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The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan
BACKGROUND: Since June 2019, cancer genomic profiling (CGP) tests have been reimbursed by the National Health Insurance system in Japan, with restrictions for government-designated hospitals with a molecular tumor board composed of multidisciplinary specialists, known as an expert panel (EP). The st...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895780/ https://www.ncbi.nlm.nih.gov/pubmed/33385275 http://dx.doi.org/10.1007/s10147-020-01844-1 |
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author | Sunami, Kuniko Naito, Yoichi Aimono, Eriko Amano, Toraji Ennishi, Daisuke Kage, Hidenori Kanai, Masashi Komine, Keigo Koyama, Takafumi Maeda, Takahiro Morita, Sachi Sakai, Daisuke Kohsaka, Shinji Tsuchihara, Katsuya Yoshino, Takayuki |
author_facet | Sunami, Kuniko Naito, Yoichi Aimono, Eriko Amano, Toraji Ennishi, Daisuke Kage, Hidenori Kanai, Masashi Komine, Keigo Koyama, Takafumi Maeda, Takahiro Morita, Sachi Sakai, Daisuke Kohsaka, Shinji Tsuchihara, Katsuya Yoshino, Takayuki |
author_sort | Sunami, Kuniko |
collection | PubMed |
description | BACKGROUND: Since June 2019, cancer genomic profiling (CGP) tests have been reimbursed by the National Health Insurance system in Japan, with restrictions for government-designated hospitals with a molecular tumor board composed of multidisciplinary specialists, known as an expert panel (EP). The standardization of EPs is a critical challenge for implementing precision oncology in the clinical setting. METHODS: Data on consecutive cases who underwent the CGP tests at 11 core hospitals between June 2019 and January 2020 were collected. We evaluated the proportions of cases that received genomically matched treatments, including investigational new drugs (INDs) based on CGP results, and/or for which genetic counseling was recommended. Two simulated cases were annotated by each EP. The annotated reports were then centrally assessed. RESULTS: Each EP mainly discussed the applicability to genomically matched treatments and the necessity of performing genetic counseling. A pre-review of the report by key members in each EP reportedly made the EP conference more interactive and efficient, and thereby saved time. A total of 747 cases underwent CGP tests, 28 cases (3.7%) received genomically matched treatment, and 17 cases (2.3%) were referred for genetic counseling. Annotated reports for the simulated cases varied across the EPs, particularly the number of recommended IND trials, which seemed to be associated with the actual number of participants in IND trials. CONCLUSIONS: This investigation provides reference data for the application of precision oncology in a clinical setting. Further investigations on the standardization of clinical annotations are warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10147-020-01844-1. |
format | Online Article Text |
id | pubmed-7895780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-78957802021-03-03 The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan Sunami, Kuniko Naito, Yoichi Aimono, Eriko Amano, Toraji Ennishi, Daisuke Kage, Hidenori Kanai, Masashi Komine, Keigo Koyama, Takafumi Maeda, Takahiro Morita, Sachi Sakai, Daisuke Kohsaka, Shinji Tsuchihara, Katsuya Yoshino, Takayuki Int J Clin Oncol Special Article BACKGROUND: Since June 2019, cancer genomic profiling (CGP) tests have been reimbursed by the National Health Insurance system in Japan, with restrictions for government-designated hospitals with a molecular tumor board composed of multidisciplinary specialists, known as an expert panel (EP). The standardization of EPs is a critical challenge for implementing precision oncology in the clinical setting. METHODS: Data on consecutive cases who underwent the CGP tests at 11 core hospitals between June 2019 and January 2020 were collected. We evaluated the proportions of cases that received genomically matched treatments, including investigational new drugs (INDs) based on CGP results, and/or for which genetic counseling was recommended. Two simulated cases were annotated by each EP. The annotated reports were then centrally assessed. RESULTS: Each EP mainly discussed the applicability to genomically matched treatments and the necessity of performing genetic counseling. A pre-review of the report by key members in each EP reportedly made the EP conference more interactive and efficient, and thereby saved time. A total of 747 cases underwent CGP tests, 28 cases (3.7%) received genomically matched treatment, and 17 cases (2.3%) were referred for genetic counseling. Annotated reports for the simulated cases varied across the EPs, particularly the number of recommended IND trials, which seemed to be associated with the actual number of participants in IND trials. CONCLUSIONS: This investigation provides reference data for the application of precision oncology in a clinical setting. Further investigations on the standardization of clinical annotations are warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10147-020-01844-1. Springer Singapore 2021-01-01 2021 /pmc/articles/PMC7895780/ /pubmed/33385275 http://dx.doi.org/10.1007/s10147-020-01844-1 Text en © The Author(s) 2021 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/. |
spellingShingle | Special Article Sunami, Kuniko Naito, Yoichi Aimono, Eriko Amano, Toraji Ennishi, Daisuke Kage, Hidenori Kanai, Masashi Komine, Keigo Koyama, Takafumi Maeda, Takahiro Morita, Sachi Sakai, Daisuke Kohsaka, Shinji Tsuchihara, Katsuya Yoshino, Takayuki The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan |
title | The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan |
title_full | The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan |
title_fullStr | The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan |
title_full_unstemmed | The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan |
title_short | The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan |
title_sort | initial assessment of expert panel performance in core hospitals for cancer genomic medicine in japan |
topic | Special Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895780/ https://www.ncbi.nlm.nih.gov/pubmed/33385275 http://dx.doi.org/10.1007/s10147-020-01844-1 |
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