Table 1.
Modality | Indication | Advantages | Disadvantages |
---|---|---|---|
Radionuclide imaging | |||
Positron emission tomography | Detection | Wide range of molecular imaging probes | Limited spatial resolution (improved with use of non-contrast computed tomography) |
Response evaluation Tumor characterization |
Tracer imaging without perturbing biologic system | ||
Some radiation exposure | |||
Positron emission mammography |
Detection Tumor characterization |
More sensitive for smaller tumors Higher spatial resolution |
Increased radiation dose Visualization of posterior lesions Variable uptake of 18F-fluorodeoxyglucose (FDG) in small and less metabolically active tumors |
Breast-specific gamma imaging | Detection | More sensitive for smaller tumors Heavy compression of breast tissue not required |
Associated with radiation exposure Best combined with anatomic imaging (mammography) for optimal screening Longer imaging time |
Some radiation exposure | |||
Magnetic resonance | |||
Magnetic resonance imaging (MRI), especially dynamic contrast-enhanced MRI and targeted contrast agents |
Tumor characterization | Quantification of tumor perfusion and tumor capillary permeability |
Confined space Contrast design limited by need for magnetic atom |
Magnetic resonance spectroscopy | Tumor characterization | Can measure wide range of molecules No contrast necessary |
Limited spatial resolution Challenging to obtain high-quality spectra in routine imaging |
Ultrasound, especially with contrast enhancement |
Detection Tumor characterization |
Highly portable, inexpensive Molecular microbubble agents possible |
Operator dependence Contrast agents confined to vascular space thus far |
Optical imaging | Tumor characterization | Inexpensive, highly portable, and does not necessarily require a contrast agent |
Limited depth penetration, challenging spatial localization, and operator dependence |