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Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer

BACKGROUND: Malignant pleural effusion (MPE) is a common complication of advanced lung cancer. Research has shown that secreted phosphoprotein-1 (SPP1) is essential in MPE associated with lung cancer. This retrospective study was performed to evaluate the prognostic significance of SPP1 in the MPE o...

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Autores principales: Zhang, He, Liu, Hong-bing, Yuan, Dong-mei, Wang, Zhao-feng, Wang, Yun-fen, Song, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014756/
https://www.ncbi.nlm.nih.gov/pubmed/24758329
http://dx.doi.org/10.1186/1471-2407-14-280
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author Zhang, He
Liu, Hong-bing
Yuan, Dong-mei
Wang, Zhao-feng
Wang, Yun-fen
Song, Yong
author_facet Zhang, He
Liu, Hong-bing
Yuan, Dong-mei
Wang, Zhao-feng
Wang, Yun-fen
Song, Yong
author_sort Zhang, He
collection PubMed
description BACKGROUND: Malignant pleural effusion (MPE) is a common complication of advanced lung cancer. Research has shown that secreted phosphoprotein-1 (SPP1) is essential in MPE associated with lung cancer. This retrospective study was performed to evaluate the prognostic significance of SPP1 in the MPE of patients with non-small cell lung cancer (NSCLC). METHODS: MPE specimens were obtained from 85 NSCLC patients (study group), and pleural effusion specimens were obtained from 24 patients with benign lung disease (control group). Specimens were tested for SPP1 using enzyme-linked immunosorbent assay (ELISA). Based on the cutoff value of receiver operating characteristic (ROC) curve analysis, the study patients were divided into a high-SPP1-expression subgroup and a low-expression subgroup. The primary and secondary endpoints of this study were progression-free survival (PFS) and overall survival (OS). RESULTS: The SPP1 levels of the study group were significantly higher compared to those of the controls (Mann–Whitney U test, P = 0.017). The number of extrapulmonary metastases was significantly higher in the high-SPP1-expressing patients than in the low-expressing patients (P = 0.03). Kaplan-Meier survival analysis showed that SPP1 levels were negatively associated with OS and PFS in both subgroups of study patients (P = 0.026; P = 0.039, respectively). Cox regression analysis showed that SPP1 was an independent prognostic factor in patients with NSCLC (HR = 1.832, 95% confidence interval: 1.003–3.345; P = 0.049). CONCLUSION: SPP1 in pleural effusion can be used for the auxiliary diagnosis of MPE and used to determine the prognosis of patients with NSCLC.
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spelling pubmed-40147562014-05-10 Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer Zhang, He Liu, Hong-bing Yuan, Dong-mei Wang, Zhao-feng Wang, Yun-fen Song, Yong BMC Cancer Research Article BACKGROUND: Malignant pleural effusion (MPE) is a common complication of advanced lung cancer. Research has shown that secreted phosphoprotein-1 (SPP1) is essential in MPE associated with lung cancer. This retrospective study was performed to evaluate the prognostic significance of SPP1 in the MPE of patients with non-small cell lung cancer (NSCLC). METHODS: MPE specimens were obtained from 85 NSCLC patients (study group), and pleural effusion specimens were obtained from 24 patients with benign lung disease (control group). Specimens were tested for SPP1 using enzyme-linked immunosorbent assay (ELISA). Based on the cutoff value of receiver operating characteristic (ROC) curve analysis, the study patients were divided into a high-SPP1-expression subgroup and a low-expression subgroup. The primary and secondary endpoints of this study were progression-free survival (PFS) and overall survival (OS). RESULTS: The SPP1 levels of the study group were significantly higher compared to those of the controls (Mann–Whitney U test, P = 0.017). The number of extrapulmonary metastases was significantly higher in the high-SPP1-expressing patients than in the low-expressing patients (P = 0.03). Kaplan-Meier survival analysis showed that SPP1 levels were negatively associated with OS and PFS in both subgroups of study patients (P = 0.026; P = 0.039, respectively). Cox regression analysis showed that SPP1 was an independent prognostic factor in patients with NSCLC (HR = 1.832, 95% confidence interval: 1.003–3.345; P = 0.049). CONCLUSION: SPP1 in pleural effusion can be used for the auxiliary diagnosis of MPE and used to determine the prognosis of patients with NSCLC. BioMed Central 2014-04-23 /pmc/articles/PMC4014756/ /pubmed/24758329 http://dx.doi.org/10.1186/1471-2407-14-280 Text en Copyright © 2014 Zhang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Zhang, He
Liu, Hong-bing
Yuan, Dong-mei
Wang, Zhao-feng
Wang, Yun-fen
Song, Yong
Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer
title Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer
title_full Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer
title_fullStr Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer
title_full_unstemmed Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer
title_short Prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer
title_sort prognostic value of secreted phosphoprotein-1 in pleural effusion associated with non-small cell lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014756/
https://www.ncbi.nlm.nih.gov/pubmed/24758329
http://dx.doi.org/10.1186/1471-2407-14-280
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