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Contrast Media & Molecular Imaging
Volume 2018, Article ID 7615308, 2 pages

Emergent Techniques for Transporter and Receptor-Based Imaging and Interventional Molecular Imaging

1Institute of Biomedical Sciences, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, RJ, Brazil
2Department of Radiology, Federal University of Rio de Janeiro, 21941-913 Rio de Janeiro, RJ, Brazil
3D’Or Institute for Research and Education, 22281-100 Rio de Janeiro, RJ, Brazil
4Vyripharm Biopharmaceuticals, 77021 Houston, Texas, USA
5Department of Nuclear Medicine, Molecular Imaging and Therapeutic Medicine Research Center, Chonbuk National University Medical School and Hospital, Jeonju, Jeollabuk-do 54896, Republic of Korea
6Research Institute of Clinical Medicine, Biomedical Research Institute, Chonbuk National University Hospital, Chonbuk National University, Jeonju, Jeollabuk-do 54896, Republic of Korea
7Institute for Frontier Science Initiative, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192, Japan
8Brain Research Center, National Yang-Ming University, 11221 Taipei, Taiwan

Correspondence should be addressed to Paulo Henrique Rosado-De-Castro; gro.rodi@odasor.oluap

Received 19 September 2018; Accepted 19 September 2018; Published 20 December 2018

Copyright © 2018 Paulo Henrique Rosado-De-Castro et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

The growing field of molecular imaging has allowed noninvasive in vivo tracking of pharmacological and biological pathways. Translational studies have fast-tracked the application of observations from basic findings to the clinical setting. Amongst the most encouraging methods are transporter and receptor-based imaging, where probes permit the diagnosis of disorders, in addition to the prognostication and evaluation of response to treatments. Precise preoperative staging, surgical preparation, and intraoperative imaging can be achieved using tracers with high sensitivity and specificity. A total of 14 manuscripts were submitted to this special issue, and after rigorous review, 4 were accepted, including one preclinical and three clinical studies.

J. H. Choi et al. created a new approach of radiochemical production via photoactivated reaction to make 18F-labeled PET tracers using small molecular and RGD peptides, which can specifically and strongly bind to integrin αvβ3. Integrin αvβ3 is related to angiogenic endothelial and different tumors, including breast, prostate, lung, and ovarian cancers. In vivo PET imaging after intravenous administration of an 18F-labeled compound to RR1022 sarcoma-bearing Sprague Dawley rats demonstrated a high tumor-to-background ratio, indicating it can be useful for evaluation of tumor angiogenic response.

D. Dai et al. carried out a Phase 2 trial designed to evaluate whether technetium-99m-labeled ethylenedicysteine-glucosamine (99mTc-EC-G) SPECT/CT was noninferior to 18F-labeled fludeoxyglucose (18F-FDG) PET/CT in 17 patients with confirmed nonsmall cell lung cancer (NSCLC). The authors found 100% concordance between both tracers for primary tumor detection and 70% agreement for metastatic tumor detection, indicating that 99mTc-EC-G SPECT/CT may be a clinically useful radiotracer, warranting the preparation of Phase 3 study.

Y. J. Jeong et al. analyzed dopamine transporters (DATs) with 18F-labeled 3-b-(4-iodophenyl)nortropane (FP-CIT) PET on patients with Parkinsonism, cerebellar, and autonomic characteristics in multiple system atrophy with cerebellar ataxia (MSA-C). A total of 49 subjects clinically diagnosed with possible or probable MSA-C were included. The authors found statistically significant differences in postural instability, rigidity, asymmetry, bradykinesia, and specific uptake ratio (SUR) between groups. A subgroup of 22 subjects received dopaminergic medications. Interestingly, all seven subjects with normal exams presented no modification, whereas 10 out of 15 subjects with abnormal exams presented clinical progress.

Finally, D. Dai et al. compared 3D positron emission mammography (PEM) with whole-body PET (WBPET) for patients with breast cancer. A total of 410 women with normal breast, benign tumors, or highly suspicious malignant lesions were randomized at 1 :  1 ratio for imaging with WBPET followed by 3D-PEM or 3D-PEM followed by WBPET. Lumpectomy or mastectomy was carried out on eligible subjects after imaging. The authors reported that 3D-PEM had sensitivity and specificity of 92.8% and 54.5%, respectively, while WBPET had sensitivity and specificity of 95.7% and 56.8%, respectively.

In conclusion, significant developments have been achieved in transporter and receptor-based molecular imaging, and the original articles in this special issue underscore progresses for translation of these promising techniques into the clinic.

Paulo Henrique Rosado-De-Castro
David Yang
Hwan-Jeong Jeong
Kazuma Ogawa
Marcos Fabio Henriques DosSantos
Skye Hsin-Hsien Yeh

Conflicts of Interest

The authors declare that they have no conflicts of interest.