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Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis
BACKGROUND: Tumor protein p63 (p63) has been reported to be highly expressed in giant cell tumor of bone (GCTB). Whether p63 can be treated as a diagnostic marker for GCTB remains unclear. OBJECTIVE: We conducted a meta-analysis to evaluate the applicability of p63 in diagnosing GCTB. DESIGN AND SET...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Paulista de Medicina - APM
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673867/ https://www.ncbi.nlm.nih.gov/pubmed/33111920 http://dx.doi.org/10.1590/1516-3180.2020.0021.R3.24062020 |
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author | Wan, Zihao Lee, Chien-Wei Yuan, Shuai Lee, Oscar Kuang-Shen |
author_facet | Wan, Zihao Lee, Chien-Wei Yuan, Shuai Lee, Oscar Kuang-Shen |
author_sort | Wan, Zihao |
collection | PubMed |
description | BACKGROUND: Tumor protein p63 (p63) has been reported to be highly expressed in giant cell tumor of bone (GCTB). Whether p63 can be treated as a diagnostic marker for GCTB remains unclear. OBJECTIVE: We conducted a meta-analysis to evaluate the applicability of p63 in diagnosing GCTB. DESIGN AND SETTING: Systematic review and meta-analysis carried out in a public hospital, Hong Kong, China. METHODS: We searched PubMed, EMBASE and the Cochrane Library from inception to April 30, 2019. Literature in English or Chinese about the differential diagnosis of GCTB using p63 were included. Animal experiments, reviews, correspondence, case reports, expert opinions and editorials were excluded. Studies were also excluded if they did not provide sufficient information to construct a 2 × 2 contingency table. We calculated individual and pooled sensitivities and specificities. We used I² as an indicator of heterogeneity. RESULTS: Out of 88 records identified, 8 articles on 788 GCTB patients fulfilled the inclusion criteria and were included in the present analysis. Bivariate analyses yielded a pooled mean sensitivity of 0.87 (95% confidence interval, CI, 0.72-0.95) and specificity of 0.71 (95% CI, 0.56-0.82) for using p63 as a biomarker in diagnosing GCTB. The area under the receiver operating characteristic curve was 0.86 (95% CI, 0.82-0.88). CONCLUSION: p63 is a helpful indicator in diagnosing GCTB due to its high sensitivity and specificity. Nonetheless, the results need to be carefully interpreted based on other diagnostic methods such as imaging. SYSTEMATIC REVIEW REGISTRATION: 164115 (PROSPERO registration number) |
format | Online Article Text |
id | pubmed-9673867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Associação Paulista de Medicina - APM |
record_format | MEDLINE/PubMed |
spelling | pubmed-96738672022-11-21 Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis Wan, Zihao Lee, Chien-Wei Yuan, Shuai Lee, Oscar Kuang-Shen Sao Paulo Med J Original Article BACKGROUND: Tumor protein p63 (p63) has been reported to be highly expressed in giant cell tumor of bone (GCTB). Whether p63 can be treated as a diagnostic marker for GCTB remains unclear. OBJECTIVE: We conducted a meta-analysis to evaluate the applicability of p63 in diagnosing GCTB. DESIGN AND SETTING: Systematic review and meta-analysis carried out in a public hospital, Hong Kong, China. METHODS: We searched PubMed, EMBASE and the Cochrane Library from inception to April 30, 2019. Literature in English or Chinese about the differential diagnosis of GCTB using p63 were included. Animal experiments, reviews, correspondence, case reports, expert opinions and editorials were excluded. Studies were also excluded if they did not provide sufficient information to construct a 2 × 2 contingency table. We calculated individual and pooled sensitivities and specificities. We used I² as an indicator of heterogeneity. RESULTS: Out of 88 records identified, 8 articles on 788 GCTB patients fulfilled the inclusion criteria and were included in the present analysis. Bivariate analyses yielded a pooled mean sensitivity of 0.87 (95% confidence interval, CI, 0.72-0.95) and specificity of 0.71 (95% CI, 0.56-0.82) for using p63 as a biomarker in diagnosing GCTB. The area under the receiver operating characteristic curve was 0.86 (95% CI, 0.82-0.88). CONCLUSION: p63 is a helpful indicator in diagnosing GCTB due to its high sensitivity and specificity. Nonetheless, the results need to be carefully interpreted based on other diagnostic methods such as imaging. SYSTEMATIC REVIEW REGISTRATION: 164115 (PROSPERO registration number) Associação Paulista de Medicina - APM 2020-10-20 /pmc/articles/PMC9673867/ /pubmed/33111920 http://dx.doi.org/10.1590/1516-3180.2020.0021.R3.24062020 Text en © 2022 by Associação Paulista de Medicina https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons license. |
spellingShingle | Original Article Wan, Zihao Lee, Chien-Wei Yuan, Shuai Lee, Oscar Kuang-Shen Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis |
title | Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis |
title_full | Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis |
title_fullStr | Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis |
title_full_unstemmed | Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis |
title_short | Can p63 serve as a biomarker for diagnosing giant cell tumor of bone? A systematic review and meta-analysis |
title_sort | can p63 serve as a biomarker for diagnosing giant cell tumor of bone? a systematic review and meta-analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673867/ https://www.ncbi.nlm.nih.gov/pubmed/33111920 http://dx.doi.org/10.1590/1516-3180.2020.0021.R3.24062020 |
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