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Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board
PURPOSE: In 2016, the University of Munich Molecular Tumor Board (MTB) was implemented to initiate a precision oncology program. This review of cases was conducted to assess clinical implications and functionality of the program, to identify current limitations and to inform future directions of the...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261163/ https://www.ncbi.nlm.nih.gov/pubmed/35796778 http://dx.doi.org/10.1007/s00432-022-04165-0 |
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author | Heinrich, Kathrin Miller-Phillips, Lisa Ziemann, Frank Hasselmann, Korbinian Rühlmann, Katharina Flach, Madeleine Biro, Dorottya von Bergwelt-Baildon, Michael Holch, Julian Herold, Tobias von Baumgarten, Louisa Greif, Philipp A. Jeremias, Irmela Wuerstlein, Rachel Casuscelli, Jozefina Spitzweg, Christine Seidensticker, Max Renz, Bernhard Corradini, Stefanie Baumeister, Philipp Goni, Elisabetta Tufman, Amanda Jung, Andreas Kumbrink, Jörg Kirchner, Thomas Klauschen, Frederick Metzeler, Klaus H. Heinemann, Volker Westphalen, C. Benedikt |
author_facet | Heinrich, Kathrin Miller-Phillips, Lisa Ziemann, Frank Hasselmann, Korbinian Rühlmann, Katharina Flach, Madeleine Biro, Dorottya von Bergwelt-Baildon, Michael Holch, Julian Herold, Tobias von Baumgarten, Louisa Greif, Philipp A. Jeremias, Irmela Wuerstlein, Rachel Casuscelli, Jozefina Spitzweg, Christine Seidensticker, Max Renz, Bernhard Corradini, Stefanie Baumeister, Philipp Goni, Elisabetta Tufman, Amanda Jung, Andreas Kumbrink, Jörg Kirchner, Thomas Klauschen, Frederick Metzeler, Klaus H. Heinemann, Volker Westphalen, C. Benedikt |
author_sort | Heinrich, Kathrin |
collection | PubMed |
description | PURPOSE: In 2016, the University of Munich Molecular Tumor Board (MTB) was implemented to initiate a precision oncology program. This review of cases was conducted to assess clinical implications and functionality of the program, to identify current limitations and to inform future directions of these efforts. METHODS: Charts, molecular profiles, and tumor board decisions of the first 1000 consecutive cases (01/2016–03/2020) were reviewed. Descriptive statistics were applied to describe relevant findings. RESULTS: Of the first 1000 patients presented to the MTB; 914 patients received comprehensive genomic profiling. Median age of patients was 56 years and 58% were female. The most prevalent diagnoses were breast (16%) and colorectal cancer (10%). Different types of targeted or genome-wide sequencing assays were used; most of them offered by the local department of pathology. Testing was technically successful in 88%. In 41% of cases, a genomic alteration triggered a therapeutic recommendation. The fraction of patients receiving a tumor board recommendation differed significantly between malignancies ranging from over 50% in breast or biliary tract to less than 30% in pancreatic cancers. Based on a retrospective chart review, 17% of patients with an MTB recommendation received appropriate treatment. CONCLUSION: Based on these retrospective analyses, patients with certain malignancies (breast and biliary tract cancer) tend to be more likely to have actionable variants. The low rate of therapeutic implementation (17% of patients receiving a tumor board recommendation) underscores the importance of meticulous follow-up for these patients and ensuring broad access to innovative therapies for patients receiving molecular tumor profiling. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-04165-0. |
format | Online Article Text |
id | pubmed-9261163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-92611632022-07-07 Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board Heinrich, Kathrin Miller-Phillips, Lisa Ziemann, Frank Hasselmann, Korbinian Rühlmann, Katharina Flach, Madeleine Biro, Dorottya von Bergwelt-Baildon, Michael Holch, Julian Herold, Tobias von Baumgarten, Louisa Greif, Philipp A. Jeremias, Irmela Wuerstlein, Rachel Casuscelli, Jozefina Spitzweg, Christine Seidensticker, Max Renz, Bernhard Corradini, Stefanie Baumeister, Philipp Goni, Elisabetta Tufman, Amanda Jung, Andreas Kumbrink, Jörg Kirchner, Thomas Klauschen, Frederick Metzeler, Klaus H. Heinemann, Volker Westphalen, C. Benedikt J Cancer Res Clin Oncol Original Article – Clinical Oncology PURPOSE: In 2016, the University of Munich Molecular Tumor Board (MTB) was implemented to initiate a precision oncology program. This review of cases was conducted to assess clinical implications and functionality of the program, to identify current limitations and to inform future directions of these efforts. METHODS: Charts, molecular profiles, and tumor board decisions of the first 1000 consecutive cases (01/2016–03/2020) were reviewed. Descriptive statistics were applied to describe relevant findings. RESULTS: Of the first 1000 patients presented to the MTB; 914 patients received comprehensive genomic profiling. Median age of patients was 56 years and 58% were female. The most prevalent diagnoses were breast (16%) and colorectal cancer (10%). Different types of targeted or genome-wide sequencing assays were used; most of them offered by the local department of pathology. Testing was technically successful in 88%. In 41% of cases, a genomic alteration triggered a therapeutic recommendation. The fraction of patients receiving a tumor board recommendation differed significantly between malignancies ranging from over 50% in breast or biliary tract to less than 30% in pancreatic cancers. Based on a retrospective chart review, 17% of patients with an MTB recommendation received appropriate treatment. CONCLUSION: Based on these retrospective analyses, patients with certain malignancies (breast and biliary tract cancer) tend to be more likely to have actionable variants. The low rate of therapeutic implementation (17% of patients receiving a tumor board recommendation) underscores the importance of meticulous follow-up for these patients and ensuring broad access to innovative therapies for patients receiving molecular tumor profiling. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-04165-0. Springer Berlin Heidelberg 2022-07-07 2023 /pmc/articles/PMC9261163/ /pubmed/35796778 http://dx.doi.org/10.1007/s00432-022-04165-0 Text en © The Author(s) 2022, corrected publication 2022 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 | Original Article – Clinical Oncology Heinrich, Kathrin Miller-Phillips, Lisa Ziemann, Frank Hasselmann, Korbinian Rühlmann, Katharina Flach, Madeleine Biro, Dorottya von Bergwelt-Baildon, Michael Holch, Julian Herold, Tobias von Baumgarten, Louisa Greif, Philipp A. Jeremias, Irmela Wuerstlein, Rachel Casuscelli, Jozefina Spitzweg, Christine Seidensticker, Max Renz, Bernhard Corradini, Stefanie Baumeister, Philipp Goni, Elisabetta Tufman, Amanda Jung, Andreas Kumbrink, Jörg Kirchner, Thomas Klauschen, Frederick Metzeler, Klaus H. Heinemann, Volker Westphalen, C. Benedikt Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board |
title | Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board |
title_full | Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board |
title_fullStr | Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board |
title_full_unstemmed | Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board |
title_short | Lessons learned: the first consecutive 1000 patients of the CCCMunich(LMU) Molecular Tumor Board |
title_sort | lessons learned: the first consecutive 1000 patients of the cccmunich(lmu) molecular tumor board |
topic | Original Article – Clinical Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261163/ https://www.ncbi.nlm.nih.gov/pubmed/35796778 http://dx.doi.org/10.1007/s00432-022-04165-0 |
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