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Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT

Purpose: To evaluate the value of (18)F-FDG positron emission tomography (PET)/computed tomography (CT) for determining the presence of residual tumors after curettage in patients with endometrial cancer. Methods: Preoperative (18)F-FDG PET/CT was performed in 90 women with endometrial cancer. PET/C...

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Autores principales: Wu, Chunhua, Chen, Ruohua, Zhou, Xiang, Xia, Qian, Liu, Jianjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052915/
https://www.ncbi.nlm.nih.gov/pubmed/32127955
http://dx.doi.org/10.7150/jca.39423
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author Wu, Chunhua
Chen, Ruohua
Zhou, Xiang
Xia, Qian
Liu, Jianjun
author_facet Wu, Chunhua
Chen, Ruohua
Zhou, Xiang
Xia, Qian
Liu, Jianjun
author_sort Wu, Chunhua
collection PubMed
description Purpose: To evaluate the value of (18)F-FDG positron emission tomography (PET)/computed tomography (CT) for determining the presence of residual tumors after curettage in patients with endometrial cancer. Methods: Preoperative (18)F-FDG PET/CT was performed in 90 women with endometrial cancer. PET/CT parameters and clinical characteristics were compared between patients with and without residual tumors. The clinical characteristics of patients with residual tumors that showed low (18)F-FDG uptake were also analyzed. Results: Among the 90 patients, 86 had residual tumors. ROC analysis identified a lesion SUVmax value of 5.0 as the optimal cut-off value for predicting whether or not patients had a residual tumor. With the SUVmax cut-off of 5, the sensitivity, specificity, positive predictive value, and negative predictive values for residual tumor prediction were 87.2%, 100%, 100%, and 26.7%, respectively. Univariate analysis showed significant associations between the high PET group (SUVmax > 5) and low PET group (SUVmax ≤ 5), and histologic type (P = 0.043) and tumor size (P < 0.001) in patients with residual tumors. In patients with low-grade and clear cell carcinomas and a tumor size < 1.35 cm, the probability of being in the low-PET group was 47.6%. In such patients, major parts of the residual tumors showed low (18)F-FDG uptake, similar to that in patients with no residual tumors. Conclusion: SUVmax was the lone predictive value for the presence of residual tumors after curettage in patients with endometrial cancer. Lesion SUVmax greater than 5 suggested a high possibility of residual tumors. In patients with low-grade and clear cell carcinomas with tumor size < 1.35 cm, residual tumors may present low (18)F-FDG uptake, mimicking the metabolic phenotypes of patients without residual tumors.
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spelling pubmed-70529152020-03-03 Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT Wu, Chunhua Chen, Ruohua Zhou, Xiang Xia, Qian Liu, Jianjun J Cancer Research Paper Purpose: To evaluate the value of (18)F-FDG positron emission tomography (PET)/computed tomography (CT) for determining the presence of residual tumors after curettage in patients with endometrial cancer. Methods: Preoperative (18)F-FDG PET/CT was performed in 90 women with endometrial cancer. PET/CT parameters and clinical characteristics were compared between patients with and without residual tumors. The clinical characteristics of patients with residual tumors that showed low (18)F-FDG uptake were also analyzed. Results: Among the 90 patients, 86 had residual tumors. ROC analysis identified a lesion SUVmax value of 5.0 as the optimal cut-off value for predicting whether or not patients had a residual tumor. With the SUVmax cut-off of 5, the sensitivity, specificity, positive predictive value, and negative predictive values for residual tumor prediction were 87.2%, 100%, 100%, and 26.7%, respectively. Univariate analysis showed significant associations between the high PET group (SUVmax > 5) and low PET group (SUVmax ≤ 5), and histologic type (P = 0.043) and tumor size (P < 0.001) in patients with residual tumors. In patients with low-grade and clear cell carcinomas and a tumor size < 1.35 cm, the probability of being in the low-PET group was 47.6%. In such patients, major parts of the residual tumors showed low (18)F-FDG uptake, similar to that in patients with no residual tumors. Conclusion: SUVmax was the lone predictive value for the presence of residual tumors after curettage in patients with endometrial cancer. Lesion SUVmax greater than 5 suggested a high possibility of residual tumors. In patients with low-grade and clear cell carcinomas with tumor size < 1.35 cm, residual tumors may present low (18)F-FDG uptake, mimicking the metabolic phenotypes of patients without residual tumors. Ivyspring International Publisher 2020-02-10 /pmc/articles/PMC7052915/ /pubmed/32127955 http://dx.doi.org/10.7150/jca.39423 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wu, Chunhua
Chen, Ruohua
Zhou, Xiang
Xia, Qian
Liu, Jianjun
Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT
title Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT
title_full Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT
title_fullStr Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT
title_full_unstemmed Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT
title_short Preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)F-FDG PET/CT
title_sort preoperative evaluation of residual tumor in patients with endometrial carcinoma by using (18)f-fdg pet/ct
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052915/
https://www.ncbi.nlm.nih.gov/pubmed/32127955
http://dx.doi.org/10.7150/jca.39423
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