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Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report
BACKGROUND: Precision medicine based on genomic analysis of germline or tumor tissue is attracting attention. However, there is no consensus on how to apply the results of genomic analysis to treatment. CASE PRESENTATION: A 59-year-old man diagnosed with metastatic prostate cancer was diagnosed with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958728/ https://www.ncbi.nlm.nih.gov/pubmed/31931827 http://dx.doi.org/10.1186/s13000-019-0916-z |
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author | Hongo, Hiroshi Kosaka, Takeo Aimono, Eriko Nishihara, Hiroshi Oya, Mototsugu |
author_facet | Hongo, Hiroshi Kosaka, Takeo Aimono, Eriko Nishihara, Hiroshi Oya, Mototsugu |
author_sort | Hongo, Hiroshi |
collection | PubMed |
description | BACKGROUND: Precision medicine based on genomic analysis of germline or tumor tissue is attracting attention. However, there is no consensus on how to apply the results of genomic analysis to treatment. CASE PRESENTATION: A 59-year-old man diagnosed with metastatic prostate cancer was diagnosed with castration-resistant prostate cancer. Although he was sequentially treated with enzalutamide and abiraterone, bone metastasis progression was identified by skeletal scintigraphy. Therefore, we sequentially performed docetaxel therapy followed by cabazitaxel. After the third cycle of cabazitaxel, his prostate-specific antigen level was stable at < 10 ng/mL, and no radiological progression was detected. The patient’s formalin-fixed paraffin-embedded tumor biopsy specimen underwent multiple-gene testing by next-generation sequencing, which identified a FANCA homodeletion. No significant germline mutation was observed. CONCLUSIONS: We describe a case of aggressive, castration-resistant prostate cancer with FANCA homodeletion. Genomic analysis of prostate cancer tissue can be useful to determine optimal treatment of such cancers. |
format | Online Article Text |
id | pubmed-6958728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69587282020-01-17 Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report Hongo, Hiroshi Kosaka, Takeo Aimono, Eriko Nishihara, Hiroshi Oya, Mototsugu Diagn Pathol Case Report BACKGROUND: Precision medicine based on genomic analysis of germline or tumor tissue is attracting attention. However, there is no consensus on how to apply the results of genomic analysis to treatment. CASE PRESENTATION: A 59-year-old man diagnosed with metastatic prostate cancer was diagnosed with castration-resistant prostate cancer. Although he was sequentially treated with enzalutamide and abiraterone, bone metastasis progression was identified by skeletal scintigraphy. Therefore, we sequentially performed docetaxel therapy followed by cabazitaxel. After the third cycle of cabazitaxel, his prostate-specific antigen level was stable at < 10 ng/mL, and no radiological progression was detected. The patient’s formalin-fixed paraffin-embedded tumor biopsy specimen underwent multiple-gene testing by next-generation sequencing, which identified a FANCA homodeletion. No significant germline mutation was observed. CONCLUSIONS: We describe a case of aggressive, castration-resistant prostate cancer with FANCA homodeletion. Genomic analysis of prostate cancer tissue can be useful to determine optimal treatment of such cancers. BioMed Central 2020-01-13 /pmc/articles/PMC6958728/ /pubmed/31931827 http://dx.doi.org/10.1186/s13000-019-0916-z Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Hongo, Hiroshi Kosaka, Takeo Aimono, Eriko Nishihara, Hiroshi Oya, Mototsugu Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report |
title | Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report |
title_full | Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report |
title_fullStr | Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report |
title_full_unstemmed | Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report |
title_short | Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report |
title_sort | aggressive prostate cancer with somatic loss of the homologous recombination repair gene fanca: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958728/ https://www.ncbi.nlm.nih.gov/pubmed/31931827 http://dx.doi.org/10.1186/s13000-019-0916-z |
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