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      Comparison of 68Ga-PSMA-617 PET/CT with mpMRI for the detection of PCa in patients with a PSA level of 4–20 ng/ml before the initial biopsy

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          Abstract

          The study was aimed at assessing the diagnostic performance of 68Ga-PSMA-617 PET/CT in the detection of prostate cancer (PCa) in patients with a prostate-specific antigen (PSA) level of 4–20 ng/ml and to compare its efficacy with that of multiparametric MRI (mpMRI). We analyzed the data of 67 consecutive patients with PSA levels of 4–20 ng/ml who almost simultaneously underwent 68Ga-PSMA-617 PET/CT and mpMRI. 68Ga-PSMA-617 PET/CT and mpMRI diagnostic performances were compared via receiver operating characteristic (ROC) curve analysis. Of the 67 suspected PCa cases, 33 had pathologically confirmed PCa. 68Ga-PSMA-617 PET/CT showed a patient-based sensitivity, specificity, and positive and negative predictive values (PPVs and NPVs) of 87.88%, 88.24%, 87.88%, and 88.24%, respectively. The corresponding values for mpMRI were 84.85%, 52.94%, 63.64%, and 78.26%. The area under the curve values for 68Ga-PSMA-617 PET/CT and mpMRI were 0.881 and 0.689, respectively. 68Ga-PSMA-617 PET/CT showed a better diagnostic performance than mpMRI in the detection of PCa in patients with PSA levels of 4–20 ng/ml.

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          Most cited references27

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          Prostate Cancer, Version 2.2019, NCCN Clinical Practice Guidelines in Oncology

          The NCCN Guidelines for Prostate Cancer include recommendations regarding diagnosis, risk stratification and workup, treatment options for localized disease, and management of recurrent and advanced disease for clinicians who treat patients with prostate cancer. The portions of the guidelines included herein focus on the roles of germline and somatic genetic testing, risk stratification with nomograms and tumor multigene molecular testing, androgen deprivation therapy, secondary hormonal therapy, chemotherapy, and immunotherapy in patients with prostate cancer.
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            Updates in the Eighth Edition of the Tumor-Node-Metastasis Staging Classification for Urologic Cancers

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              N-Myc Drives Neuroendocrine Prostate Cancer Initiated from Human Prostate Epithelial Cells.

              MYCN amplification and overexpression are common in neuroendocrine prostate cancer (NEPC). However, the impact of aberrant N-Myc expression in prostate tumorigenesis and the cellular origin of NEPC have not been established. We define N-Myc and activated AKT1 as oncogenic components sufficient to transform human prostate epithelial cells to prostate adenocarcinoma and NEPC with phenotypic and molecular features of aggressive, late-stage human disease. We directly show that prostate adenocarcinoma and NEPC can arise from a common epithelial clone. Further, N-Myc is required for tumor maintenance, and destabilization of N-Myc through Aurora A kinase inhibition reduces tumor burden. Our findings establish N-Myc as a driver of NEPC and a target for therapeutic intervention.
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                Author and article information

                Contributors
                fmmukf@qq.com
                wangjing@fmmu.edu.cn
                qinwj@fmmu.edu.cn
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                3 July 2020
                3 July 2020
                2020
                : 10
                : 10963
                Affiliations
                [1 ]ISNI 0000 0004 1799 374X, GRID grid.417295.c, Department of Urology, , Xijing Hospital, Fourth Military Medical University, ; 127 West Changle Road, Xi’an, 710032 Shaanxi China
                [2 ]ISNI 0000 0004 1799 374X, GRID grid.417295.c, Department of Nuclear Medicine, , Xijing Hospital, Fourth Military Medical University, ; 127 West Changle Road, Xi’an, 710032 Shaanxi China
                [3 ]ISNI 0000 0004 1799 374X, GRID grid.417295.c, Department of Radiology, , Xijing Hospital, Fourth Military Medical University, ; Xi’an, China
                [4 ]ISNI 0000 0004 1761 4404, GRID grid.233520.5, Department of Immunology, , Fourth Military Medical University, ; Xi’an, China
                [5 ]ISNI 0000 0001 0307 1240, GRID grid.440588.5, Institute of Medical Research, , Northwestern Polytechnical University, ; Xi’an, China
                Article
                67385
                10.1038/s41598-020-67385-9
                7334214
                32620790
                6b78406a-0682-47b2-abab-e2aec793d96b
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 February 2020
                : 2 June 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100007128, Natural Science Foundation of Shaanxi Province;
                Award ID: 2017JM8128
                Funded by: National Natural Science Foundation of China
                Award ID: 81871379
                Award ID: 81372771
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                urological cancer,prostate,cancer imaging
                Uncategorized
                urological cancer, prostate, cancer imaging

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