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MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis
BACKGROUND: Previous studies on the prognostic role of MUC1 expression in non-small cell lung cancer (NSCLC) remain controversial. We conducted a meta-analysis to appraise the clinicopathological and prognostic effect of MUC1 in NSCLC patients. MATERIALS AND METHODS: Searches of PubMed, EMBASE and C...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685752/ https://www.ncbi.nlm.nih.gov/pubmed/29163831 http://dx.doi.org/10.18632/oncotarget.19861 |
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author | Huang, Xing Sun, Qi Chen, Chen Zhang, Yi Kang, Xin Zhang, Jing-Yuan Ma, Da-Wei Xia, Lei Xu, Lin Xu, Xin-Yu Ren, Bin-Hui |
author_facet | Huang, Xing Sun, Qi Chen, Chen Zhang, Yi Kang, Xin Zhang, Jing-Yuan Ma, Da-Wei Xia, Lei Xu, Lin Xu, Xin-Yu Ren, Bin-Hui |
author_sort | Huang, Xing |
collection | PubMed |
description | BACKGROUND: Previous studies on the prognostic role of MUC1 expression in non-small cell lung cancer (NSCLC) remain controversial. We conducted a meta-analysis to appraise the clinicopathological and prognostic effect of MUC1 in NSCLC patients. MATERIALS AND METHODS: Searches of PubMed, EMBASE and CNKI (Chinese National Knowledge Infrastructure) were conducted and relevant studies were extracted. The pooled hazard ratio (HR) or odds ratio (OR) with 95% confidence intervals (CIs) were used to estimate effects. Heterogeneity among studies and publication bias were also evaluated. RESULTS: A total of 15 studies with 1,682 patients were included in this meta-analysis. The pooled HRs indicated that elevated MUC1 expression was associated with poorer overall survival (HR = 2.12, 95% CI: 1.47–3.05; P < 0.001) and progression-free survival (HR = 2.00, 95% CI: 1.53-2.62; P < 0.001) in patients with NSCLC. Significant associations were also found in patients treated with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) (HR = 3.16, 95% CI: 2.21–4.52, P < 0.001) and with a platinum-based regimen (HR = 4.35, 95% CI: 2.45–7.72, P < 0.001). Additionally, MUC1 overexpression was significantly associated with performance status (OR = 2.32, 95% CI: 1.13–4.73, P = 0.021). CONCLUSIONS: MUC1 could be a valuable biomarker of the prognoses of NSCLC patients. |
format | Online Article Text |
id | pubmed-5685752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56857522017-11-21 MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis Huang, Xing Sun, Qi Chen, Chen Zhang, Yi Kang, Xin Zhang, Jing-Yuan Ma, Da-Wei Xia, Lei Xu, Lin Xu, Xin-Yu Ren, Bin-Hui Oncotarget Meta-Analysis BACKGROUND: Previous studies on the prognostic role of MUC1 expression in non-small cell lung cancer (NSCLC) remain controversial. We conducted a meta-analysis to appraise the clinicopathological and prognostic effect of MUC1 in NSCLC patients. MATERIALS AND METHODS: Searches of PubMed, EMBASE and CNKI (Chinese National Knowledge Infrastructure) were conducted and relevant studies were extracted. The pooled hazard ratio (HR) or odds ratio (OR) with 95% confidence intervals (CIs) were used to estimate effects. Heterogeneity among studies and publication bias were also evaluated. RESULTS: A total of 15 studies with 1,682 patients were included in this meta-analysis. The pooled HRs indicated that elevated MUC1 expression was associated with poorer overall survival (HR = 2.12, 95% CI: 1.47–3.05; P < 0.001) and progression-free survival (HR = 2.00, 95% CI: 1.53-2.62; P < 0.001) in patients with NSCLC. Significant associations were also found in patients treated with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) (HR = 3.16, 95% CI: 2.21–4.52, P < 0.001) and with a platinum-based regimen (HR = 4.35, 95% CI: 2.45–7.72, P < 0.001). Additionally, MUC1 overexpression was significantly associated with performance status (OR = 2.32, 95% CI: 1.13–4.73, P = 0.021). CONCLUSIONS: MUC1 could be a valuable biomarker of the prognoses of NSCLC patients. Impact Journals LLC 2017-08-03 /pmc/articles/PMC5685752/ /pubmed/29163831 http://dx.doi.org/10.18632/oncotarget.19861 Text en Copyright: © 2017 Huang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Huang, Xing Sun, Qi Chen, Chen Zhang, Yi Kang, Xin Zhang, Jing-Yuan Ma, Da-Wei Xia, Lei Xu, Lin Xu, Xin-Yu Ren, Bin-Hui MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis |
title | MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis |
title_full | MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis |
title_fullStr | MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis |
title_full_unstemmed | MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis |
title_short | MUC1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis |
title_sort | muc1 overexpression predicts worse survival in patients with non-small cell lung cancer: evidence from an updated meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685752/ https://www.ncbi.nlm.nih.gov/pubmed/29163831 http://dx.doi.org/10.18632/oncotarget.19861 |
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