Department of Urology, The University of Tokyo Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 163-0033, Japan.
Division of Innovative Cancer Therapy, Advanced Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Sci Rep. 2023 Feb 15;13(1):2672. doi: 10.1038/s41598-023-29634-5.
The objective of this study was to identify the prognostic factors and to propose a new risk model in metastatic castration-resistant prostate cancer (mCRPC) patients. The clinical data were retrospectively obtained for 102 mCRPC patients who received cancer treatment between 2005 and 2018 at the University of Tokyo Hospital. We investigated clinical and pathological parameters, including prostate-specific antigen (PSA) kinetic profiles under androgen deprivation treatment, and identified predictors of overall survival (OS). The median age and PSA were 73 (Interquartile range [IQR], 68-79) years and 5.00 (IQR, 2.77-13.6) ng/ml. The median follow-up was 34 (IQR, 17-56) months. In univariate analysis, 'lymph node metastasis', 'Hemoglobin (Hb)', 'Time to nadir PSA (TNPSA)', 'PSA doubling time (PSADT)', 'Time to CRPC', and 'presence of pain' were prognostic factors. Multivariate analysis identified 'Hb < 11 g/dL', 'TNPSA < 7 months' and 'PSADT < 5 months' as independent prognostic factors of OS. The high-risk group (patients with two or three factors) demonstrated shorter OS (23 vs. 50 months) with an increased risk of death (HR = 2.997; 95% CI 1.632-5.506; P = 0.0004). The proposed risk stratification model may contribute to the prediction of survival and provide supportive information in treatment decision-making.
本研究旨在确定预后因素,并为转移性去势抵抗性前列腺癌(mCRPC)患者提出新的风险模型。我们回顾性地获取了 2005 年至 2018 年在东京大学医院接受癌症治疗的 102 例 mCRPC 患者的临床数据。我们研究了包括前列腺特异性抗原(PSA)在去势治疗下的动力学特征在内的临床和病理参数,并确定了总生存(OS)的预测因素。中位年龄和 PSA 分别为 73(四分位距 [IQR],68-79)岁和 5.00(IQR,2.77-13.6)ng/ml。中位随访时间为 34(IQR,17-56)个月。单因素分析中,“淋巴结转移”、“血红蛋白(Hb)”、“PSA 达最低点时间(TNPSA)”、“PSA 倍增时间(PSADT)”、“CRPC 发生时间”和“疼痛存在”是预后因素。多因素分析确定“Hb<11 g/dL”、“TNPSA<7 个月”和“PSADT<5 个月”为 OS 的独立预后因素。高风险组(存在两个或三个因素的患者)的 OS 更短(23 个月 vs. 50 个月),死亡风险增加(HR=2.997;95%CI 1.632-5.506;P=0.0004)。该风险分层模型有助于预测生存,并为治疗决策提供支持信息。