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Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse
Using conventional imaging modalities, it is difficult to detect recurrent lesions in prostate cancer patients who have undergone biochemical relapse, especially in patients with low prostate-specific antigen (PSA) levels. We retrospectively reviewed the files of fifty patients with histopathologica...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427779/ https://www.ncbi.nlm.nih.gov/pubmed/27976632 http://dx.doi.org/10.4103/1008-682X.192638 |
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author | Su, Heng-Chuan Zhu, Yao Ling, Guo-Wen Hu, Si-Long Xu, Xiao-Ping Dai, Bo Ye, Ding-Wei |
author_facet | Su, Heng-Chuan Zhu, Yao Ling, Guo-Wen Hu, Si-Long Xu, Xiao-Ping Dai, Bo Ye, Ding-Wei |
author_sort | Su, Heng-Chuan |
collection | PubMed |
description | Using conventional imaging modalities, it is difficult to detect recurrent lesions in prostate cancer patients who have undergone biochemical relapse, especially in patients with low prostate-specific antigen (PSA) levels. We retrospectively reviewed the files of fifty patients with histopathologically confirmed prostate cancer who underwent (99m)Tc-labeled prostate-specific membrane antigen (PSMA) single-photon emission computed tomography (SPECT)/computed tomography (CT), magnetic resonance imaging (MRI), and bone scan within a 30-day period. PSMA-SPECT/CT indicated metastatic lesions in 39 patients and had a higher detection rate (78.0%) than bone scan (34.0%) or MRI (40.0%). The diagnostic efficiency of PSMA-SPECT/CT imaging for bone and lymph node metastases (50.0% and 42.0%) was better than bone scan (34.0% and 0.0%) or MRI (24.0% and 20.0%). PSMA-SPECT/CT provided a higher detection rate at serum PSA levels of ≤1 ng ml(−1), 1–4 ng ml(−1), 4–10 ng ml(−1), and >10 ng ml(−1). No correlation was found between Gleason score, PSA level, and the tracer tumor/background ratio of metastatic lesions. With the aid of PSMA-SPECT/CT imaging, the therapeutic strategy was changed for 31 patients, and this may have enhanced their clinical outcome. In conclusion, PSMA-SPECT/CT imaging could detect more metastatic lesions and achieve a higher detection rate than conventional imaging modalities at different serum PSA levels in prostate cancer patients who had undergone biochemical relapse. |
format | Online Article Text |
id | pubmed-5427779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54277792017-05-26 Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse Su, Heng-Chuan Zhu, Yao Ling, Guo-Wen Hu, Si-Long Xu, Xiao-Ping Dai, Bo Ye, Ding-Wei Asian J Androl Original Article Using conventional imaging modalities, it is difficult to detect recurrent lesions in prostate cancer patients who have undergone biochemical relapse, especially in patients with low prostate-specific antigen (PSA) levels. We retrospectively reviewed the files of fifty patients with histopathologically confirmed prostate cancer who underwent (99m)Tc-labeled prostate-specific membrane antigen (PSMA) single-photon emission computed tomography (SPECT)/computed tomography (CT), magnetic resonance imaging (MRI), and bone scan within a 30-day period. PSMA-SPECT/CT indicated metastatic lesions in 39 patients and had a higher detection rate (78.0%) than bone scan (34.0%) or MRI (40.0%). The diagnostic efficiency of PSMA-SPECT/CT imaging for bone and lymph node metastases (50.0% and 42.0%) was better than bone scan (34.0% and 0.0%) or MRI (24.0% and 20.0%). PSMA-SPECT/CT provided a higher detection rate at serum PSA levels of ≤1 ng ml(−1), 1–4 ng ml(−1), 4–10 ng ml(−1), and >10 ng ml(−1). No correlation was found between Gleason score, PSA level, and the tracer tumor/background ratio of metastatic lesions. With the aid of PSMA-SPECT/CT imaging, the therapeutic strategy was changed for 31 patients, and this may have enhanced their clinical outcome. In conclusion, PSMA-SPECT/CT imaging could detect more metastatic lesions and achieve a higher detection rate than conventional imaging modalities at different serum PSA levels in prostate cancer patients who had undergone biochemical relapse. Medknow Publications & Media Pvt Ltd 2017 2016-12-13 /pmc/articles/PMC5427779/ /pubmed/27976632 http://dx.doi.org/10.4103/1008-682X.192638 Text en Copyright: © The Author(s)(2017) http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Su, Heng-Chuan Zhu, Yao Ling, Guo-Wen Hu, Si-Long Xu, Xiao-Ping Dai, Bo Ye, Ding-Wei Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse |
title | Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse |
title_full | Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse |
title_fullStr | Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse |
title_full_unstemmed | Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse |
title_short | Evaluation of (99m)Tc-labeled PSMA-SPECT/CT imaging in prostate cancer patients who have undergone biochemical relapse |
title_sort | evaluation of (99m)tc-labeled psma-spect/ct imaging in prostate cancer patients who have undergone biochemical relapse |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427779/ https://www.ncbi.nlm.nih.gov/pubmed/27976632 http://dx.doi.org/10.4103/1008-682X.192638 |
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