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Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment

PURPOSE: For years, 5-fluorouracil (5-FU) has been the backbone of radiochemotherapy (RCT) of locally advanced rectal cancer. Its main target, thymidylate synthase (TS), is speculated to be an important biomarker for response prediction and long-term prognosis. In this study, we analyzed TS expressi...

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Autores principales: Conradi, Lena-Christin, Bleckmann, Annalen, Schirmer, Markus, Sprenger, Thilo, Jo, Peter, Homayounfar, Kia, Wolff, Hendrik A., Rothe, Hilka, Middel, Peter, Becker, Heinz, Ghadimi, Michael B., Beissbarth, Tim, Liersch, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162628/
https://www.ncbi.nlm.nih.gov/pubmed/21347782
http://dx.doi.org/10.1245/s10434-011-1608-4
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author Conradi, Lena-Christin
Bleckmann, Annalen
Schirmer, Markus
Sprenger, Thilo
Jo, Peter
Homayounfar, Kia
Wolff, Hendrik A.
Rothe, Hilka
Middel, Peter
Becker, Heinz
Ghadimi, Michael B.
Beissbarth, Tim
Liersch, Torsten
author_facet Conradi, Lena-Christin
Bleckmann, Annalen
Schirmer, Markus
Sprenger, Thilo
Jo, Peter
Homayounfar, Kia
Wolff, Hendrik A.
Rothe, Hilka
Middel, Peter
Becker, Heinz
Ghadimi, Michael B.
Beissbarth, Tim
Liersch, Torsten
author_sort Conradi, Lena-Christin
collection PubMed
description PURPOSE: For years, 5-fluorouracil (5-FU) has been the backbone of radiochemotherapy (RCT) of locally advanced rectal cancer. Its main target, thymidylate synthase (TS), is speculated to be an important biomarker for response prediction and long-term prognosis. In this study, we analyzed TS expression in the rectal cancer tissue of 208 patients to evaluate its predictive/prognostic potential. METHODS: All patients included were diagnosed with locally advanced adenocarcinoma of the rectum (UICC II and III) and were treated within randomized clinical trials of the German Rectal Cancer Study Group. Preoperative RCT (50.4 Gy and concomitant either 5-FU or 5-FU and oxaliplatin) was administered in 167 patients followed by surgical resection with total mesorectal excision (TME). Another 41 patients received postoperative RCT. TS levels and further clinicopathological parameters were assessed in univariate and multivariate analyses. Additionally, a TS gene polymorphism was analyzed with respect to the intratumoral protein levels. RESULTS: Low TS expression in pretreatment biopsies correlated with impaired patient survival (p = 0.015). Analysis of a 28-bp repeat revealed a correlation between the *3/*3 genotype and high TS expression in pretherapeutic biopsies. In this study, a correlation of TS expression and grade of RCT-induced tumor regression was not found. Histopathological examination confirmed a complete tumor remission in 16 patients (9.6%). Analyses of the resection specimen indicated an unfavorable prognosis for patients with low intratumoral TS expression in case of detected lymph node metastases (p = 0.04). CONCLUSIONS: TS can serve as a prognostic biomarker indicating an unfavorable prognosis for patients with low TS expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1245/s10434-011-1608-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-31626282011-09-26 Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment Conradi, Lena-Christin Bleckmann, Annalen Schirmer, Markus Sprenger, Thilo Jo, Peter Homayounfar, Kia Wolff, Hendrik A. Rothe, Hilka Middel, Peter Becker, Heinz Ghadimi, Michael B. Beissbarth, Tim Liersch, Torsten Ann Surg Oncol Gastrointestinal Oncology PURPOSE: For years, 5-fluorouracil (5-FU) has been the backbone of radiochemotherapy (RCT) of locally advanced rectal cancer. Its main target, thymidylate synthase (TS), is speculated to be an important biomarker for response prediction and long-term prognosis. In this study, we analyzed TS expression in the rectal cancer tissue of 208 patients to evaluate its predictive/prognostic potential. METHODS: All patients included were diagnosed with locally advanced adenocarcinoma of the rectum (UICC II and III) and were treated within randomized clinical trials of the German Rectal Cancer Study Group. Preoperative RCT (50.4 Gy and concomitant either 5-FU or 5-FU and oxaliplatin) was administered in 167 patients followed by surgical resection with total mesorectal excision (TME). Another 41 patients received postoperative RCT. TS levels and further clinicopathological parameters were assessed in univariate and multivariate analyses. Additionally, a TS gene polymorphism was analyzed with respect to the intratumoral protein levels. RESULTS: Low TS expression in pretreatment biopsies correlated with impaired patient survival (p = 0.015). Analysis of a 28-bp repeat revealed a correlation between the *3/*3 genotype and high TS expression in pretherapeutic biopsies. In this study, a correlation of TS expression and grade of RCT-induced tumor regression was not found. Histopathological examination confirmed a complete tumor remission in 16 patients (9.6%). Analyses of the resection specimen indicated an unfavorable prognosis for patients with low intratumoral TS expression in case of detected lymph node metastases (p = 0.04). CONCLUSIONS: TS can serve as a prognostic biomarker indicating an unfavorable prognosis for patients with low TS expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1245/s10434-011-1608-4) contains supplementary material, which is available to authorized users. Springer-Verlag 2011-02-23 2011 /pmc/articles/PMC3162628/ /pubmed/21347782 http://dx.doi.org/10.1245/s10434-011-1608-4 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Gastrointestinal Oncology
Conradi, Lena-Christin
Bleckmann, Annalen
Schirmer, Markus
Sprenger, Thilo
Jo, Peter
Homayounfar, Kia
Wolff, Hendrik A.
Rothe, Hilka
Middel, Peter
Becker, Heinz
Ghadimi, Michael B.
Beissbarth, Tim
Liersch, Torsten
Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment
title Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment
title_full Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment
title_fullStr Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment
title_full_unstemmed Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment
title_short Thymidylate Synthase as a Prognostic Biomarker for Locally Advanced Rectal Cancer after multimodal Treatment
title_sort thymidylate synthase as a prognostic biomarker for locally advanced rectal cancer after multimodal treatment
topic Gastrointestinal Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162628/
https://www.ncbi.nlm.nih.gov/pubmed/21347782
http://dx.doi.org/10.1245/s10434-011-1608-4
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