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Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers

OBJECTIVE: Histological type is important for determining the management of patients with suspicious lung cancers. In this study, PET/CT combined with serum tumor markers were used to evaluate the histological type of lung lesions. MATERIALS AND METHODS: Patients with suspicious lung cancers underwe...

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Autores principales: Jiang, Rifeng, Dong, Ximin, Zhu, Wenzhen, Duan, Qing, Xue, Yunjing, Shen, Yanxia, Zhang, Guopeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587306/
https://www.ncbi.nlm.nih.gov/pubmed/28877268
http://dx.doi.org/10.1371/journal.pone.0184338
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author Jiang, Rifeng
Dong, Ximin
Zhu, Wenzhen
Duan, Qing
Xue, Yunjing
Shen, Yanxia
Zhang, Guopeng
author_facet Jiang, Rifeng
Dong, Ximin
Zhu, Wenzhen
Duan, Qing
Xue, Yunjing
Shen, Yanxia
Zhang, Guopeng
author_sort Jiang, Rifeng
collection PubMed
description OBJECTIVE: Histological type is important for determining the management of patients with suspicious lung cancers. In this study, PET/CT combined with serum tumor markers were used to evaluate the histological type of lung lesions. MATERIALS AND METHODS: Patients with suspicious lung cancers underwent (18)F-FDG PET/CT and serum tumor markers detection. SUVmax of the tumor and serum levels of tumor markers were acquired. Differences in SUVmax and serum levels of tumor markers among different histological types of lung cancers and between EGFR mutation statues of adenocarcinoma were compared. The diagnostic efficiencies of SUVmax alone, each serum tumor marker alone, combined tumor markers and the combination of both methods were further assessed and compared. RESULTS: SCC had the highest level of SUVmax, followed by SCLC and adenocarcinoma, and benign lesions had a lowest level. CYFRA21-1 and SCC-Ag were significantly higher in SCC, NSE was significantly higher in SCLC (P<0.001), and CEA was higher in adenocarcinoma (P = 0.343). The diagnostic efficiencies in evaluating histological types of suspicious lung cancers were insufficient when using each serum tumor marker or SUVmax alone. When combined, the AUC, sensitivity and specificity increased significantly (P<0.05 for all). Additionally, to adenocarcinoma, no significant difference was found between EGFR mutation statuses in SUVmax or serum tumor markers (P>0.05 for all). CONCLUSIONS: SUVmax and serum tumor markers show values in evaluating the histological types of suspicious lung cancers. When properly combined, the diagnostic efficiency can increase significantly.
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spelling pubmed-55873062017-09-15 Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers Jiang, Rifeng Dong, Ximin Zhu, Wenzhen Duan, Qing Xue, Yunjing Shen, Yanxia Zhang, Guopeng PLoS One Research Article OBJECTIVE: Histological type is important for determining the management of patients with suspicious lung cancers. In this study, PET/CT combined with serum tumor markers were used to evaluate the histological type of lung lesions. MATERIALS AND METHODS: Patients with suspicious lung cancers underwent (18)F-FDG PET/CT and serum tumor markers detection. SUVmax of the tumor and serum levels of tumor markers were acquired. Differences in SUVmax and serum levels of tumor markers among different histological types of lung cancers and between EGFR mutation statues of adenocarcinoma were compared. The diagnostic efficiencies of SUVmax alone, each serum tumor marker alone, combined tumor markers and the combination of both methods were further assessed and compared. RESULTS: SCC had the highest level of SUVmax, followed by SCLC and adenocarcinoma, and benign lesions had a lowest level. CYFRA21-1 and SCC-Ag were significantly higher in SCC, NSE was significantly higher in SCLC (P<0.001), and CEA was higher in adenocarcinoma (P = 0.343). The diagnostic efficiencies in evaluating histological types of suspicious lung cancers were insufficient when using each serum tumor marker or SUVmax alone. When combined, the AUC, sensitivity and specificity increased significantly (P<0.05 for all). Additionally, to adenocarcinoma, no significant difference was found between EGFR mutation statuses in SUVmax or serum tumor markers (P>0.05 for all). CONCLUSIONS: SUVmax and serum tumor markers show values in evaluating the histological types of suspicious lung cancers. When properly combined, the diagnostic efficiency can increase significantly. Public Library of Science 2017-09-06 /pmc/articles/PMC5587306/ /pubmed/28877268 http://dx.doi.org/10.1371/journal.pone.0184338 Text en © 2017 Jiang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jiang, Rifeng
Dong, Ximin
Zhu, Wenzhen
Duan, Qing
Xue, Yunjing
Shen, Yanxia
Zhang, Guopeng
Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers
title Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers
title_full Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers
title_fullStr Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers
title_full_unstemmed Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers
title_short Combining PET/CT with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers
title_sort combining pet/ct with serum tumor markers to improve the evaluation of histological type of suspicious lung cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587306/
https://www.ncbi.nlm.nih.gov/pubmed/28877268
http://dx.doi.org/10.1371/journal.pone.0184338
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