Wang Yu-Jen, Tseng Chi-Shin, Huang Chao-Yuan, Chen Chung-Hsin, Wang So-Meng, Huang Kuo-How, Chow Po-Ming, Pu Yeong-Shiau, Chueh Jeff Shih-Chieh, Chung Shiu-Dong, Cheng Jason Chia-Hsien
Department of Radiation Oncology, Fu Jen Catholic University Hospital, New Taipei City 24352, Taiwan.
School of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei City 242062, Taiwan.
Biomedicines. 2024 Oct 8;12(10):2275. doi: 10.3390/biomedicines12102275.
Patients with non-metastatic castration-resistant prostate cancer (nmCRPC) and high-risk features frequently have progression to life-threatening metastasis without second-generation antiandrogens. This study investigated nmCRPC patients for the survival and prognostic factors from a cohort before the approved use of second-generation antiandrogens. From March 2016 to January 2021, 326 patients treated with second-generation antiandrogens for metastatic castration-resistant prostate cancer (mCRPC) or metastatic castration-sensitive prostate cancer were retrieved. Forty-four patients experiencing nmCRPC with no use of second-generation antiandrogens were reviewed. The prognostic factors, at initial diagnosis or at nmCRPC, associated with metastasis-free survival (MFS) and overall survival (OS) were analyzed. The median follow-up time after nmCRPC was 46 months. The median PSA level at nmCRPC was 2.7 ng/mL. Thirty-eight of forty-four patients with nmCRPC had a PSA doubling time (PSADT) of 10 months or shorter, and the median PSADT was 4 months. The median OS from nmCRPC was 53 months, and the median interval for nmCRPC patients progressing to mCRPC was 20 months. Upon univariate analysis, PSADT < 10 months ( = 0.049) and the very-high-risk group at the initial diagnosis ( = 0.043) were associated with significantly shorter post-nmCRPC MFS. The very-high-risk group ( = 0.031) was associated with significantly worse post-nmCRPC OS. In terms of survivals from the initial diagnosis of prostate cancer, Gleason grade ≥ 8 was the only independent factor with MFS and OS. Without second-generation antiandrogens, nmCRPC patients with PSADT <10 months and in the initial very-high-risk group developed subsequent mCRPC in a significantly faster fashion. Patients of the very-high-risk group had shorter survival rates after nmCRPC.
非转移性去势抵抗性前列腺癌(nmCRPC)且具有高危特征的患者,如果不使用第二代抗雄激素药物,往往会进展为危及生命的转移。本研究在第二代抗雄激素药物获批使用之前,对一组nmCRPC患者的生存情况和预后因素进行了调查。2016年3月至2021年1月,共检索到326例接受第二代抗雄激素药物治疗的转移性去势抵抗性前列腺癌(mCRPC)或转移性去势敏感性前列腺癌患者。对44例未使用第二代抗雄激素药物的nmCRPC患者进行了回顾性分析。分析了在初始诊断或nmCRPC时与无转移生存期(MFS)和总生存期(OS)相关的预后因素。nmCRPC后的中位随访时间为46个月。nmCRPC时的中位PSA水平为2.7 ng/mL。44例nmCRPC患者中有38例的PSA倍增时间(PSADT)为10个月或更短,中位PSADT为4个月。nmCRPC后的中位OS为53个月,nmCRPC患者进展为mCRPC的中位间隔时间为20个月。单因素分析显示,PSADT<10个月(P = 0.049)和初始诊断时的极高危组(P = 0.043)与nmCRPC后的MFS显著缩短相关。极高危组(P = 0.031)与nmCRPC后的OS显著较差相关。就前列腺癌初始诊断后的生存期而言,Gleason分级≥8是MFS和OS的唯一独立因素。在没有第二代抗雄激素药物的情况下,PSADT<10个月且处于初始极高危组的nmCRPC患者发展为后续mCRPC的速度明显更快。极高危组患者nmCRPC后的生存率较低。