Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report

Abstract 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 diagnos...

Full description

Bibliographic Details
Main Authors: Hiroshi Hongo, Takeo Kosaka, Eriko Aimono, Hiroshi Nishihara, Mototsugu Oya
Format: Article
Language:English
Published: BMC 2020-01-01
Series:Diagnostic Pathology
Subjects:
Online Access:https://doi.org/10.1186/s13000-019-0916-z
id doaj-e34530f1af0e439898e0b4712f6a85bd
record_format Article
spelling doaj-e34530f1af0e439898e0b4712f6a85bd2021-01-17T12:23:36ZengBMCDiagnostic Pathology1746-15962020-01-011511410.1186/s13000-019-0916-zAggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case reportHiroshi Hongo0Takeo Kosaka1Eriko Aimono2Hiroshi Nishihara3Mototsugu Oya4Department of Urology, Keio University School of MedicineDepartment of Urology, Keio University School of MedicineGenomics Unit, Keio Cancer Center, Keio University School of MedicineGenomics Unit, Keio Cancer Center, Keio University School of MedicineDepartment of Urology, Keio University School of MedicineAbstract 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.https://doi.org/10.1186/s13000-019-0916-zFANCAHomologous recombination repairCastration-resistant prostate cancerNext-generation sequencingGenomic analysis
collection DOAJ
language English
format Article
sources DOAJ
author Hiroshi Hongo
Takeo Kosaka
Eriko Aimono
Hiroshi Nishihara
Mototsugu Oya
spellingShingle Hiroshi Hongo
Takeo Kosaka
Eriko Aimono
Hiroshi Nishihara
Mototsugu Oya
Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report
Diagnostic Pathology
FANCA
Homologous recombination repair
Castration-resistant prostate cancer
Next-generation sequencing
Genomic analysis
author_facet Hiroshi Hongo
Takeo Kosaka
Eriko Aimono
Hiroshi Nishihara
Mototsugu Oya
author_sort Hiroshi Hongo
title 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_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_sort aggressive prostate cancer with somatic loss of the homologous recombination repair gene fanca: a case report
publisher BMC
series Diagnostic Pathology
issn 1746-1596
publishDate 2020-01-01
description Abstract 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.
topic FANCA
Homologous recombination repair
Castration-resistant prostate cancer
Next-generation sequencing
Genomic analysis
url https://doi.org/10.1186/s13000-019-0916-z
work_keys_str_mv AT hiroshihongo aggressiveprostatecancerwithsomaticlossofthehomologousrecombinationrepairgenefancaacasereport
AT takeokosaka aggressiveprostatecancerwithsomaticlossofthehomologousrecombinationrepairgenefancaacasereport
AT erikoaimono aggressiveprostatecancerwithsomaticlossofthehomologousrecombinationrepairgenefancaacasereport
AT hiroshinishihara aggressiveprostatecancerwithsomaticlossofthehomologousrecombinationrepairgenefancaacasereport
AT mototsuguoya aggressiveprostatecancerwithsomaticlossofthehomologousrecombinationrepairgenefancaacasereport
_version_ 1724334935793205248