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COT-17 Cancer genomic medicine at Kobe University Hospital
Approximately one year has passed since the Japanese government approved a new plan to fight cancer by promoting the use of genomic medicine in June 2019. Our hospital plays an important role among 6 hospitals to serve cancer genomic medicine for cancer patients in Hyogo Prefecture. Here, we evaluat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699055/ http://dx.doi.org/10.1093/noajnl/vdaa143.100 |
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author | Tanaka, Kazuhiro Toyoda, Masanori Kimbara, Shiro Hashiguchi, Mitsuru Fujita, Yuichi Minami, Hironobu Sasayama, Takashi |
author_facet | Tanaka, Kazuhiro Toyoda, Masanori Kimbara, Shiro Hashiguchi, Mitsuru Fujita, Yuichi Minami, Hironobu Sasayama, Takashi |
author_sort | Tanaka, Kazuhiro |
collection | PubMed |
description | Approximately one year has passed since the Japanese government approved a new plan to fight cancer by promoting the use of genomic medicine in June 2019. Our hospital plays an important role among 6 hospitals to serve cancer genomic medicine for cancer patients in Hyogo Prefecture. Here, we evaluated the system and the current status of cancer genomic medicine in our hospital, and examined future issues and problems. Consecutive 145 patients, who received outpatient treatment for cancer genomic medicine from July 2019 to June 2020 in Kobe University Hospital, were analyzed to examine patients’ background, implementation status, gene profile, and the number of subjects for treatment and clinical trials. The final result of gene profile was obtained in 93 cases, of which 49 cases (52.7%) showed the actionable gene changes to be treated. Six cases of brain tumor were 2 cases of glioblastoma, 2 cases of oligodendroglioma (recurrence), and 2 cases of AT/RT and CNS embryonal tumor. In one case the test was cancelled because Performance Status (PS) of the patient decreased. In another case the actionable gene mutation (PTEN, CDKN2A) was obtained, but the patient lived too far to visit clinical trial site. Almost half of genetic panel tests revealed genomic changes related to treatment, but the number of patients actually targeted for treatment or clinical trials was extremely small. It is necessary to consider the rapid progression of illness and access to facilities conducting clinical trials. |
format | Online Article Text |
id | pubmed-7699055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76990552020-12-02 COT-17 Cancer genomic medicine at Kobe University Hospital Tanaka, Kazuhiro Toyoda, Masanori Kimbara, Shiro Hashiguchi, Mitsuru Fujita, Yuichi Minami, Hironobu Sasayama, Takashi Neurooncol Adv Supplement Abstracts Approximately one year has passed since the Japanese government approved a new plan to fight cancer by promoting the use of genomic medicine in June 2019. Our hospital plays an important role among 6 hospitals to serve cancer genomic medicine for cancer patients in Hyogo Prefecture. Here, we evaluated the system and the current status of cancer genomic medicine in our hospital, and examined future issues and problems. Consecutive 145 patients, who received outpatient treatment for cancer genomic medicine from July 2019 to June 2020 in Kobe University Hospital, were analyzed to examine patients’ background, implementation status, gene profile, and the number of subjects for treatment and clinical trials. The final result of gene profile was obtained in 93 cases, of which 49 cases (52.7%) showed the actionable gene changes to be treated. Six cases of brain tumor were 2 cases of glioblastoma, 2 cases of oligodendroglioma (recurrence), and 2 cases of AT/RT and CNS embryonal tumor. In one case the test was cancelled because Performance Status (PS) of the patient decreased. In another case the actionable gene mutation (PTEN, CDKN2A) was obtained, but the patient lived too far to visit clinical trial site. Almost half of genetic panel tests revealed genomic changes related to treatment, but the number of patients actually targeted for treatment or clinical trials was extremely small. It is necessary to consider the rapid progression of illness and access to facilities conducting clinical trials. Oxford University Press 2020-11-28 /pmc/articles/PMC7699055/ http://dx.doi.org/10.1093/noajnl/vdaa143.100 Text en © The Author(s) 2020. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Supplement Abstracts Tanaka, Kazuhiro Toyoda, Masanori Kimbara, Shiro Hashiguchi, Mitsuru Fujita, Yuichi Minami, Hironobu Sasayama, Takashi COT-17 Cancer genomic medicine at Kobe University Hospital |
title | COT-17 Cancer genomic medicine at Kobe University Hospital |
title_full | COT-17 Cancer genomic medicine at Kobe University Hospital |
title_fullStr | COT-17 Cancer genomic medicine at Kobe University Hospital |
title_full_unstemmed | COT-17 Cancer genomic medicine at Kobe University Hospital |
title_short | COT-17 Cancer genomic medicine at Kobe University Hospital |
title_sort | cot-17 cancer genomic medicine at kobe university hospital |
topic | Supplement Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699055/ http://dx.doi.org/10.1093/noajnl/vdaa143.100 |
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