Cargando…

High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy

PURPOSE: To investigate the prognostic value of survivin expression in pretreatment specimens from patients with anal cancer treated with concurrent 5-FU and mitomycin C-based chemoradiation (CRT). MATERIAL AND METHODS: Immunohistochemical staining for survivin was performed in pretreatment biopsies...

Descripción completa

Detalles Bibliográficos
Autores principales: Fraunholz, Ingeborg, Rödel, Claus, Distel, Luitpold, Rave-Fränk, Marget, Kohler, Daniela, Falk, Stefan, Rödel, Franz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430559/
https://www.ncbi.nlm.nih.gov/pubmed/22697293
http://dx.doi.org/10.1186/1748-717X-7-88
_version_ 1782241950499340288
author Fraunholz, Ingeborg
Rödel, Claus
Distel, Luitpold
Rave-Fränk, Marget
Kohler, Daniela
Falk, Stefan
Rödel, Franz
author_facet Fraunholz, Ingeborg
Rödel, Claus
Distel, Luitpold
Rave-Fränk, Marget
Kohler, Daniela
Falk, Stefan
Rödel, Franz
author_sort Fraunholz, Ingeborg
collection PubMed
description PURPOSE: To investigate the prognostic value of survivin expression in pretreatment specimens from patients with anal cancer treated with concurrent 5-FU and mitomycin C-based chemoradiation (CRT). MATERIAL AND METHODS: Immunohistochemical staining for survivin was performed in pretreatment biopsies of 62 patients with anal carcinoma. Survivin expression was correlated with clinical and histopathological characteristics as well as local failure free- (LFFS), distant metastases free- (DMFS), cancer specific- (CSS), and overall survival (OS). RESULTS: Survivin staining intensity was weak in 10%, intermediate in 48% and intense in 42% of the patients. No association between survivin expression and clinicopathologic factors (tumor stage, age and HIV status) could be shown. In univariate analysis, the level of survivin staining was significantly correlated with DMFS (low survivin vs. high survivin: 94% vs. 74%, p = 0.04). T-stage, N-stage and the tumor grading were significantly associated with OS and CSS and with DMFS and LFFS, respectively. In multivariate analysis, survivin was confirmed as independent prognostic parameter for DMFS (RR, 0.04; p = 0.02) and for OS (RR, 0.27; p = 0.04). CONCLUSION: Our results demonstrated that the level of pretreatment survivin is correlated with the clinical outcome in patients with anal carcinoma treated with concurrent CRT. Further studies are warranted to elucidate the complex role of survivin for the oncologic treatment and to exploit the protein as a therapeutic target in combined modality treatment of anal cancer.
format Online
Article
Text
id pubmed-3430559
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-34305592012-08-30 High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy Fraunholz, Ingeborg Rödel, Claus Distel, Luitpold Rave-Fränk, Marget Kohler, Daniela Falk, Stefan Rödel, Franz Radiat Oncol Research PURPOSE: To investigate the prognostic value of survivin expression in pretreatment specimens from patients with anal cancer treated with concurrent 5-FU and mitomycin C-based chemoradiation (CRT). MATERIAL AND METHODS: Immunohistochemical staining for survivin was performed in pretreatment biopsies of 62 patients with anal carcinoma. Survivin expression was correlated with clinical and histopathological characteristics as well as local failure free- (LFFS), distant metastases free- (DMFS), cancer specific- (CSS), and overall survival (OS). RESULTS: Survivin staining intensity was weak in 10%, intermediate in 48% and intense in 42% of the patients. No association between survivin expression and clinicopathologic factors (tumor stage, age and HIV status) could be shown. In univariate analysis, the level of survivin staining was significantly correlated with DMFS (low survivin vs. high survivin: 94% vs. 74%, p = 0.04). T-stage, N-stage and the tumor grading were significantly associated with OS and CSS and with DMFS and LFFS, respectively. In multivariate analysis, survivin was confirmed as independent prognostic parameter for DMFS (RR, 0.04; p = 0.02) and for OS (RR, 0.27; p = 0.04). CONCLUSION: Our results demonstrated that the level of pretreatment survivin is correlated with the clinical outcome in patients with anal carcinoma treated with concurrent CRT. Further studies are warranted to elucidate the complex role of survivin for the oncologic treatment and to exploit the protein as a therapeutic target in combined modality treatment of anal cancer. BioMed Central 2012-06-14 /pmc/articles/PMC3430559/ /pubmed/22697293 http://dx.doi.org/10.1186/1748-717X-7-88 Text en Copyright ©2012 Fraunholz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Fraunholz, Ingeborg
Rödel, Claus
Distel, Luitpold
Rave-Fränk, Marget
Kohler, Daniela
Falk, Stefan
Rödel, Franz
High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
title High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
title_full High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
title_fullStr High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
title_full_unstemmed High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
title_short High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
title_sort high survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430559/
https://www.ncbi.nlm.nih.gov/pubmed/22697293
http://dx.doi.org/10.1186/1748-717X-7-88
work_keys_str_mv AT fraunholzingeborg highsurvivinexpressionasariskfactorinpatientswithanalcarcinomatreatedwithconcurrentchemoradiotherapy
AT rodelclaus highsurvivinexpressionasariskfactorinpatientswithanalcarcinomatreatedwithconcurrentchemoradiotherapy
AT distelluitpold highsurvivinexpressionasariskfactorinpatientswithanalcarcinomatreatedwithconcurrentchemoradiotherapy
AT ravefrankmarget highsurvivinexpressionasariskfactorinpatientswithanalcarcinomatreatedwithconcurrentchemoradiotherapy
AT kohlerdaniela highsurvivinexpressionasariskfactorinpatientswithanalcarcinomatreatedwithconcurrentchemoradiotherapy
AT falkstefan highsurvivinexpressionasariskfactorinpatientswithanalcarcinomatreatedwithconcurrentchemoradiotherapy
AT rodelfranz highsurvivinexpressionasariskfactorinpatientswithanalcarcinomatreatedwithconcurrentchemoradiotherapy