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MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer

AIM: In this study, we aimed to compare the diagnostic values of MRI and FDG-PET for the prediction of the response to neoadjuvant chemoradiotherapy (NACT) of patients with locally advanced Rectal cancer (RC). METHODS: Electronic databases, including PubMed, Embase, and the Cochrane library, were sy...

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Autores principales: Gao, Peng Fei, Lu, Na, Liu, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890074/
https://www.ncbi.nlm.nih.gov/pubmed/36741013
http://dx.doi.org/10.3389/fonc.2023.1031581
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author Gao, Peng Fei
Lu, Na
Liu, Wen
author_facet Gao, Peng Fei
Lu, Na
Liu, Wen
author_sort Gao, Peng Fei
collection PubMed
description AIM: In this study, we aimed to compare the diagnostic values of MRI and FDG-PET for the prediction of the response to neoadjuvant chemoradiotherapy (NACT) of patients with locally advanced Rectal cancer (RC). METHODS: Electronic databases, including PubMed, Embase, and the Cochrane library, were systematically searched through December 2021 for studies that investigated the diagnostic value of MRI and FDG-PET in the prediction of the response of patients with locally advanced RC to NACT. The quality of the included studies was assessed using QUADAS. The pooled sensitivity, specificity, positive and negative likelihood ratio (PLR and NLR), and the area under the ROC (AUC) of MRI and FDG-PET were calculated using a bivariate generalized linear mixed model, random-effects model, and hierarchical regression. RESULTS: A total number of 74 studies with recruited 4,105 locally advanced RC patients were included in this analysis. The pooled sensitivity, specificity, PLR, NLR, and AUC for MRI were 0.83 (95% CI: 0.77–0.88), 0.85 (95% CI: 0.79–0.89), 5.50 (95% CI: 4.11-7.35), 0.20 (95% CI: 0.14–0.27), and 0.91 (95% CI: 0.88–0.93), respectively. The summary sensitivity, specificity, PLR, NLR and AUC for FDG-PET were 0.81 (95% CI: 0.77-0.85), 0.75 (95% CI: 0.70–0.80), 3.29 (95% CI: 2.64–4.10), 0.25 (95% CI: 0.20–0.31), and 0.85 (95% CI: 0.82–0.88), respectively. Moreover, there were no significant differences between MRI and FDG-PET in sensitivity (P = 0.565), and NLR (P = 0.268), while the specificity (P = 0.006), PLR (P = 0.006), and AUC (P = 0.003) of MRI was higher than FDG-PET. CONCLUSIONS: MRI might superior than FGD-PET for the prediction of the response of patients with locally advanced RC to NACT.
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spelling pubmed-98900742023-02-02 MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer Gao, Peng Fei Lu, Na Liu, Wen Front Oncol Oncology AIM: In this study, we aimed to compare the diagnostic values of MRI and FDG-PET for the prediction of the response to neoadjuvant chemoradiotherapy (NACT) of patients with locally advanced Rectal cancer (RC). METHODS: Electronic databases, including PubMed, Embase, and the Cochrane library, were systematically searched through December 2021 for studies that investigated the diagnostic value of MRI and FDG-PET in the prediction of the response of patients with locally advanced RC to NACT. The quality of the included studies was assessed using QUADAS. The pooled sensitivity, specificity, positive and negative likelihood ratio (PLR and NLR), and the area under the ROC (AUC) of MRI and FDG-PET were calculated using a bivariate generalized linear mixed model, random-effects model, and hierarchical regression. RESULTS: A total number of 74 studies with recruited 4,105 locally advanced RC patients were included in this analysis. The pooled sensitivity, specificity, PLR, NLR, and AUC for MRI were 0.83 (95% CI: 0.77–0.88), 0.85 (95% CI: 0.79–0.89), 5.50 (95% CI: 4.11-7.35), 0.20 (95% CI: 0.14–0.27), and 0.91 (95% CI: 0.88–0.93), respectively. The summary sensitivity, specificity, PLR, NLR and AUC for FDG-PET were 0.81 (95% CI: 0.77-0.85), 0.75 (95% CI: 0.70–0.80), 3.29 (95% CI: 2.64–4.10), 0.25 (95% CI: 0.20–0.31), and 0.85 (95% CI: 0.82–0.88), respectively. Moreover, there were no significant differences between MRI and FDG-PET in sensitivity (P = 0.565), and NLR (P = 0.268), while the specificity (P = 0.006), PLR (P = 0.006), and AUC (P = 0.003) of MRI was higher than FDG-PET. CONCLUSIONS: MRI might superior than FGD-PET for the prediction of the response of patients with locally advanced RC to NACT. Frontiers Media S.A. 2023-01-18 /pmc/articles/PMC9890074/ /pubmed/36741013 http://dx.doi.org/10.3389/fonc.2023.1031581 Text en Copyright © 2023 Gao, Lu and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Gao, Peng Fei
Lu, Na
Liu, Wen
MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer
title MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer
title_full MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer
title_fullStr MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer
title_full_unstemmed MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer
title_short MRI VS. FDG-PET for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer
title_sort mri vs. fdg-pet for diagnosis of response to neoadjuvant therapy in patients with locally advanced rectal cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890074/
https://www.ncbi.nlm.nih.gov/pubmed/36741013
http://dx.doi.org/10.3389/fonc.2023.1031581
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