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Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis
BACKGROUND: Many studies have evaluated the relationship between alkaline phosphatase (ALP) and the prognosis for prostate cancer (PCa). But they have not reached a widespread consensus yet. Therefore, we completed a meta-analysis to ascertain the significance of ALP and the prognosis for PCa. METHO...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124801/ https://www.ncbi.nlm.nih.gov/pubmed/30214305 http://dx.doi.org/10.2147/CMAR.S174237 |
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author | Li, Dongyang Lv, Hang Hao, Xuanyu Hu, Bin Song, Yongsheng |
author_facet | Li, Dongyang Lv, Hang Hao, Xuanyu Hu, Bin Song, Yongsheng |
author_sort | Li, Dongyang |
collection | PubMed |
description | BACKGROUND: Many studies have evaluated the relationship between alkaline phosphatase (ALP) and the prognosis for prostate cancer (PCa). But they have not reached a widespread consensus yet. Therefore, we completed a meta-analysis to ascertain the significance of ALP and the prognosis for PCa. METHODS: A literature search was performed in the PubMed, Embase, and Web of Science databases. HRs concerning overall survival (OS), progression-free survival (PFS), and cancer-specific survival (CSS) were extracted to evaluate the impacts of ALP on the prognosis for PCa. Subgroup analyses were conducted on different study types, regions, sample sizes, and cutoff values. Sensitivity analysis was performed by removing one study in sequence. RESULTS: A total of 63 studies from 54 articles with 16,135 patients were included in this meta-analysis. The pooled results indicated that high baseline ALP was associated with obviously poor OS (HR=1.74, 95% CI: 1.47–2.06) and PFS (HR=1.60, 95% CI: 1.13–2.26) in patients with PCa. The pooled HR for bone-specific ALP and OS was 1.76 (95% CI: 1.45–2.15). However, no association between ALP and CSS (HR=1.002, 95% CI: 0.998–1.005) was found for PCa. The results of subgroup analyses were all in accordance with the main findings. Sensitivity analysis suggested that no single study could affect the stability of the results. CONCLUSION: High serum ALP is significantly associated with poor OS and PFS except for CSS in PCa. ALP is an efficient and convenient biomarker for PCa prognosis. |
format | Online Article Text |
id | pubmed-6124801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61248012018-09-13 Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis Li, Dongyang Lv, Hang Hao, Xuanyu Hu, Bin Song, Yongsheng Cancer Manag Res Original Research BACKGROUND: Many studies have evaluated the relationship between alkaline phosphatase (ALP) and the prognosis for prostate cancer (PCa). But they have not reached a widespread consensus yet. Therefore, we completed a meta-analysis to ascertain the significance of ALP and the prognosis for PCa. METHODS: A literature search was performed in the PubMed, Embase, and Web of Science databases. HRs concerning overall survival (OS), progression-free survival (PFS), and cancer-specific survival (CSS) were extracted to evaluate the impacts of ALP on the prognosis for PCa. Subgroup analyses were conducted on different study types, regions, sample sizes, and cutoff values. Sensitivity analysis was performed by removing one study in sequence. RESULTS: A total of 63 studies from 54 articles with 16,135 patients were included in this meta-analysis. The pooled results indicated that high baseline ALP was associated with obviously poor OS (HR=1.74, 95% CI: 1.47–2.06) and PFS (HR=1.60, 95% CI: 1.13–2.26) in patients with PCa. The pooled HR for bone-specific ALP and OS was 1.76 (95% CI: 1.45–2.15). However, no association between ALP and CSS (HR=1.002, 95% CI: 0.998–1.005) was found for PCa. The results of subgroup analyses were all in accordance with the main findings. Sensitivity analysis suggested that no single study could affect the stability of the results. CONCLUSION: High serum ALP is significantly associated with poor OS and PFS except for CSS in PCa. ALP is an efficient and convenient biomarker for PCa prognosis. Dove Medical Press 2018-08-30 /pmc/articles/PMC6124801/ /pubmed/30214305 http://dx.doi.org/10.2147/CMAR.S174237 Text en © 2018 Li et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Li, Dongyang Lv, Hang Hao, Xuanyu Hu, Bin Song, Yongsheng Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis |
title | Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis |
title_full | Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis |
title_fullStr | Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis |
title_full_unstemmed | Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis |
title_short | Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis |
title_sort | prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124801/ https://www.ncbi.nlm.nih.gov/pubmed/30214305 http://dx.doi.org/10.2147/CMAR.S174237 |
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