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NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU
PURPOSE: Comprehensive genomic profiling identifying actionable molecular alterations aims to enable personalized treatment for cancer patients. The purpose of this analysis was to retrospectively assess the impact of personalized recommendations made by a multidisciplinary tumor board (MTB) on the...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053190/ https://www.ncbi.nlm.nih.gov/pubmed/33277683 http://dx.doi.org/10.1007/s00404-020-05881-z |
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author | Sultova, Elena Westphalen, C. Benedikt Jung, Andreas Kumbrink, Joerg Kirchner, Thomas Mayr, Doris Rudelius, Martina Ormanns, Steffen Heinemann, Volker Metzeler, Klaus H. Greif, Philipp A. Burges, Alexander Trillsch, Fabian Mahner, Sven Harbeck, Nadia Wuerstlein, Rachel |
author_facet | Sultova, Elena Westphalen, C. Benedikt Jung, Andreas Kumbrink, Joerg Kirchner, Thomas Mayr, Doris Rudelius, Martina Ormanns, Steffen Heinemann, Volker Metzeler, Klaus H. Greif, Philipp A. Burges, Alexander Trillsch, Fabian Mahner, Sven Harbeck, Nadia Wuerstlein, Rachel |
author_sort | Sultova, Elena |
collection | PubMed |
description | PURPOSE: Comprehensive genomic profiling identifying actionable molecular alterations aims to enable personalized treatment for cancer patients. The purpose of this analysis was to retrospectively assess the impact of personalized recommendations made by a multidisciplinary tumor board (MTB) on the outcome of patients with breast or gynecological cancers, who had progressed under standard treatment. Here, first experiences of our Comprehensive Cancer Center Molecular Tumor Board are reported. METHODS: All patients were part of a prospective local registry. 95 patients diagnosed with metastatic breast cancer or gynecological malignancies underwent extended molecular profiling. From May 2017 through March 2019, the MTB reviewed all clinical cases considering tumor profile and evaluated molecular alterations regarding further diagnostic and therapeutic recommendations. RESULTS: 95 patients with metastatic breast or gynecological cancers were discussed in the MTB (68% breast cancer, 20% ovarian cancer, 5% cervical cancer, 3% endometrial cancer and 4% others). Genes with highest mutation rate were PIK3CA and ERBB2. Overall, 34 patients (36%) received a biomarker-based targeted therapy recommendation. Therapeutic recommendations were implemented in nine cases; four patients experienced clinical benefit with a partial response or disease stabilization lasting over 4 months. CONCLUSION: In the setting of a multidisciplinary molecular tumor board, a small but clinically meaningful group of breast and gynecological cancer patients benefits from comprehensive genomic profiling. Broad and successful implementation of precision medicine is complicated by patient referral at late stage disease and limited access to targeted agents and early clinical trials. TRIAL REGISTRATION NUMBER: 284-10 (03.05.2018). |
format | Online Article Text |
id | pubmed-8053190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80531902021-05-05 NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU Sultova, Elena Westphalen, C. Benedikt Jung, Andreas Kumbrink, Joerg Kirchner, Thomas Mayr, Doris Rudelius, Martina Ormanns, Steffen Heinemann, Volker Metzeler, Klaus H. Greif, Philipp A. Burges, Alexander Trillsch, Fabian Mahner, Sven Harbeck, Nadia Wuerstlein, Rachel Arch Gynecol Obstet Gynecologic Oncology PURPOSE: Comprehensive genomic profiling identifying actionable molecular alterations aims to enable personalized treatment for cancer patients. The purpose of this analysis was to retrospectively assess the impact of personalized recommendations made by a multidisciplinary tumor board (MTB) on the outcome of patients with breast or gynecological cancers, who had progressed under standard treatment. Here, first experiences of our Comprehensive Cancer Center Molecular Tumor Board are reported. METHODS: All patients were part of a prospective local registry. 95 patients diagnosed with metastatic breast cancer or gynecological malignancies underwent extended molecular profiling. From May 2017 through March 2019, the MTB reviewed all clinical cases considering tumor profile and evaluated molecular alterations regarding further diagnostic and therapeutic recommendations. RESULTS: 95 patients with metastatic breast or gynecological cancers were discussed in the MTB (68% breast cancer, 20% ovarian cancer, 5% cervical cancer, 3% endometrial cancer and 4% others). Genes with highest mutation rate were PIK3CA and ERBB2. Overall, 34 patients (36%) received a biomarker-based targeted therapy recommendation. Therapeutic recommendations were implemented in nine cases; four patients experienced clinical benefit with a partial response or disease stabilization lasting over 4 months. CONCLUSION: In the setting of a multidisciplinary molecular tumor board, a small but clinically meaningful group of breast and gynecological cancer patients benefits from comprehensive genomic profiling. Broad and successful implementation of precision medicine is complicated by patient referral at late stage disease and limited access to targeted agents and early clinical trials. TRIAL REGISTRATION NUMBER: 284-10 (03.05.2018). Springer Berlin Heidelberg 2020-12-04 2021 /pmc/articles/PMC8053190/ /pubmed/33277683 http://dx.doi.org/10.1007/s00404-020-05881-z Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Gynecologic Oncology Sultova, Elena Westphalen, C. Benedikt Jung, Andreas Kumbrink, Joerg Kirchner, Thomas Mayr, Doris Rudelius, Martina Ormanns, Steffen Heinemann, Volker Metzeler, Klaus H. Greif, Philipp A. Burges, Alexander Trillsch, Fabian Mahner, Sven Harbeck, Nadia Wuerstlein, Rachel NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU |
title | NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU |
title_full | NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU |
title_fullStr | NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU |
title_full_unstemmed | NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU |
title_short | NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU |
title_sort | ngs-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the ccc munich lmu |
topic | Gynecologic Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053190/ https://www.ncbi.nlm.nih.gov/pubmed/33277683 http://dx.doi.org/10.1007/s00404-020-05881-z |
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