A Case Report of Metastatic Castration-Resistant Prostate Cancer Harboring a PTEN Loss

被引:3
作者
Myint, Zin W. [1 ,2 ]
Allison, Derek B. [2 ,3 ,4 ]
Ellis, Carleton S. [2 ,5 ]
机构
[1] Univ Kentucky, Div Med Oncol, Dept Internal Med, Lexington, KY 40506 USA
[2] Univ Kentucky, Markey Canc Ctr, Lexington, KY 40506 USA
[3] Univ Kentucky, Dept Urol, Lexington, KY USA
[4] Univ Kentucky, Dept Pathol & Lab Med, Lexington, KY USA
[5] Univ Kentucky, Dept Pharm, Lexington, KY USA
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
关键词
metastatic castration refractory prostate cancer; PI3K; AKT pathway; carboplatin; abiraterone acetate; ATM; Chk2; p53 signal pathway; TUMOR-SUPPRESSOR; INCREASED SURVIVAL; RADIATION-THERAPY; PLUS PREDNISONE; DNA-REPAIR; OPEN-LABEL; ABIRATERONE; MEN; MITOXANTRONE; CABAZITAXEL;
D O I
10.3389/fonc.2021.731002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment landscape of metastatic castration-resistant prostate cancer (mCRPC) has dramatically improved over the last decade; however, patients with visceral metastases are still faced with poor outcomes. Phosphatase and tensin homolog (PTEN) loss is observed in 40%-60% of mCRPC patients and is also associated with a poor prognosis. Several PI3K/AKT/mTOR pathway inhibitors have been studied, with disappointing anti-tumor activity. Here, we present a case of a patient with heavily treated mCRPC who had a modest tumor response to concurrent carboplatin, abiraterone acetate/prednisone, and liver-directed radiation therapy. We discuss the potential rationale supporting the use of this combination therapy and its safety in mCRPC. While the underlying basic mechanism of our patient's anti-tumor response remains uncertain, we suggest that further prospective studies are warranted to evaluate whether this combination therapy is effective in this population of patients with pre-treated mCRPC and PTEN loss.
引用
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页数:7
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