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Global Translational Medicine                                        Targeted detection in Barrett’s neoplasia



            minimal overlap with WL illumination. By comparison   heterodimer used in the study. Eric J. Seibel is an inventor
            with alternate detection methods, our integrated imaging   on patents filed by the University of Washington on the
            methodology allows for the simultaneous use of both   mmSFE. The remaining authors declare that they have no
            WL and fluorescence imaging. This innovative approach   conflicts of interest.
            enabled  the  identification  of residual  neoplasia  in  a BE
            patient who had undergone an incomplete EMR. This   Author contributions
            technology can also be used to improve visualization   Conceptualization:  Tse-Shao  Chang,  Jing Chen,  Eric J.
            of flat and subtle pre-malignant lesions in BE patients   Seibel, D. Kim Turgeon, Thomas D. Wang
            who are at an increased risk of developing EAC. A larger   Investigation: Tse-Shao Chang, Jing Chen, Richard S. Kwon
            clinical study of 31 human subjects showed that the mean   Data analysis: Tse-Shao Chang, Yang Jiang, Eric J. Seibel
            T/B ratio for Barrett’s neoplasia (HGD and EAC) was   Writing – original draft: Tse-Shao Chang, Thomas D. Wang
            significantly greater than that for non-dysplastic BE, LGD,   Writing – review & editing: Tse-Shao Chang, Thomas D. Wang
            and squamous epithelium.  The T/B ratio was determined
                                 13
            using  a  deep  learning  algorithm.   This  methodological   Ethics approval and consent to participate
                                       17
            advantage provided high levels of sensitivity and specificity   The  research  study  was  approved  by  the  Michigan
            for the detection of Barrett’s neoplasia, thus overcoming   Medicine IRB (HUM00158121) and was registered online
            many shortcomings of conventional detection approaches.
                                                               at ClinicalTrials.gov (NCT03852576). The enrolled subject
              Our findings contribute not only to the expanding   provided written informed consent.
            endoscopic arsenal for the detection of Barrett’s neoplasia but
            also advance targeted detection methods for other imaging   Consent for publication
            methodologies. Peptide heterodimers can also be radiolabeled   Permission  was  obtained  from  the  subject  to  publish
            to stage metastatic Barrett’s neoplasia using positron emission   results.
            tomography-computed tomography to aid in identifying
            optimal treatment strategies for these patients. A  future   Availability of data
            clinical study with a larger number of subjects studied at
            multiple clinical sites can be performed to further validate the   The datasets used and/or analyzed during the current
            initial findings and explore the full potential of this targeted   study are available from the corresponding author upon
            approach for early detection of Barrett’s neoplasia.  reasonable request.

            4. Conclusion                                      References
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            We thank C. Olivo for fabricating the mmSFE and E. Brady      doi: 10.3322/caac.21763
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            This work is supported by the National Institutes of Health      doi: 10.1111/1759-7714.13311
            (CA163059).                                        5.   Shaheen NJ, Falk GW, Iyer PG, Souza RF, Wani S. Guideline
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            Jing Chen and Thomas D. Wang are inventors on patents   2022;117:1177-1180.
            filed by the University of Michigan on the peptide      doi: 10.14309/ajg.0000000000001788



            Volume 3 Issue 2 (2024)                         4                               doi: 10.36922/gtm.2223
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