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TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients
We investigated the hypothesis that the varying treatment efficacy of adjuvant 5-fluorouracil (5FU) in stage III colon cancer is linked to the TP53 mutational status. ABCSG-90 was a prospective randomized trial in which effect of adjuvant 5FU was studied in stage III colon cancer patients. Tumor mat...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563117/ https://www.ncbi.nlm.nih.gov/pubmed/26425688 http://dx.doi.org/10.1016/j.ebiom.2015.06.003 |
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author | Kandioler, Daniela Mittlböck, Martina Kappel, Sonja Puhalla, Harald Herbst, Friedrich Langner, Cord Wolf, Brigitte Tschmelitsch, Jörg Schippinger, Walter Steger, Günther Hofbauer, Friedrich Samonigg, Hellmut Gnant, Michael Teleky, Bela Kührer, Irene |
author_facet | Kandioler, Daniela Mittlböck, Martina Kappel, Sonja Puhalla, Harald Herbst, Friedrich Langner, Cord Wolf, Brigitte Tschmelitsch, Jörg Schippinger, Walter Steger, Günther Hofbauer, Friedrich Samonigg, Hellmut Gnant, Michael Teleky, Bela Kührer, Irene |
author_sort | Kandioler, Daniela |
collection | PubMed |
description | We investigated the hypothesis that the varying treatment efficacy of adjuvant 5-fluorouracil (5FU) in stage III colon cancer is linked to the TP53 mutational status. ABCSG-90 was a prospective randomized trial in which effect of adjuvant 5FU was studied in stage III colon cancer patients. Tumor material of 70% of these patients (389/572) was available for analysis of the biomarker TP53 using a TP53-gene-specific Sanger sequencing protocol. Median follow-up was 88 months. TP53 mutation frequency was 33%. A significant interaction between TP53 status, outcomes and nodal category was found (P = 0.0095). In the N1 category, TP53 wildtype patients had significantly better overall survival than TP53 mutated (81.0% vs. 62.0% overall survival at 5 years; HR = 2.131; 95% CI: 1.344–3.378; P = 0.0010). In the N2 category, the TP53 status did not affect survival (P = 0.4992). In TP53 wildtype patients, the prognostic significance of N category was significantly enhanced (P = 0.0002). In TP53 mutated patients, survival curves of N1 and N2 patients overlapped and nodal category was no longer prognostic. The biomarker TP53 independently predicted effect of adjuvant 5FU in N1 colon cancer patients. TP53 was not predictive in N2 patients, in whom 5FU is known to have no effect. |
format | Online Article Text |
id | pubmed-4563117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-45631172015-09-30 TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients Kandioler, Daniela Mittlböck, Martina Kappel, Sonja Puhalla, Harald Herbst, Friedrich Langner, Cord Wolf, Brigitte Tschmelitsch, Jörg Schippinger, Walter Steger, Günther Hofbauer, Friedrich Samonigg, Hellmut Gnant, Michael Teleky, Bela Kührer, Irene EBioMedicine Original Article We investigated the hypothesis that the varying treatment efficacy of adjuvant 5-fluorouracil (5FU) in stage III colon cancer is linked to the TP53 mutational status. ABCSG-90 was a prospective randomized trial in which effect of adjuvant 5FU was studied in stage III colon cancer patients. Tumor material of 70% of these patients (389/572) was available for analysis of the biomarker TP53 using a TP53-gene-specific Sanger sequencing protocol. Median follow-up was 88 months. TP53 mutation frequency was 33%. A significant interaction between TP53 status, outcomes and nodal category was found (P = 0.0095). In the N1 category, TP53 wildtype patients had significantly better overall survival than TP53 mutated (81.0% vs. 62.0% overall survival at 5 years; HR = 2.131; 95% CI: 1.344–3.378; P = 0.0010). In the N2 category, the TP53 status did not affect survival (P = 0.4992). In TP53 wildtype patients, the prognostic significance of N category was significantly enhanced (P = 0.0002). In TP53 mutated patients, survival curves of N1 and N2 patients overlapped and nodal category was no longer prognostic. The biomarker TP53 independently predicted effect of adjuvant 5FU in N1 colon cancer patients. TP53 was not predictive in N2 patients, in whom 5FU is known to have no effect. Elsevier 2015-06-08 /pmc/articles/PMC4563117/ /pubmed/26425688 http://dx.doi.org/10.1016/j.ebiom.2015.06.003 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Kandioler, Daniela Mittlböck, Martina Kappel, Sonja Puhalla, Harald Herbst, Friedrich Langner, Cord Wolf, Brigitte Tschmelitsch, Jörg Schippinger, Walter Steger, Günther Hofbauer, Friedrich Samonigg, Hellmut Gnant, Michael Teleky, Bela Kührer, Irene TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients |
title | TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients |
title_full | TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients |
title_fullStr | TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients |
title_full_unstemmed | TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients |
title_short | TP53 Mutational Status and Prediction of Benefit from Adjuvant 5-Fluorouracil in Stage III Colon Cancer Patients |
title_sort | tp53 mutational status and prediction of benefit from adjuvant 5-fluorouracil in stage iii colon cancer patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563117/ https://www.ncbi.nlm.nih.gov/pubmed/26425688 http://dx.doi.org/10.1016/j.ebiom.2015.06.003 |
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