Cargando…

Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer

BACKGROUND: Several studies have shown, that circulating tumor cells (CTC) have a negative prognostic value in colorectal cancer patients. Aim of this study was to evaluate the role of CTC in specifically rectal cancer patients regarding the influence on overall survival and to elucidate the impact...

Descripción completa

Detalles Bibliográficos
Autores principales: Hinz, Sebastian, Röder, Christian, Tepel, Jürgen, Hendricks, Alexander, Schafmayer, Clemens, Becker, Thomas, Kalthoff, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682277/
https://www.ncbi.nlm.nih.gov/pubmed/26674974
http://dx.doi.org/10.1186/s12885-015-1989-z
_version_ 1782405872201236480
author Hinz, Sebastian
Röder, Christian
Tepel, Jürgen
Hendricks, Alexander
Schafmayer, Clemens
Becker, Thomas
Kalthoff, Holger
author_facet Hinz, Sebastian
Röder, Christian
Tepel, Jürgen
Hendricks, Alexander
Schafmayer, Clemens
Becker, Thomas
Kalthoff, Holger
author_sort Hinz, Sebastian
collection PubMed
description BACKGROUND: Several studies have shown, that circulating tumor cells (CTC) have a negative prognostic value in colorectal cancer patients. Aim of this study was to evaluate the role of CTC in specifically rectal cancer patients regarding the influence on overall survival and to elucidate the impact of CTC in predicting response after chemoradiation (RCTX). METHODS: In this prospective monocentric study 267 patients with rectal cancer were included. Patients with locally advanced tumors were treated with RCTX followed by surgery. The primary endpoints were: Evaluation of CTC at the time of surgery and correlation with main tumor characteristics, response to neoadjuvant RCTX and overall survival (OS). CTC were detected in the blood using CK20 RT-PCR. RESULTS: Sixty-three patients were treated with neoadjuvant RCTX. In 46.8 % of the patients receiving neoadjuvant RCTX CTC were detected, which was significantly higher than in the group without RCTX (p = 0.002). Histopathologic regression after RCTX was evident in 27.8 % of the patients. In the subgroup of responders after RCTX we found CTC at a significantly lower rate than in non-responders (p = 0.03). No significant association was found between CTC detection and tumor characteristics and OS. The OS was significantly improved for responders compared to non-responders (p = 0.007). CONCLUSIONS: Responders after neoadjuvant RCTX had a lower incidence of CTC compared to non-responders, which might be a result of effective systemic and local treatment prior to surgery. Interestingly, detection of CTC did not correlate with tumor stage and OS, which is in contrast to previous reports of patients with colon cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-015-1989-z) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4682277
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-46822772015-12-18 Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer Hinz, Sebastian Röder, Christian Tepel, Jürgen Hendricks, Alexander Schafmayer, Clemens Becker, Thomas Kalthoff, Holger BMC Cancer Research Article BACKGROUND: Several studies have shown, that circulating tumor cells (CTC) have a negative prognostic value in colorectal cancer patients. Aim of this study was to evaluate the role of CTC in specifically rectal cancer patients regarding the influence on overall survival and to elucidate the impact of CTC in predicting response after chemoradiation (RCTX). METHODS: In this prospective monocentric study 267 patients with rectal cancer were included. Patients with locally advanced tumors were treated with RCTX followed by surgery. The primary endpoints were: Evaluation of CTC at the time of surgery and correlation with main tumor characteristics, response to neoadjuvant RCTX and overall survival (OS). CTC were detected in the blood using CK20 RT-PCR. RESULTS: Sixty-three patients were treated with neoadjuvant RCTX. In 46.8 % of the patients receiving neoadjuvant RCTX CTC were detected, which was significantly higher than in the group without RCTX (p = 0.002). Histopathologic regression after RCTX was evident in 27.8 % of the patients. In the subgroup of responders after RCTX we found CTC at a significantly lower rate than in non-responders (p = 0.03). No significant association was found between CTC detection and tumor characteristics and OS. The OS was significantly improved for responders compared to non-responders (p = 0.007). CONCLUSIONS: Responders after neoadjuvant RCTX had a lower incidence of CTC compared to non-responders, which might be a result of effective systemic and local treatment prior to surgery. Interestingly, detection of CTC did not correlate with tumor stage and OS, which is in contrast to previous reports of patients with colon cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-015-1989-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-16 /pmc/articles/PMC4682277/ /pubmed/26674974 http://dx.doi.org/10.1186/s12885-015-1989-z Text en © Hinz et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hinz, Sebastian
Röder, Christian
Tepel, Jürgen
Hendricks, Alexander
Schafmayer, Clemens
Becker, Thomas
Kalthoff, Holger
Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer
title Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer
title_full Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer
title_fullStr Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer
title_full_unstemmed Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer
title_short Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer
title_sort cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682277/
https://www.ncbi.nlm.nih.gov/pubmed/26674974
http://dx.doi.org/10.1186/s12885-015-1989-z
work_keys_str_mv AT hinzsebastian cytokeratin20positivecirculatingtumorcellsareamarkerforresponseafterneoadjuvantchemoradiationbutnotforprognosisinpatientswithrectalcancer
AT roderchristian cytokeratin20positivecirculatingtumorcellsareamarkerforresponseafterneoadjuvantchemoradiationbutnotforprognosisinpatientswithrectalcancer
AT tepeljurgen cytokeratin20positivecirculatingtumorcellsareamarkerforresponseafterneoadjuvantchemoradiationbutnotforprognosisinpatientswithrectalcancer
AT hendricksalexander cytokeratin20positivecirculatingtumorcellsareamarkerforresponseafterneoadjuvantchemoradiationbutnotforprognosisinpatientswithrectalcancer
AT schafmayerclemens cytokeratin20positivecirculatingtumorcellsareamarkerforresponseafterneoadjuvantchemoradiationbutnotforprognosisinpatientswithrectalcancer
AT beckerthomas cytokeratin20positivecirculatingtumorcellsareamarkerforresponseafterneoadjuvantchemoradiationbutnotforprognosisinpatientswithrectalcancer
AT kalthoffholger cytokeratin20positivecirculatingtumorcellsareamarkerforresponseafterneoadjuvantchemoradiationbutnotforprognosisinpatientswithrectalcancer