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Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis

Among new biological markers that could become useful prognostic factors for lung carcinoma, Ki-67 is a nuclear protein involved in cell proliferation regulation. Some studies have suggested an association between Ki-67 and poor survival in lung cancer patients. In order to clarify this point, we ha...

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Autores principales: Martin, B, Paesmans, M, Mascaux, C, Berghmans, T, Lothaire, P, Meert, A-P, Lafitte, J-J, Sculier, J-P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409786/
https://www.ncbi.nlm.nih.gov/pubmed/15545971
http://dx.doi.org/10.1038/sj.bjc.6602233
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author Martin, B
Paesmans, M
Mascaux, C
Berghmans, T
Lothaire, P
Meert, A-P
Lafitte, J-J
Sculier, J-P
author_facet Martin, B
Paesmans, M
Mascaux, C
Berghmans, T
Lothaire, P
Meert, A-P
Lafitte, J-J
Sculier, J-P
author_sort Martin, B
collection PubMed
description Among new biological markers that could become useful prognostic factors for lung carcinoma, Ki-67 is a nuclear protein involved in cell proliferation regulation. Some studies have suggested an association between Ki-67 and poor survival in lung cancer patients. In order to clarify this point, we have performed a systematic review of the literature, using the methodology already described by our Group, the European Lung Cancer Working Party. In total, 37 studies, including 3983 patients, were found to be eligible. In total, 49% of the patients were considered as having a tumour positive for the expression of Ki-67 according to the authors cutoff. In all, 29 of the studies dealt with non-small-cell lung carcinoma (NSCLC), one with small-cell carcinoma (SCLC), two with carcinoid tumours and five with any histology. In terms of survival results, Ki-67 was a bad prognosis factor for survival in 15 studies while it was not in 22. As there was no statistical difference in quality scores between the significant and nonsignificant studies evaluable for the meta-analysis, we were allowed to aggregate the survival results. The combined hazard ratio for NSCLC, calculated using a random-effects model was 1.56 (95% CI: 1.30–1.87), showing a worse survival when Ki-67 expression is increased. In conclusion, our meta-analysis shows that the expression of Ki-67 is a factor of poor prognosis for survival in NSCLC.
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spelling pubmed-24097862009-09-10 Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis Martin, B Paesmans, M Mascaux, C Berghmans, T Lothaire, P Meert, A-P Lafitte, J-J Sculier, J-P Br J Cancer Clinical Among new biological markers that could become useful prognostic factors for lung carcinoma, Ki-67 is a nuclear protein involved in cell proliferation regulation. Some studies have suggested an association between Ki-67 and poor survival in lung cancer patients. In order to clarify this point, we have performed a systematic review of the literature, using the methodology already described by our Group, the European Lung Cancer Working Party. In total, 37 studies, including 3983 patients, were found to be eligible. In total, 49% of the patients were considered as having a tumour positive for the expression of Ki-67 according to the authors cutoff. In all, 29 of the studies dealt with non-small-cell lung carcinoma (NSCLC), one with small-cell carcinoma (SCLC), two with carcinoid tumours and five with any histology. In terms of survival results, Ki-67 was a bad prognosis factor for survival in 15 studies while it was not in 22. As there was no statistical difference in quality scores between the significant and nonsignificant studies evaluable for the meta-analysis, we were allowed to aggregate the survival results. The combined hazard ratio for NSCLC, calculated using a random-effects model was 1.56 (95% CI: 1.30–1.87), showing a worse survival when Ki-67 expression is increased. In conclusion, our meta-analysis shows that the expression of Ki-67 is a factor of poor prognosis for survival in NSCLC. Nature Publishing Group 2004-12-13 2004-11-16 /pmc/articles/PMC2409786/ /pubmed/15545971 http://dx.doi.org/10.1038/sj.bjc.6602233 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical
Martin, B
Paesmans, M
Mascaux, C
Berghmans, T
Lothaire, P
Meert, A-P
Lafitte, J-J
Sculier, J-P
Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis
title Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis
title_full Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis
title_fullStr Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis
title_full_unstemmed Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis
title_short Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis
title_sort ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409786/
https://www.ncbi.nlm.nih.gov/pubmed/15545971
http://dx.doi.org/10.1038/sj.bjc.6602233
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