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Prostate-specific antigen half-life: a new predictor of progression-free survival and overall survival in Chinese prostate cancer patients

机译:前列腺特异性抗原半衰期:中国前列腺癌​​患者无进展生存和总体生存的新预测因子

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摘要

We investigated the potential value of prostate-specific antigen half-life (PSAHL) and decreasing velocity (PSAVd) to predict progression-free survival (PFS) and overall survival (OS) in Chinese patients with prostate cancer. A total of 153 patients treated with hormonal therapy were included in the study. Of these, 78 patients progressed to hormone-refractory prostate cancer (HRPC) and 24 patients died by the end of follow-up. PSAHL was defined as the time during which prostate-specific antigen (PSA) concentration became half of the initial value during the first hormonal therapy. PSAVd reflected the decreasing velocity of PSA during the first hormonal therapy. PFS was defined as the interval from the beginning of hormonal therapy to HRPC. Cox proportional hazards regression analysis was used to evaluate whether PSAHL and PSAVd were significantly associated with PFS and OS. The median PSAHL and PSAVd were 0.50 months and 33.8 ng mL−1 per month. The median PFS and OS were 22.7 months (95% confidence interval [CI], 22.0–29.6 months) and 43.5 months (95% CI, 37.9–48.4 months), respectively. On univariate and multivariate analysis, long PSAHL (> 0.5 months), metastatic disease, high biopsy Gleason scores (≥ 8) and high nadir PSA (> 0.4 ng mL−1) were all found to be significantly associated with short PFS. Long PSAHL, high nadir PSA and short PSA doubling time (PSADT ≤ 2.0 months) were significantly associated with short OS. There were no significant relationships between PSAVd and either PFS or OS. Thus, PSAHL is a promising new independent predictor of survival. Patients with long PSAHL were identified as those at high risk for a relatively short PFS and OS.
机译:我们调查了前列腺特异性抗原半衰期(PSAHL)和降低速度(PSAVd)的潜在价值,以预测中国前列腺癌​​患者的无进展生存期(PFS)和总体生存期(OS)。本研究共纳入153名接受激素治疗的患者。其中,有78例患者发展为激素难治性前列腺癌(HRPC),有24例患者在随访结束时死亡。 PSAHL定义为在第一次激素治疗期间前列腺特异性抗原(PSA)浓度变为初始值一半的时间。 PSAVd反映了首次激素治疗期间PSA的速度下降。 PFS被定义为从激素治疗开始到HRPC的时间间隔。使用Cox比例风险回归分析来评估PSAHL和PSAVd是否与PFS和OS显着相关。 PSAHL和PSAVd的中位数为0.50个月,每月33.8 ng mL -1 。 PFS和OS的中位数分别为22.7个月(95%置信区间[CI],22.0-29.6个月)和43.5个月(95%CI,37.9-48.4个月)。单因素和多因素分析显示,长期PSAHL(> 0.5个月),转移性疾病,高活检格里森评分(≥8)和高最低点PSA(> 0.4 ng mL -1 )均显着与短PFS相关。较长的PSAHL,较高的最低点PSA和较短的PSA加倍时间(PSADT≤2.0个月)与较短的OS显着相关。 PSAVd与PFS或OS之间没有显着关系。因此,PSAHL是有希望的新的生存独立预测因子。 PSAHL较长的患者被确定为PFS和OS相对较短的高风险患者。

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