- small cell lung cancer
- diffusion weighted imaging
- squamous cell carcinoma
- deep learning
- magnetic resonance
- machine learning
- quality improvement
- cell death
- cell cycle arrest
- climate change
- case report
- signaling pathway
- combination therapy
- replacement therapy