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• Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected
BACKGROUND: In operable esophageal cancer patients, neoadjuvant therapy benefits only those who respond to the treatment. The • Pancho trial represents the first prospective randomized trial evaluating the relevance of the mark53 status for predicting the effect of two different neoadjuvant chemothe...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290852/ https://www.ncbi.nlm.nih.gov/pubmed/30559831 http://dx.doi.org/10.1007/s10353-018-0527-z |
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author | Kappel-Latif, Sonja Zacherl, Johannes Hejna, Michael Westerhoff, Maria Tamandl, Dietmar Ba-Ssalamah, Ahmed Mittlböck, Martina Wolf, Brigitte Wrba, Friedrich Kührer, Irene Pluschnig, Ursula Schoppmann, Sebastian F. Függer, Reinhold Zwrtek, Ronald Glaser, Karl Karner, Josef Längle, Friedrich Wenzl, Etienne Roka, Rudolf Öfner, Dietmar Tschmelitsch, Jörg Hold, Michael Keil, Felix Gnant, Michael Kandioler, Daniela |
author_facet | Kappel-Latif, Sonja Zacherl, Johannes Hejna, Michael Westerhoff, Maria Tamandl, Dietmar Ba-Ssalamah, Ahmed Mittlböck, Martina Wolf, Brigitte Wrba, Friedrich Kührer, Irene Pluschnig, Ursula Schoppmann, Sebastian F. Függer, Reinhold Zwrtek, Ronald Glaser, Karl Karner, Josef Längle, Friedrich Wenzl, Etienne Roka, Rudolf Öfner, Dietmar Tschmelitsch, Jörg Hold, Michael Keil, Felix Gnant, Michael Kandioler, Daniela |
author_sort | Kappel-Latif, Sonja |
collection | PubMed |
description | BACKGROUND: In operable esophageal cancer patients, neoadjuvant therapy benefits only those who respond to the treatment. The • Pancho trial represents the first prospective randomized trial evaluating the relevance of the mark53 status for predicting the effect of two different neoadjuvant chemotherapies. METHOD: Biomarker analysis was conducted using the mark53 analysis. Calculation of patient number needed was based on a 60% rate of marker positivity, deduced from the results of a phase II pilot study. RESULTS: From 2007–2012, the • Pancho trial recruited 235 patients with operable esophageal cancer in Austria. A total of 181 patients were eligible and could be subjected to mark53 analysis and randomization. After randomizing 74 patients, the overall TP53 mutation rate was 79%. However, due to the high prevalence of marker positivity, the number of projected patients was increased to 181 patients in order to ensure a sufficient number of marker-negative patients. After completion of the trial, the overall TP53 mutation rate was 77.9%. CONCLUSION: Due to high medical need, the recruitment for the academic trial was excellent. Mark53 analysis clearly detected more mutations in the TP53 gene as compared to the cancer-specific p53 literature. Final analysis examining the interaction between the mark53 status and the effect of chemotherapies applied in the • Pancho trial is now awaited. |
format | Online Article Text |
id | pubmed-6290852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-62908522018-12-15 • Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected Kappel-Latif, Sonja Zacherl, Johannes Hejna, Michael Westerhoff, Maria Tamandl, Dietmar Ba-Ssalamah, Ahmed Mittlböck, Martina Wolf, Brigitte Wrba, Friedrich Kührer, Irene Pluschnig, Ursula Schoppmann, Sebastian F. Függer, Reinhold Zwrtek, Ronald Glaser, Karl Karner, Josef Längle, Friedrich Wenzl, Etienne Roka, Rudolf Öfner, Dietmar Tschmelitsch, Jörg Hold, Michael Keil, Felix Gnant, Michael Kandioler, Daniela Eur Surg Short Communication BACKGROUND: In operable esophageal cancer patients, neoadjuvant therapy benefits only those who respond to the treatment. The • Pancho trial represents the first prospective randomized trial evaluating the relevance of the mark53 status for predicting the effect of two different neoadjuvant chemotherapies. METHOD: Biomarker analysis was conducted using the mark53 analysis. Calculation of patient number needed was based on a 60% rate of marker positivity, deduced from the results of a phase II pilot study. RESULTS: From 2007–2012, the • Pancho trial recruited 235 patients with operable esophageal cancer in Austria. A total of 181 patients were eligible and could be subjected to mark53 analysis and randomization. After randomizing 74 patients, the overall TP53 mutation rate was 79%. However, due to the high prevalence of marker positivity, the number of projected patients was increased to 181 patients in order to ensure a sufficient number of marker-negative patients. After completion of the trial, the overall TP53 mutation rate was 77.9%. CONCLUSION: Due to high medical need, the recruitment for the academic trial was excellent. Mark53 analysis clearly detected more mutations in the TP53 gene as compared to the cancer-specific p53 literature. Final analysis examining the interaction between the mark53 status and the effect of chemotherapies applied in the • Pancho trial is now awaited. Springer Vienna 2018-06-11 2018 /pmc/articles/PMC6290852/ /pubmed/30559831 http://dx.doi.org/10.1007/s10353-018-0527-z Text en © The Author(s) 2018 Open Access This 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. |
spellingShingle | Short Communication Kappel-Latif, Sonja Zacherl, Johannes Hejna, Michael Westerhoff, Maria Tamandl, Dietmar Ba-Ssalamah, Ahmed Mittlböck, Martina Wolf, Brigitte Wrba, Friedrich Kührer, Irene Pluschnig, Ursula Schoppmann, Sebastian F. Függer, Reinhold Zwrtek, Ronald Glaser, Karl Karner, Josef Längle, Friedrich Wenzl, Etienne Roka, Rudolf Öfner, Dietmar Tschmelitsch, Jörg Hold, Michael Keil, Felix Gnant, Michael Kandioler, Daniela • Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected |
title | • Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected |
title_full | • Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected |
title_fullStr | • Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected |
title_full_unstemmed | • Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected |
title_short | • Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected |
title_sort | • pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290852/ https://www.ncbi.nlm.nih.gov/pubmed/30559831 http://dx.doi.org/10.1007/s10353-018-0527-z |
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