Nishimoto Mitsuhisa, De Velasco Marco A, Yamamoto Yutaka, Fujimoto Saizo, Akashi Yasunori, Toyoda Shingo, Hashimoto Mamoru, Adomi Shogo, Banno Eri, Saito Yoshitaka, Minami Takafumi, Hirayama Akihide, Yoshimura Kazuhiro, Uemura Hirotsugu, Fujita Kazutoshi
Department of Urology, Kindai University Faculty of Medicine, Osakasayama, Japan.
Department of Genome Biology, Kindai University Faculty of Medicine, Osakasayama, Japan.
Prostate. 2025 May;85(7):631-637. doi: 10.1002/pros.24865. Epub 2025 Jan 31.
The efficacy of abiraterone acetate varies among patients with high-risk metastatic castration-sensitive prostate cancer (mCSPC). Both androgen receptor (AR) and cytokeratin 18 (CK18) are markers of the luminal lineage of prostate cancer, and their expression levels have been suggested to affect the response to androgen deprivation therapy (ADT). This study aimed to predict the efficacy of abiraterone acetate in high-risk mCSPC via immunohistochemical staining of biopsy specimens obtained at the time of prostate cancer diagnosis.
We retrospectively analyzed 44 patients treated with abiraterone acetate in combination with ADT. AR and CK18 expression in prostate biopsy specimens were assessed using immunohistochemical staining.
AR and CK18 staining was not significantly associated with overall survival (OS). However, low AR staining was significantly associated with a shorter time to castration-resistant prostate cancer (TTCRPC) compared with high AR staining (log-rank test, p = 0.018). Similarly, low CK18 staining was significantly associated with a shorter TTCRPC compared with high CK18 staining (log-rank test, p = 0.037).
Immunohistochemical analysis of AR or CK18 expression in biopsy specimens may serve as a predictive biomarker of high-risk mCSPC treated with abiraterone acetate.
None.
醋酸阿比特龙在高危转移性去势敏感性前列腺癌(mCSPC)患者中的疗效存在差异。雄激素受体(AR)和细胞角蛋白18(CK18)均为前列腺癌管腔谱系的标志物,且有研究表明它们的表达水平会影响对雄激素剥夺治疗(ADT)的反应。本研究旨在通过对前列腺癌诊断时获取的活检标本进行免疫组织化学染色,预测醋酸阿比特龙在高危mCSPC中的疗效。
我们回顾性分析了44例接受醋酸阿比特龙联合ADT治疗的患者。采用免疫组织化学染色评估前列腺活检标本中AR和CK18的表达。
AR和CK18染色与总生存期(OS)无显著相关性。然而,与高AR染色相比,低AR染色与去势抵抗性前列腺癌发生时间(TTCRPC)较短显著相关(对数秩检验,p = 0.018)。同样,与高CK18染色相比,低CK18染色与较短的TTCRPC显著相关(对数秩检验,p = 0.037)。
对活检标本中AR或CK18表达进行免疫组织化学分析,可能作为醋酸阿比特龙治疗高危mCSPC的预测生物标志物。
无。