Berruti Alfredo, Bracarda Sergio, Caffo Orazio, Cortesi Enrico, D'Angelillo Rolando, Del Re Marzia, Facchini Gaetano, Pappagallo Giovanni, Procopio Giuseppe, Sabbatini Roberto, Santini Daniele
Unit of Medical Oncology, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Italy.
Medical and Translational Oncology Unit, Department of Oncology, Azienda Ospedaliera Santa Maria, Terni, Italy.
Cancer Treat Rev. 2023 Apr;115:102525. doi: 10.1016/j.ctrv.2023.102525. Epub 2023 Feb 14.
Non-metastatic castration resistant prostate cancer (nmCRPC) is a clinical setting defined as confirmed rising levels of PSA in patients treated with ADT but without detectable metastases on conventional imaging with computerized tomography (CT) and technetium-99 m scintigraphy. Men with nmCRPC and a PSA doubling time (PSADT) ≤ 10 months are considered at high risk of rapidly developing metastases with a consequent possible impact on survival. Three recent phase III trials have demonstrated, in this setting, the efficacy of adding a next-generation androgen receptor targeted agent (ARTA) to ADT in respect to ADT only, in delaying the development of metastases (metastasis-free survival, MFS) and prolong overall survival. The magnitude of clinical benefit of these agents was even more meaningful if considering the low incidence of drug related adverse events. Our review described the latest advances in the management of nmCRPC, deriving from the pivotal clinical trials, SPARTAN, PROSPER and ARAMIS, in order to support clinicians to optimally manage these patients. Of note, the emergence of novel, more accurate, next-generation imaging techniques (including Ga PSMA-PET/CT), as well as eventual future tumor biomarkers, is modifying the entity and definition of the nmCRPC setting, with a consequent impact on patient's diagnosis and management.
非转移性去势抵抗性前列腺癌(nmCRPC)是一种临床情况,定义为接受雄激素剥夺治疗(ADT)的患者前列腺特异性抗原(PSA)水平持续升高,但在计算机断层扫描(CT)和锝-99m闪烁扫描等传统影像学检查中未发现转移。nmCRPC且前列腺特异性抗原倍增时间(PSADT)≤10个月的男性被认为有快速发生转移的高风险,进而可能影响生存。最近的三项III期试验表明,在这种情况下,相较于单纯ADT,在ADT基础上加用新一代雄激素受体靶向药物(ARTA)可延缓转移的发生(无转移生存期,MFS)并延长总生存期。如果考虑到药物相关不良事件的低发生率,这些药物的临床获益程度更具意义。我们的综述描述了nmCRPC管理方面的最新进展,这些进展源自关键临床试验SPARTAN、PROSPER和ARAMIS,以支持临床医生对这些患者进行最佳管理。值得注意的是,新型、更精确的新一代成像技术(包括镓前列腺特异性膜抗原正电子发射断层扫描/CT)以及最终可能出现的未来肿瘤生物标志物的出现,正在改变nmCRPC情况的实体和定义,从而对患者的诊断和管理产生影响。