TY - JOUR
T1 - Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA
T2 - A case report
AU - Hongo, Hiroshi
AU - Kosaka, Takeo
AU - Aimono, Eriko
AU - Nishihara, Hiroshi
AU - Oya, Mototsugu
N1 - Funding Information:
This study was supported in part by Grants-in-Aid for Scientific Research (#17 K11158 to T. Kosaka) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan and by a research grant to T. Kosaka from the Takeda Science Foundation, Japan.
Publisher Copyright:
© 2020 The Author(s).
PY - 2020/1/13
Y1 - 2020/1/13
N2 - 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.
AB - 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.
KW - Castration-resistant prostate cancer
KW - FANCA
KW - Genomic analysis
KW - Homologous recombination repair
KW - Next-generation sequencing
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U2 - 10.1186/s13000-019-0916-z
DO - 10.1186/s13000-019-0916-z
M3 - Article
C2 - 31931827
AN - SCOPUS:85077785834
SN - 1746-1596
VL - 15
JO - Diagnostic Pathology
JF - Diagnostic Pathology
IS - 1
M1 - 5
ER -