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Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma
BACKGROUND: Elevated plasma fibrinogen (Fbg) levels contribute to tumor progression and metastasis; however, limited research on Fbg in small cell lung cancer (SCLC) has been conducted. This study evaluated the prognostic value of Fbg levels in patients with SCLC. METHODS: Data on plasma Fbg level,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754299/ https://www.ncbi.nlm.nih.gov/pubmed/29131503 http://dx.doi.org/10.1111/1759-7714.12556 |
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author | Fan, Shanshan Guan, Yin Zhao, Guanfei An, Guangyu |
author_facet | Fan, Shanshan Guan, Yin Zhao, Guanfei An, Guangyu |
author_sort | Fan, Shanshan |
collection | PubMed |
description | BACKGROUND: Elevated plasma fibrinogen (Fbg) levels contribute to tumor progression and metastasis; however, limited research on Fbg in small cell lung cancer (SCLC) has been conducted. This study evaluated the prognostic value of Fbg levels in patients with SCLC. METHODS: Data on plasma Fbg level, clinical features, and overall survival were retrospectively collected. Kaplan–Meier estimates and log‐rank tests were used to analyze the relationship between Fbg level and survival. Multivariate analyses were performed to determine independent prognostic factors. Subgroup analyses were performed based on extensive/limited disease and Eastern Cooperative Oncology Group status. RESULTS: A total of 120 patients with SCLC were included. The one, three, and five‐year survival rates for the entire cohort were 48.3%, 9.2%, and 1.7%, respectively. Univariate analyses revealed that age, alcohol use, clinical stage, pleural effusion, Eastern Cooperative Oncology Group grade, and Fbg and lactate dehydrogenase levels were associated with survival (P < 0.05). The median survival time for patients with high Fbg levels (> 400 mg/dL) was shorter than for those with low Fbg levels (8 vs. 14 months; P = 0.013). Furthermore, multivariate analysis revealed that Fbg was negatively and independently associated with SCLC prognosis (hazard ratio 1.505, 95% confidence interval 1.018–2.226; P = 0.041). Higher Fbg levels were associated with shorter survival in the extensive disease subgroup (7 vs. 12 months; P = 0.004). CONCLUSIONS: Elevated plasma Fbg was an independent factor associated with poor outcomes in SCLC patients and could serve as a prognostic biomarker. |
format | Online Article Text |
id | pubmed-5754299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57542992018-01-09 Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma Fan, Shanshan Guan, Yin Zhao, Guanfei An, Guangyu Thorac Cancer Original Articles BACKGROUND: Elevated plasma fibrinogen (Fbg) levels contribute to tumor progression and metastasis; however, limited research on Fbg in small cell lung cancer (SCLC) has been conducted. This study evaluated the prognostic value of Fbg levels in patients with SCLC. METHODS: Data on plasma Fbg level, clinical features, and overall survival were retrospectively collected. Kaplan–Meier estimates and log‐rank tests were used to analyze the relationship between Fbg level and survival. Multivariate analyses were performed to determine independent prognostic factors. Subgroup analyses were performed based on extensive/limited disease and Eastern Cooperative Oncology Group status. RESULTS: A total of 120 patients with SCLC were included. The one, three, and five‐year survival rates for the entire cohort were 48.3%, 9.2%, and 1.7%, respectively. Univariate analyses revealed that age, alcohol use, clinical stage, pleural effusion, Eastern Cooperative Oncology Group grade, and Fbg and lactate dehydrogenase levels were associated with survival (P < 0.05). The median survival time for patients with high Fbg levels (> 400 mg/dL) was shorter than for those with low Fbg levels (8 vs. 14 months; P = 0.013). Furthermore, multivariate analysis revealed that Fbg was negatively and independently associated with SCLC prognosis (hazard ratio 1.505, 95% confidence interval 1.018–2.226; P = 0.041). Higher Fbg levels were associated with shorter survival in the extensive disease subgroup (7 vs. 12 months; P = 0.004). CONCLUSIONS: Elevated plasma Fbg was an independent factor associated with poor outcomes in SCLC patients and could serve as a prognostic biomarker. John Wiley & Sons Australia, Ltd 2017-11-13 2018-01 /pmc/articles/PMC5754299/ /pubmed/29131503 http://dx.doi.org/10.1111/1759-7714.12556 Text en © 2017 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Fan, Shanshan Guan, Yin Zhao, Guanfei An, Guangyu Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma |
title | Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma |
title_full | Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma |
title_fullStr | Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma |
title_full_unstemmed | Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma |
title_short | Association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma |
title_sort | association between plasma fibrinogen and survival in patients with small‐cell lung carcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754299/ https://www.ncbi.nlm.nih.gov/pubmed/29131503 http://dx.doi.org/10.1111/1759-7714.12556 |
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