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Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology
BACKGROUND: The concept of personalized medicine defines a promising approach in cancer care. High-throughput genomic profiling of tumor specimens allows the identification of actionable mutations that potentially lead to tailored treatment for individuals’ benefit. The aim of this study was to prov...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398177/ https://www.ncbi.nlm.nih.gov/pubmed/30847023 http://dx.doi.org/10.18632/oncotarget.26604 |
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author | Prager, Gerald W. Unseld, Matthias Waneck, Fredrik Mader, Robert Wrba, Fritz Raderer, Markus Fuereder, Thorsten Staber, Phillip Jäger, Ulrich Kieler, Markus Bianconi, Daniela Hoda, Mir Alireza Baumann, Lukas Reinthaller, Alexander Berger, Walter Grimm, Christoph Kölbl, Heinz Sibilia, Maria Müllauer, Leonhard Zielinski, Christoph |
author_facet | Prager, Gerald W. Unseld, Matthias Waneck, Fredrik Mader, Robert Wrba, Fritz Raderer, Markus Fuereder, Thorsten Staber, Phillip Jäger, Ulrich Kieler, Markus Bianconi, Daniela Hoda, Mir Alireza Baumann, Lukas Reinthaller, Alexander Berger, Walter Grimm, Christoph Kölbl, Heinz Sibilia, Maria Müllauer, Leonhard Zielinski, Christoph |
author_sort | Prager, Gerald W. |
collection | PubMed |
description | BACKGROUND: The concept of personalized medicine defines a promising approach in cancer care. High-throughput genomic profiling of tumor specimens allows the identification of actionable mutations that potentially lead to tailored treatment for individuals’ benefit. The aim of this study was to prove efficacy of a personalized treatment option in solid tumor patients after failure of standard treatment concepts. RESULTS: Final analysis demonstrates that 34 patients (62%) had a longer PFS upon experimental treatment (PFS1) when compared to previous therapy (PFS0); PFS ratio > 1.0 (p = 0.002). The median PFS under targeted therapy based on molecular profiling (PFS1) was 112 days (quartiles 66/201) and PFS0 = 61 days (quartiles 51/92; p = 0.002). Of the 55 patients, 31 (56%) showed disease control (DCR), consisting of 2 (4%) patients which achieved a complete remission, 14 (25%) patients with a partial remission and 15 (27%) patients who had a stabilization of disease. Median OS from start of experimental therapy was 348 days (quartiles 177/664). CONCLUSION: The prospective trial EXACT suggests that treatment based on real-time molecular tumor profiling leads to superior clinical benefit. MATERIALS AND METHODS: In this prospective clinical phase II trial, 55 cancer patients, after failure of standard treatment options, aimed to achieve a longer progression-free survival on the experimental treatment based on the individual’s molecular profile (PFS1) when compared to the last treatment given before (PFS0). The personalized medicine approach was conceived to be clinical beneficial for patients who show a PFS ratio (PFS 1/PFS0) of > 1.0. |
format | Online Article Text |
id | pubmed-6398177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-63981772019-03-07 Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology Prager, Gerald W. Unseld, Matthias Waneck, Fredrik Mader, Robert Wrba, Fritz Raderer, Markus Fuereder, Thorsten Staber, Phillip Jäger, Ulrich Kieler, Markus Bianconi, Daniela Hoda, Mir Alireza Baumann, Lukas Reinthaller, Alexander Berger, Walter Grimm, Christoph Kölbl, Heinz Sibilia, Maria Müllauer, Leonhard Zielinski, Christoph Oncotarget Research Paper BACKGROUND: The concept of personalized medicine defines a promising approach in cancer care. High-throughput genomic profiling of tumor specimens allows the identification of actionable mutations that potentially lead to tailored treatment for individuals’ benefit. The aim of this study was to prove efficacy of a personalized treatment option in solid tumor patients after failure of standard treatment concepts. RESULTS: Final analysis demonstrates that 34 patients (62%) had a longer PFS upon experimental treatment (PFS1) when compared to previous therapy (PFS0); PFS ratio > 1.0 (p = 0.002). The median PFS under targeted therapy based on molecular profiling (PFS1) was 112 days (quartiles 66/201) and PFS0 = 61 days (quartiles 51/92; p = 0.002). Of the 55 patients, 31 (56%) showed disease control (DCR), consisting of 2 (4%) patients which achieved a complete remission, 14 (25%) patients with a partial remission and 15 (27%) patients who had a stabilization of disease. Median OS from start of experimental therapy was 348 days (quartiles 177/664). CONCLUSION: The prospective trial EXACT suggests that treatment based on real-time molecular tumor profiling leads to superior clinical benefit. MATERIALS AND METHODS: In this prospective clinical phase II trial, 55 cancer patients, after failure of standard treatment options, aimed to achieve a longer progression-free survival on the experimental treatment based on the individual’s molecular profile (PFS1) when compared to the last treatment given before (PFS0). The personalized medicine approach was conceived to be clinical beneficial for patients who show a PFS ratio (PFS 1/PFS0) of > 1.0. Impact Journals LLC 2019-01-29 /pmc/articles/PMC6398177/ /pubmed/30847023 http://dx.doi.org/10.18632/oncotarget.26604 Text en Copyright: © 2019 Prager et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Prager, Gerald W. Unseld, Matthias Waneck, Fredrik Mader, Robert Wrba, Fritz Raderer, Markus Fuereder, Thorsten Staber, Phillip Jäger, Ulrich Kieler, Markus Bianconi, Daniela Hoda, Mir Alireza Baumann, Lukas Reinthaller, Alexander Berger, Walter Grimm, Christoph Kölbl, Heinz Sibilia, Maria Müllauer, Leonhard Zielinski, Christoph Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology |
title | Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology |
title_full | Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology |
title_fullStr | Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology |
title_full_unstemmed | Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology |
title_short | Results of the extended analysis for cancer treatment (EXACT) trial: a prospective translational study evaluating individualized treatment regimens in oncology |
title_sort | results of the extended analysis for cancer treatment (exact) trial: a prospective translational study evaluating individualized treatment regimens in oncology |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398177/ https://www.ncbi.nlm.nih.gov/pubmed/30847023 http://dx.doi.org/10.18632/oncotarget.26604 |
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