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(18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer
The present study aimed to explore the value of fludeoxyglucose F 18 positron emission tomography-computed tomography (PET/CT) for the early prediction of chemotherapy remission rates and survival in patients with recurrent and metastatic breast cancer. A total of 24 patients diagnosed with recurren...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126168/ https://www.ncbi.nlm.nih.gov/pubmed/30214554 http://dx.doi.org/10.3892/ol.2018.9151 |
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author | Zhang, Feng-Chun Xu, Hai-Yan Liu, Jian-Jun Xu, Yuan-Fan Chen, Bin Yang, Yi-Jin Yan, Ning-Ning Song, Shao-Li Lin, Yu-Mei Xu, Ying-Chun |
author_facet | Zhang, Feng-Chun Xu, Hai-Yan Liu, Jian-Jun Xu, Yuan-Fan Chen, Bin Yang, Yi-Jin Yan, Ning-Ning Song, Shao-Li Lin, Yu-Mei Xu, Ying-Chun |
author_sort | Zhang, Feng-Chun |
collection | PubMed |
description | The present study aimed to explore the value of fludeoxyglucose F 18 positron emission tomography-computed tomography (PET/CT) for the early prediction of chemotherapy remission rates and survival in patients with recurrent and metastatic breast cancer. A total of 24 patients diagnosed with recurrent or metastatic breast cancer between 2009 and 2014 were enrolled. All patients underwent a PET/CT examination prior to (PET/CT1) and following (PET/CT2) chemotherapy. Differences of PET/CT1 maximal standardized uptake values (SUV(max)), PET/CT2 SUV(max), ΔSUV(max) and the ΔSUV(max)% between objective remission (OR) and non-OR groups were measured. Survival differences between OR and non-OR groups and the overall survival (OS) between metabolic responsive and metabolic non-responsive groups were analyzed. In the present study, it was revealed that ΔSUV(max) and ΔSUV(max)% were significantly higher in the OR group compared with the non-OR group (P<0.001). Overall survival was significantly prolonged in the OR and metabolic responder groups compared with their respective control groups (P<0.001 and P<0.01, respectively). ΔSUV(max)% were significantly positively associated with OS (r(2)=0.266; P<0.01). In conclusion, PET/CT may be valuable for the early prediction of the chemotherapy efficacy and survival of patients with recurrent or metastatic breast cancer. |
format | Online Article Text |
id | pubmed-6126168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-61261682018-09-13 (18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer Zhang, Feng-Chun Xu, Hai-Yan Liu, Jian-Jun Xu, Yuan-Fan Chen, Bin Yang, Yi-Jin Yan, Ning-Ning Song, Shao-Li Lin, Yu-Mei Xu, Ying-Chun Oncol Lett Articles The present study aimed to explore the value of fludeoxyglucose F 18 positron emission tomography-computed tomography (PET/CT) for the early prediction of chemotherapy remission rates and survival in patients with recurrent and metastatic breast cancer. A total of 24 patients diagnosed with recurrent or metastatic breast cancer between 2009 and 2014 were enrolled. All patients underwent a PET/CT examination prior to (PET/CT1) and following (PET/CT2) chemotherapy. Differences of PET/CT1 maximal standardized uptake values (SUV(max)), PET/CT2 SUV(max), ΔSUV(max) and the ΔSUV(max)% between objective remission (OR) and non-OR groups were measured. Survival differences between OR and non-OR groups and the overall survival (OS) between metabolic responsive and metabolic non-responsive groups were analyzed. In the present study, it was revealed that ΔSUV(max) and ΔSUV(max)% were significantly higher in the OR group compared with the non-OR group (P<0.001). Overall survival was significantly prolonged in the OR and metabolic responder groups compared with their respective control groups (P<0.001 and P<0.01, respectively). ΔSUV(max)% were significantly positively associated with OS (r(2)=0.266; P<0.01). In conclusion, PET/CT may be valuable for the early prediction of the chemotherapy efficacy and survival of patients with recurrent or metastatic breast cancer. D.A. Spandidos 2018-10 2018-07-16 /pmc/articles/PMC6126168/ /pubmed/30214554 http://dx.doi.org/10.3892/ol.2018.9151 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhang, Feng-Chun Xu, Hai-Yan Liu, Jian-Jun Xu, Yuan-Fan Chen, Bin Yang, Yi-Jin Yan, Ning-Ning Song, Shao-Li Lin, Yu-Mei Xu, Ying-Chun (18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer |
title | (18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer |
title_full | (18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer |
title_fullStr | (18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer |
title_full_unstemmed | (18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer |
title_short | (18)F-FDG PET/CT for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer |
title_sort | (18)f-fdg pet/ct for the early prediction of the response rate and survival of patients with recurrent or metastatic breast cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126168/ https://www.ncbi.nlm.nih.gov/pubmed/30214554 http://dx.doi.org/10.3892/ol.2018.9151 |
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