Department of Urology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Strategic Investigation on Comprehensive Cancer Network, Interfaculty Initiative in Information Studies/Graduate School of Interdisciplinary Information Studies, the University of Tokyo, Tokyo, Japan.
PLoS One. 2020 Jan 27;15(1):e0226219. doi: 10.1371/journal.pone.0226219. eCollection 2020.
The aim of this study is to elucidate the clinical significance of prostate-specific membrane antigen (PSMA) expression in circulating tumor cells (CTCs) from castration-resistant prostate cancer (CRPC) patients. We analyzed a total of 203 CTC samples from 79 CRPC patients to investigate the proportion of positive mRNA expressions at different treatment phases. Among them, we elected to focus on specimens from 56 CRPC patients who progressed on therapy and were subsequently provided a new treatment (treatment-switch cohort). In this cohort, we investigated the association between PSMA expression in CTCs and treatment response. CTCs were detected in 55/79 patients and median serum PSA in CTC-positive patients was 67.0 ng/ml. In the treatment-switch cohort of 56 patients, 20 patients were positive for PSMA in CTCs. PSMA expression was inversely associated with percentage of change in prostate-specific antigen (PSA). The median PSA progression-free survival and overall survival were significantly shorter in the PSMA-positive cohort. Furthermore, PSMA expression was predictive of poorer treatment response, shorter PSA progression-free survival and overall survival. PSMA expression in circulating tumor cells may be a novel poor prognostic marker for CRPC.
本研究旨在阐明去势抵抗性前列腺癌(CRPC)患者循环肿瘤细胞(CTC)中前列腺特异性膜抗原(PSMA)表达的临床意义。我们分析了 79 例 CRPC 患者的 203 个 CTC 样本,以研究不同治疗阶段阳性 mRNA 表达的比例。其中,我们选择关注 56 例治疗进展后接受新治疗(治疗转换队列)的 CRPC 患者的标本。在该队列中,我们研究了 CTC 中 PSMA 表达与治疗反应之间的关系。在 79 例患者中有 55 例检测到了 CTC,CTC 阳性患者的中位血清 PSA 为 67.0ng/ml。在 56 例治疗转换队列的患者中,有 20 例 CTC 中 PSMA 呈阳性。PSMA 表达与前列腺特异性抗原(PSA)变化百分比呈负相关。PSMA 阳性组的 PSA 无进展生存期和总生存期明显缩短。此外,PSMA 表达可预测治疗反应较差、PSA 无进展生存期和总生存期较短。循环肿瘤细胞中 PSMA 的表达可能是 CRPC 的一种新的预后不良标志物。