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Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy

Objective: We sought to evaluate whether the (18)F-fluorodeoxyglucose uptake normalization of the primary tumor to both the liver and blood pool and lymph nodes to both the liver and blood pool can enhance the discrimination for prognosis prediction in patients with cervical cancer. Methods: A total...

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Autores principales: Chong, Gun Oh, Jeong, Shin Young, Lee, Yoon Hee, Park, Shin-Hyung, Lee, Hyun Jung, Lee, Sang-Woo, Hong, Dae Gy, Lee, Yoon Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355778/
https://www.ncbi.nlm.nih.gov/pubmed/32560143
http://dx.doi.org/10.3390/jcm9061878
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author Chong, Gun Oh
Jeong, Shin Young
Lee, Yoon Hee
Park, Shin-Hyung
Lee, Hyun Jung
Lee, Sang-Woo
Hong, Dae Gy
Lee, Yoon Soon
author_facet Chong, Gun Oh
Jeong, Shin Young
Lee, Yoon Hee
Park, Shin-Hyung
Lee, Hyun Jung
Lee, Sang-Woo
Hong, Dae Gy
Lee, Yoon Soon
author_sort Chong, Gun Oh
collection PubMed
description Objective: We sought to evaluate whether the (18)F-fluorodeoxyglucose uptake normalization of the primary tumor to both the liver and blood pool and lymph nodes to both the liver and blood pool can enhance the discrimination for prognosis prediction in patients with cervical cancer. Methods: A total of 156 patients with cervical cancer (International Federation of Gynecology and Obstetrics stages IIB–IV) treated with concurrent chemoradiotherapy (CCRT) were enrolled. The maximum standardized uptake value (SUV(max)) of tumor (tSUV(max)) and the lymph node (nSUV(max)) divided by the SUV(mean) of the liver (tumor-to-liver ratio (TLR) and node-to-liver (NLR)) and blood pool (tumor-to-blood ratio (TBR) and node-to-blood ratio (NBR)) were investigated. Univariate and multivariate analyses of disease-free survival (DFS) and overall survival (OS) were performed using clinical and metabolic parameters. A receiver operating characteristic curve analysis was performed to compare the accuracy of the metabolic parameters. Results: The multivariate analysis revealed that NLR (hazard ratio ((HR): 3.54; 95% confidence interval (CI): 1.53–8.19; p = 0.0032) and NBR (HR: 3.38; 95% CI: 1.02–11.19; p = 0.0457)) were independent prognostic factors for DFS, while TLR (HR: 4.16; 95% CI: 1.19–14.50; p = 0.0252), TBR (HR: 3.01; 95% CI: 1.04–8.70; p = 0.0415), NLR (HR: 4.84; 95% CI: 1.58–14.81; p = 0.0057), and NBR (HR: 6.87; 95% CI: 1.55–30.54; p = 0.0113) were significant prognostic factors for OS. The normalization of tSUV(max) to the liver or blood pool enhanced the discrimination for prediction of recurrence (tSUV(max) vs. TLR; p = 0.0056 and tSUV(max) vs. TBR; p = 0.0099) and death (tSUV(max) vs. TLR; p < 0.0001 and tSUV(max) vs. TBR; p = 0.0001). Conclusions: The normalization of tSUV(max) was an independent prognostic factor and improved the discrimination for the prediction of tumor recurrence and death in patients with locally advanced cervical cancer treated with CCRT.
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spelling pubmed-73557782020-07-23 Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy Chong, Gun Oh Jeong, Shin Young Lee, Yoon Hee Park, Shin-Hyung Lee, Hyun Jung Lee, Sang-Woo Hong, Dae Gy Lee, Yoon Soon J Clin Med Article Objective: We sought to evaluate whether the (18)F-fluorodeoxyglucose uptake normalization of the primary tumor to both the liver and blood pool and lymph nodes to both the liver and blood pool can enhance the discrimination for prognosis prediction in patients with cervical cancer. Methods: A total of 156 patients with cervical cancer (International Federation of Gynecology and Obstetrics stages IIB–IV) treated with concurrent chemoradiotherapy (CCRT) were enrolled. The maximum standardized uptake value (SUV(max)) of tumor (tSUV(max)) and the lymph node (nSUV(max)) divided by the SUV(mean) of the liver (tumor-to-liver ratio (TLR) and node-to-liver (NLR)) and blood pool (tumor-to-blood ratio (TBR) and node-to-blood ratio (NBR)) were investigated. Univariate and multivariate analyses of disease-free survival (DFS) and overall survival (OS) were performed using clinical and metabolic parameters. A receiver operating characteristic curve analysis was performed to compare the accuracy of the metabolic parameters. Results: The multivariate analysis revealed that NLR (hazard ratio ((HR): 3.54; 95% confidence interval (CI): 1.53–8.19; p = 0.0032) and NBR (HR: 3.38; 95% CI: 1.02–11.19; p = 0.0457)) were independent prognostic factors for DFS, while TLR (HR: 4.16; 95% CI: 1.19–14.50; p = 0.0252), TBR (HR: 3.01; 95% CI: 1.04–8.70; p = 0.0415), NLR (HR: 4.84; 95% CI: 1.58–14.81; p = 0.0057), and NBR (HR: 6.87; 95% CI: 1.55–30.54; p = 0.0113) were significant prognostic factors for OS. The normalization of tSUV(max) to the liver or blood pool enhanced the discrimination for prediction of recurrence (tSUV(max) vs. TLR; p = 0.0056 and tSUV(max) vs. TBR; p = 0.0099) and death (tSUV(max) vs. TLR; p < 0.0001 and tSUV(max) vs. TBR; p = 0.0001). Conclusions: The normalization of tSUV(max) was an independent prognostic factor and improved the discrimination for the prediction of tumor recurrence and death in patients with locally advanced cervical cancer treated with CCRT. MDPI 2020-06-16 /pmc/articles/PMC7355778/ /pubmed/32560143 http://dx.doi.org/10.3390/jcm9061878 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chong, Gun Oh
Jeong, Shin Young
Lee, Yoon Hee
Park, Shin-Hyung
Lee, Hyun Jung
Lee, Sang-Woo
Hong, Dae Gy
Lee, Yoon Soon
Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy
title Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy
title_full Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy
title_fullStr Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy
title_full_unstemmed Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy
title_short Improving the Prognostic Performance of SUV(max) in (18)F-Fluorodeoxyglucose Positron-Emission Tomography/Computed Tomography Using Tumor-to-Liver and Tumor-to-Blood Standard Uptake Ratio for Locally Advanced Cervical Cancer Treated with Concurrent Chemoradiotherapy
title_sort improving the prognostic performance of suv(max) in (18)f-fluorodeoxyglucose positron-emission tomography/computed tomography using tumor-to-liver and tumor-to-blood standard uptake ratio for locally advanced cervical cancer treated with concurrent chemoradiotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355778/
https://www.ncbi.nlm.nih.gov/pubmed/32560143
http://dx.doi.org/10.3390/jcm9061878
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