A Prospective Randomised Trial to Determine the Effect of a Reduced Versus Standard Dose of Enzalutamide on Side Effects in Frail Patients with Prostate Cancer.

IF 8.3 1区 医学 Q1 ONCOLOGY European urology oncology Pub Date : 2024-12-01 Epub Date: 2024-03-13 DOI:10.1016/j.euo.2024.02.009
Emmy Boerrigter, Joanneke K Overbeek, Guillemette E Benoist, Diederik M Somford, Paul Hamberg, Jolien Tol, Brian Scholtes, Annelieke E C A B Willemsen, Laurien M Buffart, Roy P C Kessels, Niven Mehra, Inge M van Oort, Nielka P van Erp
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Abstract

Background and objective: Enzalutamide is a potent androgen receptor signalling inhibitor, effectively used for the treatment of different stages of prostate cancer. Side effects occur frequently at the registered dose, whilst a lower dose might be equally effective. Therefore, the aim of this study is to determine the effect of a reduced dose of enzalutamide on side effects in frail patients with prostate cancer.

Methods: This multicentre randomised trial compared the standard enzalutamide dose of 160 mg once daily (OD) with a reduced dose of 120 mg OD in frail patients with prostate cancer. Fatigue, cognitive side effects, and depressive symptoms were measured by the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) questionnaire, Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) questionnaire, and Geriatric Depression Scale-15 (GDS-15). Linear mixed-effect models were used to study differences in side effects over time between both groups.

Key findings and limitations: In total, 52 patients were included in the analysis (25 reduced dose and 27 standard dose). Patients treated with the reduced dose had significantly lower fatigue after 24 wk than those with the standard dose (difference FACIT-Fatigue 6.2; 95% confidence interval 1.4-11.0; p = 0.01). Patients treated with the reduced dose showed stable fatigue, cognitive side effects, and depressive symptoms over time, whilst patients with the standard dose showed significantly worse side effects after 24 wk than at baseline.

Conclusions and clinical implications: A reduced dose of enzalutamide results in less fatigue, cognitive side effects, and depressive symptoms in frail patients with prostate cancer than the standard dose, without any indication of interference with efficacy endpoints.

Patient summary: In this report, we looked at the side effects of enzalutamide at two dose levels. We found that, in frail patients, three tablets a day result in less fatigue than four tablets a day. Patients treated with four tablets a day showed an increase in fatigue, cognitive side effects, and depression. We conclude that a lower dose of three tablets can be used to alleviate side effects without indications for less efficacy.

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前瞻性随机试验:确定恩杂鲁胺的减量剂量与标准剂量对体弱前列腺癌患者副作用的影响
背景和目的:恩杂鲁胺是一种强效的雄激素受体信号抑制剂,可有效治疗不同阶段的前列腺癌。注册剂量经常出现副作用,而较低剂量可能同样有效。因此,本研究旨在确定减少恩杂鲁胺剂量对体弱前列腺癌患者副作用的影响:这项多中心随机试验比较了前列腺癌体弱患者每日一次160毫克的恩杂鲁胺标准剂量和120毫克的减量剂量。疲劳、认知副作用和抑郁症状通过慢性疾病治疗功能评估-疲劳(FACIT-Fatigue)问卷、癌症治疗功能评估-认知功能(FACT-Cog)问卷和老年抑郁量表-15(GDS-15)进行测量。采用线性混合效应模型研究两组患者随时间变化的副作用差异:共有52名患者参与了分析(25名减量患者和27名标准剂量患者)。接受减量治疗的患者在24周后的疲劳感明显低于接受标准剂量治疗的患者(FACIT-疲劳感差异为6.2;95%置信区间为1.4-11.0;P = 0.01)。随着时间的推移,接受减量治疗的患者显示出稳定的疲劳、认知副作用和抑郁症状,而接受标准剂量治疗的患者在24周后的副作用明显比基线时严重:与标准剂量相比,减量恩杂鲁胺可减少体弱前列腺癌患者的疲劳、认知副作用和抑郁症状,且没有任何迹象表明会干扰疗效终点。患者总结:在这份报告中,我们研究了两种剂量水平的恩杂鲁胺的副作用。我们发现,对于身体虚弱的患者来说,每天服用三片比每天服用四片更容易产生疲劳感。而每天服用四片的患者,疲劳、认知副作用和抑郁的程度都有所增加。我们的结论是,使用较低剂量的三片药片可减轻副作用,但没有降低疗效的迹象。
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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
期刊最新文献
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