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探究支持初发性临床淋巴结阳性激素敏感性前列腺癌治疗方案的III期试验的最新证据。

Investigating the Latest Evidence from Phase III Trials Supporting Treatment Options for De novo Clinically Lymph Node-Positive Hormone-Sensitive Prostate Cancer.

作者信息

Elewaily Mohamed Ibrahim, Maniam Akash, Tree Alison, Banna Giuseppe Luigi

机构信息

University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Department of Oncology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK.

出版信息

Curr Oncol Rep. 2025 May;27(5):572-583. doi: 10.1007/s11912-025-01665-3. Epub 2025 Apr 1.

Abstract

PURPOSE OF REVIEW

The introduction of PSMA-PET/CT scans is expected to increase the incidence of clinically lymph node-positive metastatic hormone-sensitive prostate cancer (mHSPC). The 8th AJCC-TNM classify disease with metastasis limited to pelvic nodes (cN1M0) and nonregional lymph nodes (M1a) as stage IV. To date, there is limited prospective evidence for management of this subgroup. Additionally, no specific recommendations currently exist for managing M1a as a distinct condition but as a part of CHAARTED low volume disease (LVD). Our review examines relevant results from phase III trials examining the management of clinically positive nodal disease over the last decade.

RECENT FINDINGS

STAMPEDE is the only phase III trial that gave recent data about cN1M0 and isolated M1a management. Cohort sub-analysis of the control arm showed improved failure-free survival after local radiotherapy (RT) plus Androgen Deprivation Therapy (ADT), while metastasis-free survival benefit from Abiraterone Acetate with Prednisolone (AAP) addition was noted when compared to standard of care (SOC), awaiting the overall survival (OS) benefit result. The STAMPEDE H arm showed a marginal significance of M1a stratified OS after RT. Future trials, including PEARLS, ALADDIN and STAMPEDE2, are expected to offer more insights. Interventional Phase III trials directed to clinically node positive patients are still needed to aid deciding on the best management, and nodal metastasis number and size impact on prognosis.

摘要

综述目的

前列腺特异性膜抗原正电子发射断层扫描/计算机断层扫描(PSMA-PET/CT)的引入预计会增加临床淋巴结阳性转移性激素敏感性前列腺癌(mHSPC)的发病率。美国癌症联合委员会(AJCC)第8版肿瘤分期手册将转移局限于盆腔淋巴结(cN1M0)和非区域淋巴结(M1a)的疾病归类为IV期。迄今为止,针对该亚组治疗的前瞻性证据有限。此外,目前尚无针对将M1a作为一种独特情况进行管理的具体建议,而是将其作为CHAARTED低负荷疾病(LVD)的一部分。我们的综述考察了过去十年中关于临床淋巴结阳性疾病管理的III期试验的相关结果。

最新发现

STAMPEDE是唯一一项给出了关于cN1M0和孤立M1a管理的近期数据的III期试验。对照组的队列亚组分析显示,局部放疗(RT)联合雄激素剥夺治疗(ADT)后无失败生存期有所改善,而与标准治疗(SOC)相比,添加醋酸阿比特龙与泼尼松龙(AAP)可使无转移生存期受益,目前正在等待总生存期(OS)受益结果。STAMPEDE H组显示RT后M1a分层的OS有边缘显著性差异。未来的试验,包括PEARLS试验、ALADDIN试验和STAMPEDE2试验,预计将提供更多见解。仍需要针对临床淋巴结阳性患者的干预性III期试验,以帮助确定最佳治疗方案,以及淋巴结转移数量和大小对预后的影响。

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