[EFFECT OF NEW ANDROGEN RECEPTOR AXIS-TARGETED AGENTS ON SURVIVAL OF CASTRATION-RESISTANT PROSTATE CANCER].

Q4 Medicine Japanese Journal of Urology Pub Date : 2021-01-01 DOI:10.5980/jpnjurol.112.207
Tomoyuki Shimabukuro, Chietaka Ohmi, Ryoko Nagamitsu, Koji Shiraishi
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Abstract

(Background)The real world's effect of new androgen receptor axis-targeted agents (ARATs) on survival of castration-resistant prostate cancer (CRPC) remains unclear in Japan. (Aims)The primary aim was to determine the clinical benefit of ARATs on survival of CRPC patients. The secondary aim was to evaluate predictive factors affecting the survival of CRPC patients. (Patients and results)Among 236 patients treated with androgen deprivation therapy (ADT), 68 patients developed CRPC; two groups of 34 patients were treated with ARATs (A cases) or conventional ADT (V cases). In a median follow-up of 61.5 months, 20 A and 22 V cases died of cancer. Median survival time (MST) from diagnosis was 99 and 66 months for A and V cases, respectively, and MST from CRPC to death were 50.5 and 44.5 months, respectively. There were no significant differences between both cases. The hazard ratio for death from diagnosis or CRPC progression of the A cases to V cases was 0.711; 95% confidence interval (CI), 0.371 to 1.362; P = 0.3037, or 0.805; 95% CI, 0.434 to 1.491; P=0.4899, respectively. Multivariable analysis revealed that a unique and significant independent prognostic factor from diagnosis was time to CRPC. (Conclusions)In this small retrospective study, we could not determine the clinical benefit of new ARATs compared with conventional ADT on survival of CRPC patients, and a unique and significant independent prognostic factor from diagnosis was time to CRPC. We need to validate these results in a future multi-institutional study.

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[新型雄激素受体轴靶向药物对去势抵抗性前列腺癌存活的影响]。
(背景)在日本,新的雄激素受体轴靶向药物(ARATs)对去势抵抗性前列腺癌(CRPC)存活的影响尚不清楚。(目的)主要目的是确定ARATs对CRPC患者生存的临床获益。次要目的是评估影响CRPC患者生存的预测因素。(患者及结果)236例接受雄激素剥夺治疗(ADT)的患者中,68例发生CRPC;两组34例患者分别接受ARATs (A例)或常规ADT (V例)治疗。在中位61.5个月的随访中,20例a和22例V死于癌症。A型和V型的中位生存期(MST)分别为99和66个月,从CRPC到死亡的中位生存期(MST)分别为50.5和44.5个月。两组间无显著差异。A型病例与V型病例因诊断或CRPC进展死亡的风险比为0.711;95%置信区间(CI) 0.371 ~ 1.362;P = 0.3037,或0.805;95% CI, 0.434 ~ 1.491;分别P = 0.4899。多变量分析显示,从诊断到CRPC的时间是一个独特而重要的独立预后因素。(结论)在这项小型回顾性研究中,我们无法确定新型ARATs与常规ADT相比对CRPC患者生存的临床益处,从诊断到CRPC的时间是一个独特且重要的独立预后因素。我们需要在未来的多机构研究中验证这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Japanese Journal of Urology
Japanese Journal of Urology Medicine-Urology
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