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. 2008 Aug 20;26(24):4012–4021. doi: 10.1200/JCO.2007.14.3065

Table 2.

New Technologies for Human Cancer Imaging

Clinical Problem Cancer/Discipline New Technology Advantage Disadvantage Reference
Screening Breast Dedicated CT High resolution and sensitivity Ionizing radiation (same as 2-view mammogram) 15,16
PEM High sensitivity, moderate to high resolution Requires IV injection of radiotracer 17
DCE-MRI High resolution and specificity Requires IV injection of lanthanide chelate 19
Diffuse optical tomography (spectroscopy) Noncontrast study, safe, 3-D, quantitative, high specificity, can be combined with MRI Low resolution, low to moderate sensitivity 27-29
Endoscopy/colonoscopy/colposcopy Optical (diffuse reflectance) Fast, inexpensive, safe Surface imaging only, interference from blood 31
Optical (photon scattering) Fast, inexpensive, safe Surface imaging only, interference from blood 32-34
Optical (multi-wavelength spectroscopy) Fast, inexpensive, safe Surface imaging only, interference from blood 35
Optical (autofluorescence spectroscopy) Fast, inexpensive, safe Surface imaging only, interference from blood 36
Optical (polarization spectroscopy) Fast, inexpensive, safe Surface imaging only, interference from blood 37
Optical coherence tomography Fast, high resolution, safe Limited depth to ≈ 2 mm, endogenous contrast only 38,39
Exogenous fluorescence High sensitivity and specificity Requires IV injection of contrast agent 40-42
Virtual colonoscopy CT-based Noninvasive, relatively fast Uses ionizing radiation, difficulty with flat lesions and small polyps 43
MRI-based Noninvasive, relatively fast Difficulty with flat lesions and small polyps 44
Staging PET Replacements for SPECT radiotracers Higher sensitivity and resolution Desired half-life not always available 47
Time-of-flight detection 2-fold higher resolution or sensitivity Limited availability 48,49
MRI Hyperpolarization High sensitivity possible, in vivo tracking of molecule metabolism Relatively short relaxation times of agents tested to date 50,51
PARACEST Higher sensitivity than traditional lanthanide imaging Sensitivity not yet adequate for receptor-based imaging 53
All Low-molecular weight targeting ligands Rapid biodistribution and clearance Tumor contact time often inadequate 54-59
Signal amplification/background reduction (optical) Improved SBR Requires endocytosis and pH-dependent activation 60
Treatment Chemotherapy Image-guided treatment (18FDG-PET) Highly sensitive Expensive, not all tumors FDG-avid, difficult to quantify log kill 61-63
Image-guided treatment (99mTc-Annexin V) Moderately sensitive Presently unavailable, difficult to quantify log kill 64-66
Image-guided treatment (DCE-MRI) No ionizing radiation Requires intravenous injection of lanthanide chelate, difficult to quantify log kill 67
Image-guided treatment (optical spectroscopy) No ionizing radiation, fast, safe, quantitative, high sensitivity and specificity Low resolution, moderate sensitivity, difficult to quantify log kill 68
Radiotherapy Ion beam-induced PET and PET/CT Near real-time feedback on dose delivery Requires specialized and expensive infrastructure, difficult mathematical modeling 69
Surgery Optical (reflectance NIR fluorescence) Fast, real-time, high sensitivity and specificity Poor depth penetration (≈1-3 mm) 70-72,79,81,82,84
Optical (tomographic NIR fluorescence) Depth penetration up to several cm, quantitative, high specificity Requires separate acquisition and reconstruction, low to moderate resolution, low to moderate sensitivity 73

Abbreviations: CT, computed tomography; PEM, positron emission mammography; IV, intravenous; DCE, dynamic contrast-enhanced; MRI, magnetic resonance imaging; SPECT, single photon emission computed tomography; PARACEST, paramagnetic chemical exchange saturation transfer; SBR, signal-to-background ratio; 18FDG, 2-deoxy-2-[18F]fluoro-D-glucose; 99mTc, technetium 99m; NIR, near-infrared.