Gleason Pattern 5 May Be a Prognostic Factor in Radium-223 Treatment.

Cancer diagnosis & prognosis Pub Date : 2024-07-03 eCollection Date: 2024-07-01 DOI:10.21873/cdp.10345
Mitsuhisa Nishimoto, Kazutoshi Fujita, Aritoshi Ri, Saizo Fujimoto, Yasuo Oguma, Shingo Toyoda, Mamoru Hashimoto, Takashi Kikuchi, Shogo Adomi, Yoshitaka Saito, Yasunori Mori, Takafumi Minami, Masahiro Nozawa, Kazuhiro Yoshimura, Makoto Hosono, Hirotsugu Uemura
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Abstract

Background/aim: Radium-223 treatment reduces the risk of death in patients with metastatic castration-resistant prostate cancer (CRPC). This study analyzed the prognostic factors in patients treated with radium-223 dichloride.

Patients and methods: Patients who received radium-223 dichloride were retrospectively analyzed. Prostate-specific antigen (PSA) response and alkaline phosphatase (ALP) decline rates were analyzed. Overall survival (OS) was evaluated using Kaplan-Meier curves, and prognostic factors for OS were assessed using Cox proportional hazards analysis.

Results: Fifty-six patients were included in the study. The five-year OS rate in patients after diagnosis of CRPC was 62.2% [95% confidence interval (CI)=27.55-112.45], while the five-year OS rate in patients at the initiation of radium-223 treatment was 21.3% (95%CI=17.20-36.79). Six patients (11.1%) had a >50% PSA decline rate, and 10 (17.9%) had a >50% ALP decline rate. Cox proportional hazards analysis showed that PSA levels at the initiation of radium-223 treatment [hazard ratio (HR)=1.00; 95%CI=1.00-1.00; p=0.0054] and Gleason Pattern (GP) 5 (HR=5.42; 95%CI=1.08-27.27; p=0.0400) were associated with OS. Patients with GP 5 had a significantly poorer prognosis compared with patients with a GP ≤4. Early administration of radium-223 as a first- or second-line treatment was not associated with OS compared with late administration of radium-223 as a third-line or later treatment.

Conclusion: GP 5 and high PSA levels at radium-223 initiation were associated with worse OS. Radium-223 as first- or second-line treatment was not associated with OS. Therefore, a treatment strategy for CRPC based on GP 5 is needed.

Gleason模式5可能是镭-223治疗的预后因素。
背景/目的:镭-223治疗可降低转移性去势抵抗性前列腺癌(CRPC)患者的死亡风险。本研究分析了接受二氯化镭-223治疗的患者的预后因素:对接受二氯化镭-223治疗的患者进行回顾性分析。分析了前列腺特异性抗原(PSA)反应和碱性磷酸酶(ALP)下降率。采用Kaplan-Meier曲线评估总生存期(OS),采用Cox比例危险分析评估OS的预后因素:研究共纳入56名患者。确诊CRPC后患者的五年OS率为62.2%[95%置信区间(CI)=27.55-112.45],而开始接受镭-223治疗时患者的五年OS率为21.3%(95%CI=17.20-36.79)。6名患者(11.1%)的PSA下降率大于50%,10名患者(17.9%)的ALP下降率大于50%。Cox比例危险分析显示,开始接受镭-223治疗时的PSA水平[危险比(HR)=1.00;95%CI=1.00-1.00;P=0.0054]和Gleason模式(GP)5(HR=5.42;95%CI=1.08-27.27;P=0.0400)与OS相关。与GP≤4的患者相比,GP 5的患者预后明显较差。与作为三线或更晚治疗的晚期镭-223相比,作为一线或二线治疗的早期镭-223与OS无关:结论:开始使用镭-223时的GP 5和高PSA水平与较差的OS有关。镭-223作为一线或二线治疗与OS无关。因此,需要根据GP 5制定CRPC治疗策略。
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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