Department of Urology UROSUD, La Croix du Sud Hospital, Toulouse, France; Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza and University of Turin, Turin, Italy.
Biostatistics & Health Data Science Unit, Institut Claudius Regaud, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Eur Urol Oncol. 2024 Jun;7(3):494-500. doi: 10.1016/j.euo.2023.09.020. Epub 2023 Oct 6.
High-risk prostate cancer (PCa) patients frequently experience recurrence and progression after radical prostatectomy (RP). Neoadjuvant androgen deprivation therapy (ADT) has not demonstrated a clear oncological benefit and is not currently recommended.
The SUGAR trial is the first phase 2, randomised, controlled, multicentre, noncommercial, open-label study investigating single-agent perioperative darolutamide compared with the standard of care (ie, upfront RP, without neoadjuvant ADT).
DESIGN, SETTING, AND PARTICIPANTS: SUGAR aims to randomise 240 men affected by nonmetastatic PCa, with the major eligibility criteria being International Society of Urological Pathology grade group ≥4, seminal vesicle invasion at magnetic resonance imaging and/or clinically node-positive disease. Patients in the experimental arm will undergo neoadjuvant darolutamide monotherapy, RP, and adjuvant darolutamide, completing 9 mo of treatment.
The primary endpoint is noncurable recurrence-free survival, an innovative and clinically meaningful measure; the secondary endpoints encompass safety; recurrence-free, metastasis-free, and overall survival; pathological response; and quality of life. A predictive biomarker analysis will also be performed.
Initial data suggest that intensified neoadjuvant treatment with androgen receptor signalling inhibitors (ARSIs) is associated with a sustained pathological response and may improve outcomes, via tumour downstaging and micrometastasis eradication. ARSI monotherapy could further enhance tolerability.
SUGAR will provide efficacy and safety information on perioperative darolutamide monotherapy compared with upfront RP, in a contemporary high-risk PCa population undergoing surgery.
The on-going SUGAR clinical trial evaluates 9 mo of darolutamide treatment in addition to radical prostatectomy, in men affected by prostate cancer with specific high-risk characteristics. It investigates whether this hormonal treatment can lower the rates of noncurable recurrences, maintaining a favourable tolerability profile.
高危前列腺癌(PCa)患者在根治性前列腺切除术(RP)后经常复发和进展。新辅助雄激素剥夺疗法(ADT)并未显示出明确的肿瘤学益处,目前不推荐使用。
SUGAR 试验是第一项 II 期、随机、对照、多中心、非商业性、开放标签研究,旨在研究单药围手术期达罗他胺与标准治疗(即,不进行新辅助 ADT 的 upfront RP)相比的疗效。
设计、设置和参与者:SUGAR 旨在随机分配 240 名患有非转移性 PCa 的男性患者,主要入选标准为国际泌尿病理学会(ISUP)分级组≥4 级、磁共振成像(MRI)显示精囊受侵和/或临床淋巴结阳性疾病。实验组患者将接受新辅助达罗他胺单药治疗、RP 和辅助达罗他胺治疗,完成 9 个月的治疗。
主要终点是不可治愈的无复发生存率,这是一项创新且具有临床意义的指标;次要终点包括安全性、无复发生存率、无转移生存率和总生存率、病理反应以及生活质量。还将进行预测生物标志物分析。
初步数据表明,强化新辅助治疗使用雄激素受体信号抑制剂(ARSIs)与持续的病理反应相关,并可能通过肿瘤降期和微转移消除来改善结局。ARSI 单药治疗可能进一步提高耐受性。
SUGAR 将提供围手术期达罗他胺单药治疗与 upfront RP 相比的疗效和安全性信息,适用于接受手术的当代高危 PCa 人群。
正在进行的 SUGAR 临床试验评估了 9 个月的达罗他胺治疗,作为高危前列腺癌男性患者根治性前列腺切除术的辅助治疗。它调查了这种激素治疗是否可以降低不可治愈的复发率,同时保持良好的耐受性。