Nagaya Naoya, Kanayama Mayuko, Nagata Masayoshi, Horie Shigeo
Department of Urology, Juntendo University Graduate School of Medicine, Bunkyo, Japan.
Front Oncol. 2020 Apr 8;10:495. doi: 10.3389/fonc.2020.00495. eCollection 2020.
Serial analysis of circulating tumor cells (CTCs) such as androgen receptor splice variant 7 is useful in selecting treatments for castration-resistant prostate cancer (CRPC). We report a case who had been positive for androgen receptor splice variant 7 in CTCs before docetaxel, and was subsequently treated with abiraterone rechallenge because of the negative conversion of androgen receptor splice variant 7 following docetaxel. Although, the rechallenge of anti-androgen agent based on CTCs analysis is expected to be an effective approach, it is yet to be reported. Thus, we chose the candidate for abiraterone rechallenge based on serial CTCs analyses by the AdnaTest. As a result, the patient responded to abiraterone that he once had developed resistance to. Our findings reinforce the utility of AR-V7 as a biomarker in the setting of post-chemo androgen-targeted-therapy rechallenge.
对循环肿瘤细胞(CTC)进行系列分析,如分析雄激素受体剪接变体7,有助于为去势抵抗性前列腺癌(CRPC)选择治疗方案。我们报告了1例病例,该患者在多西他赛治疗前其CTC中的雄激素受体剪接变体7呈阳性,多西他赛后由于雄激素受体剪接变体7转阴,随后接受阿比特龙再激发治疗。虽然基于CTC分析进行抗雄激素药物再激发治疗有望成为一种有效的方法,但尚未见相关报道。因此,我们通过AdnaTest对CTC进行系列分析来选择阿比特龙再激发治疗的候选患者。结果,该患者对他曾产生过耐药性的阿比特龙产生了反应。我们的研究结果强化了AR-V7作为化疗后雄激素靶向治疗再激发背景下生物标志物的效用。