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镭-223治疗转移性去势抵抗性前列腺癌患者:临床实践中的疗效与安全性

Radium-223 in patients with metastatic castration-resistant prostate cancer: Efficacy and safety in clinical practice.

作者信息

Prelaj Arsela, Rebuzzi Sara Elena, Buzzacchino Federica, Pozzi Chiara, Ferrara Carla, Frantellizzi Viviana, Follacchio Giulia Anna, Civitelli Liana, De Vincentis Giuseppe, Tomao Silverio, Bianco Vincenzo

机构信息

Department of Radiological, Oncological and Anatomo-Pathological Sciences, 'Sapienza' University of Rome, Policlinico Umberto I, I-00161 Rome, Italy.

Department of Medical Oncology, IRCCS San Martino IST, I-16132 Genoa, Italy.

出版信息

Oncol Lett. 2019 Feb;17(2):1467-1476. doi: 10.3892/ol.2018.9785. Epub 2018 Nov 30.

Abstract

Radium-223 has improved overall survival (OS) and reduced symptomatic skeletal events (SSE) in patients with metastatic castration-resistant prostate cancer (mCRPC) and bone metastases (ALSYMPCA trial). Our aim was to assess clinical and biochemical factors related to survival, safety and survival outcomes of Radium-223 in a clinical practice setting. We retrospectively analysed 32 mCRPC patients treated with Radium-223, assessing bone scan, pain reduction, alkaline phosphatase (ALP) and prostate-specific antigen (PSA) response (≥30% reduction). At scintigraphic assessment, 41% had partial response with a disease control rate of 91%; 56% had ALP response and 25% had PSA response; 41% had pain reduction with pain control of 72%. Scintigraphic response and stability were correlated with longer median progression-free survival (mPFS) (13 and 12 vs. 6 months; P=0.002) and mOS (16 and 12 vs. 6 months; P=0.003). ALP response was associated with longer mPFS (13 vs. 12 months; P=0.2) and mOS (16 vs. 12 months; P=0.2). PSA response was associated with longer mPFS (13 vs. 12 months; P=0.02), whereas mOS could not be computed. Pain response and stability were associated with survival benefit according to mPFS (13 and 12 vs. 9 months) and mOS (both 16 vs. 12 months) without statistical significance. Baseline ALP <220 UI/l, Eastern Cooperative Oncology Group (ECOG) performance status 0 and absence of previous chemotherapy correlated with statistically significantly longer survival outcomes. Skeletal-related events (SRE) occurred in three patients and median time to first SRE was 9.5 months, mPFS was 12 months and mOS 14 months. G3-G4 toxicities developed in 16% of patients. Our results are in line with those reported in the pivotal trial and in other retrospective studies. In conclusion, Radium-223 was associated with high scintigraphic, biochemical and pain response rates and was tolerated well by most patients. Response to Radium-223 and better baseline factors correlated to longer survival in clinical practice experience as in the clinical trial setting.

摘要

镭-223已改善转移性去势抵抗性前列腺癌(mCRPC)和骨转移患者的总生存期(OS)并减少了有症状的骨相关事件(SSE)(ALSYMPCA试验)。我们的目的是在临床实践环境中评估与镭-223的生存、安全性和生存结果相关的临床和生化因素。我们回顾性分析了32例接受镭-223治疗的mCRPC患者,评估骨扫描、疼痛减轻情况、碱性磷酸酶(ALP)和前列腺特异性抗原(PSA)反应(降低≥30%)。在闪烁扫描评估中,41%有部分反应,疾病控制率为91%;56%有ALP反应,25%有PSA反应;41%疼痛减轻,疼痛控制率为72%。闪烁扫描反应和稳定性与更长的中位无进展生存期(mPFS)(分别为13个月和12个月对6个月;P = 0.002)和mOS(分别为16个月和12个月对6个月;P = 0.003)相关。ALP反应与更长的mPFS(13个月对12个月;P = 0.2)和mOS(16个月对12个月;P = 0.2)相关。PSA反应与更长的mPFS(13个月对12个月;P = 0.02)相关,而mOS无法计算。根据mPFS(分别为13个月和12个月对9个月)和mOS(均为16个月对12个月),疼痛反应和稳定性与生存获益相关,但无统计学意义。基线ALP<220 UI/l、东部肿瘤协作组(ECOG)体能状态为0以及未接受过先前化疗与统计学上显著更长的生存结果相关。三名患者发生了骨相关事件(SRE),首次SRE的中位时间为9.5个月,mPFS为12个月,mOS为14个月。16%的患者出现3-4级毒性反应。我们的结果与关键试验和其他回顾性研究中报告的结果一致。总之,镭-223具有较高的闪烁扫描、生化和疼痛反应率,并且大多数患者耐受性良好。在临床实践经验中,对镭-223的反应以及更好的基线因素与更长的生存期相关,如同在临床试验环境中一样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51bf/6341517/3ac22723c926/ol-17-02-1467-g00.jpg

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