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Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study
INTRODUCTION: The purpose of this feasibility study was to select targeted therapies according to “ESMO Scale for Clinical Actionability of molecular Targets (ESCAT)”. Data interpretation was further supported by a browser-based Treatment Decision Support platform (MH Guide, Molecular Health, Heidel...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497348/ https://www.ncbi.nlm.nih.gov/pubmed/37706056 http://dx.doi.org/10.1055/a-2150-9440 |
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author | Jaeger, Bernadette Anna Sophia Krawczyk, Natalia Japp, Anna Sophia Honisch, Ellen Köhrer, Karl Scheuring, Sibylle Petzsch, Patrick Neubauer, Hans Volkmer, Anne Kathrin Esposito, Irene Ruckhäberle, Eugen Niederacher, Dieter Fehm, Tanja |
author_facet | Jaeger, Bernadette Anna Sophia Krawczyk, Natalia Japp, Anna Sophia Honisch, Ellen Köhrer, Karl Scheuring, Sibylle Petzsch, Patrick Neubauer, Hans Volkmer, Anne Kathrin Esposito, Irene Ruckhäberle, Eugen Niederacher, Dieter Fehm, Tanja |
author_sort | Jaeger, Bernadette Anna Sophia |
collection | PubMed |
description | INTRODUCTION: The purpose of this feasibility study was to select targeted therapies according to “ESMO Scale for Clinical Actionability of molecular Targets (ESCAT)”. Data interpretation was further supported by a browser-based Treatment Decision Support platform (MH Guide, Molecular Health, Heidelberg, Germany). PATIENTS: We applied next generation sequencing based whole exome sequencing of tumor tissue and peripheral blood of patients with metastatic breast cancer (n = 44) to detect somatic as well as germline mutations. RESULTS: In 32 metastatic breast cancer patients, data interpretation was feasible. We identified 25 genomic alterations with ESCAT Level of Evidence I or II in 18/32 metastatic breast cancer patients, which were available for evaluation: three copy number gains in HER2 , two g BRCA1 , two g BRCA2 , six PIK3CA, one ESR1 , three PTEN , one AKT1 and two HER2 mutations. In addition, five samples displayed Microsatellite instability high-H. CONCLUSIONS: Resulting treatment options were discussed in a tumor board and could be recommended in a small but relevant proportion of patients with metastatic breast cancer (7/18). Thus, this study is a valuable preliminary work for the establishment of a molecular tumor board within the German initiative “Center for Personalized Medicine” which aims to shorten time for analyses and optimize selection of targeted therapies. |
format | Online Article Text |
id | pubmed-10497348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-104973482023-09-13 Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study Jaeger, Bernadette Anna Sophia Krawczyk, Natalia Japp, Anna Sophia Honisch, Ellen Köhrer, Karl Scheuring, Sibylle Petzsch, Patrick Neubauer, Hans Volkmer, Anne Kathrin Esposito, Irene Ruckhäberle, Eugen Niederacher, Dieter Fehm, Tanja Geburtshilfe Frauenheilkd INTRODUCTION: The purpose of this feasibility study was to select targeted therapies according to “ESMO Scale for Clinical Actionability of molecular Targets (ESCAT)”. Data interpretation was further supported by a browser-based Treatment Decision Support platform (MH Guide, Molecular Health, Heidelberg, Germany). PATIENTS: We applied next generation sequencing based whole exome sequencing of tumor tissue and peripheral blood of patients with metastatic breast cancer (n = 44) to detect somatic as well as germline mutations. RESULTS: In 32 metastatic breast cancer patients, data interpretation was feasible. We identified 25 genomic alterations with ESCAT Level of Evidence I or II in 18/32 metastatic breast cancer patients, which were available for evaluation: three copy number gains in HER2 , two g BRCA1 , two g BRCA2 , six PIK3CA, one ESR1 , three PTEN , one AKT1 and two HER2 mutations. In addition, five samples displayed Microsatellite instability high-H. CONCLUSIONS: Resulting treatment options were discussed in a tumor board and could be recommended in a small but relevant proportion of patients with metastatic breast cancer (7/18). Thus, this study is a valuable preliminary work for the establishment of a molecular tumor board within the German initiative “Center for Personalized Medicine” which aims to shorten time for analyses and optimize selection of targeted therapies. Georg Thieme Verlag KG 2023-09-12 /pmc/articles/PMC10497348/ /pubmed/37706056 http://dx.doi.org/10.1055/a-2150-9440 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Jaeger, Bernadette Anna Sophia Krawczyk, Natalia Japp, Anna Sophia Honisch, Ellen Köhrer, Karl Scheuring, Sibylle Petzsch, Patrick Neubauer, Hans Volkmer, Anne Kathrin Esposito, Irene Ruckhäberle, Eugen Niederacher, Dieter Fehm, Tanja Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study |
title | Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study |
title_full | Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study |
title_fullStr | Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study |
title_full_unstemmed | Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study |
title_short | Whole Exome Analysis to Select Targeted Therapies for Patients with Metastatic Breast Cancer – A Feasibility Study |
title_sort | whole exome analysis to select targeted therapies for patients with metastatic breast cancer – a feasibility study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497348/ https://www.ncbi.nlm.nih.gov/pubmed/37706056 http://dx.doi.org/10.1055/a-2150-9440 |
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