Table 1.
Imaging modality | Probe | Tumor Model or Clinical Trial | Major Findings | Ref. |
---|---|---|---|---|
PET | 89Zr-trastuzumab | SKBR3 xenografts | Detection of the changes in HER2 expression following treatment with DMAG | 22 |
PET | 89Zr-trastuzumab | Clinical trial | Quantification of the uptake is possible, optimally 4–5 days post injection | 23 |
PET |
124I-ZHER2:342 124I-trastuzumab |
NCI-N87 xenografts | Using 124I-ZHER2:342 resulted in higher tumor-to-organ ratios as compare to 124I-trastuzumab | 26 |
PET |
111In-ABY-002 68Ga-ABY-002 |
SKBR3 xenografts | Rapid clearance of 68Ga-ABY-002 blood and healthy tissues (except kidneys) resulted in high tumor to organ ratios as soon as 2 h after injection | 27 |
PET SPECT |
111In-ABY-002 68Ga-ABY-002 |
Clinical trial | High-contrast SPECT or PET images of HER2-positive tumors can be obtained in humans as soon as 2–3 h after injection | 28 |
PET |
64CU-DOTA-ZHER2:477 (64CU-DOTA-ZHER2:477)2 |
SKOV3 xenografts | Monomer resulted in higher tumor accumulation and tumor/blood ratio as compared to dimer | 29 |
PET | (18F-FBEM)-ZHER2:342 | SKOV3 xenografts | The readioactivity was eliminated quickly from the blood and normal tissues, including the kidneys and liver, providing high tumor/blood and tumor/muscle ratios as soon as 1 h post injection | 31 |
PET | 18F-FBEM-ZHER2:342 | BT474, MD-MBA-361,MCF7,and U251 xenogrfts | HER2 expression and its changes caused by therapeutic intervention can be monitored by PET | 32 |
PET | 68Ga-DOTA-MUT-DS | SKOV3 xenografts | The probe bound to HER2 with high affinity, was stable in mouse serum, had rapid and high tumor accumulation, and was quickly cleared from normal organs | 33 |
SPECT | 111In-DTPA-trastuzumab | MDA-MB-231,MDA-MB-361, SKBR-3,Bt-20, BT474, BY474het, MCF7/HER2-18 xenografts | Tumor response to Herceptin depends on HER2 expression | 34 |
SPECT | 111In-DTPA-pertuzumab | MDA-MB-361 xenografts | Decrease of 111In-DTPA-pertuzumab uptake following treatment with trastuzumab associated eradication of HER2-positive tumor cells | 35 |
SPECT | 99mTC-ZHER2:2395-CyS | LS174T, SKOV-3 xenografts | Rapid accumulation in HER2-positive xenografts and rapid clearance from a majority of organs (except for the kidneys and liver) allowed clear visualization of HER2 expression within a few hours after injection | 36 |
MRI | Trastuzumab-conjugated, dextran-modified iron oxide nanoparticles | BT-474, SKBR-3, MDA-MB-231, MCF-7 xenografts | The HER2-specific nanoparticles bound specially to HER2-positive cells and allowed visualization of HER2-posive xenografts by a 3-T MRI scanner using T2-weighted fast spin-echo sequence | 37 |
MRI | Affibody-SPIO nanoparticles | SKOV-3 xenografts | The nanoparticles bound specifically to HER2, and the tumor could be clearly seen imaged on MRI using a gradient-echo sequence | 38 |
Optical Imaging | 111In and indocyanine green-labeled trastuzumab | MDA-MB-468, A431, 3T3/HER2 xenografts | Multimodality imaging following injection of dual labeled, radio-optical probes provides data on biodistribution profile of the injected antibody by nuclear imaging and allows the target specific tumor visualized by optical imaging. | 45 |
Optical Imaging | AlexaFluor-labeled (ABD)-(ZHER2:342)2-Cys Affibody molecules | BT474, MD-MBA-361,MCF7,and U251 xenogrfts | Initial slope of the curve characterizing the temporal dependence of the fluorescence intensity detected in the tumor depends linearly on HER2 expression | 47 |