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Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma
Oral tongue squamous cell carcinoma (OTSCC) is an aggressive cancer associated with poor prognosis. Methods for determining the aggressiveness of OTSCC from analysis of the primary tumour specimen are thus highly desirable. We investigated whether genomic instability and proliferative activity (by m...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567086/ https://www.ncbi.nlm.nih.gov/pubmed/18766188 http://dx.doi.org/10.1038/sj.bjc.6604633 |
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author | Wangsa, D Ryott, M Åvall-Lundqvist, E Petersson, F Elmberger, G Luo, J Ried, T Auer, G Munck-Wikland, E |
author_facet | Wangsa, D Ryott, M Åvall-Lundqvist, E Petersson, F Elmberger, G Luo, J Ried, T Auer, G Munck-Wikland, E |
author_sort | Wangsa, D |
collection | PubMed |
description | Oral tongue squamous cell carcinoma (OTSCC) is an aggressive cancer associated with poor prognosis. Methods for determining the aggressiveness of OTSCC from analysis of the primary tumour specimen are thus highly desirable. We investigated whether genomic instability and proliferative activity (by means of Ki-67 activity) could be of clinical use for prediction of locoregional recurrence in 76 pretreatment OTSCC paraffin samples (stage I, n=22; stage II, n=33; stage III, n=8; stage IV, n=13). Eleven surgical tumour specimens were also analysed for remnants of proliferative activity after preoperative radiotherapy. Ninety-seven percent of cases (n=72) were characterised as being aneuploid as measured by means of image cytometry. Preoperative radiotherapy (50–68 Gy) resulted in significant reduction of proliferative activity in all patients for which post-treatment biopsies were available (P-value=0.001). Proliferative activity was not associated with response to radiation in stage II patients. However, we report a significant correlation between high proliferation rates and locoregional recurrences in stage I OTSCC patients (P-value=0.028). High-proliferative activity is thus related to an elevated risk of recurrence after surgery alone. We therefore conclude that Ki-67 expression level is a potentially useful clinical marker for predicting recurrence in surgically treated stage I OTSCC. |
format | Text |
id | pubmed-2567086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-25670862009-10-07 Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma Wangsa, D Ryott, M Åvall-Lundqvist, E Petersson, F Elmberger, G Luo, J Ried, T Auer, G Munck-Wikland, E Br J Cancer Molecular Diagnostics Oral tongue squamous cell carcinoma (OTSCC) is an aggressive cancer associated with poor prognosis. Methods for determining the aggressiveness of OTSCC from analysis of the primary tumour specimen are thus highly desirable. We investigated whether genomic instability and proliferative activity (by means of Ki-67 activity) could be of clinical use for prediction of locoregional recurrence in 76 pretreatment OTSCC paraffin samples (stage I, n=22; stage II, n=33; stage III, n=8; stage IV, n=13). Eleven surgical tumour specimens were also analysed for remnants of proliferative activity after preoperative radiotherapy. Ninety-seven percent of cases (n=72) were characterised as being aneuploid as measured by means of image cytometry. Preoperative radiotherapy (50–68 Gy) resulted in significant reduction of proliferative activity in all patients for which post-treatment biopsies were available (P-value=0.001). Proliferative activity was not associated with response to radiation in stage II patients. However, we report a significant correlation between high proliferation rates and locoregional recurrences in stage I OTSCC patients (P-value=0.028). High-proliferative activity is thus related to an elevated risk of recurrence after surgery alone. We therefore conclude that Ki-67 expression level is a potentially useful clinical marker for predicting recurrence in surgically treated stage I OTSCC. Nature Publishing Group 2008-10-07 2008-09-02 /pmc/articles/PMC2567086/ /pubmed/18766188 http://dx.doi.org/10.1038/sj.bjc.6604633 Text en Copyright © 2008 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 | Molecular Diagnostics Wangsa, D Ryott, M Åvall-Lundqvist, E Petersson, F Elmberger, G Luo, J Ried, T Auer, G Munck-Wikland, E Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma |
title | Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma |
title_full | Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma |
title_fullStr | Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma |
title_full_unstemmed | Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma |
title_short | Ki-67 expression predicts locoregional recurrence in stage I oral tongue carcinoma |
title_sort | ki-67 expression predicts locoregional recurrence in stage i oral tongue carcinoma |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567086/ https://www.ncbi.nlm.nih.gov/pubmed/18766188 http://dx.doi.org/10.1038/sj.bjc.6604633 |
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