Mollica Veronica, Rizzo Alessandro, Rosellini Matteo, Marchetti Andrea, Ricci Angela Dalia, Cimadamore Alessia, Scarpelli Marina, Bonucci Chiara, Andrini Elisa, Errani Costantino, Santoni Matteo, Montironi Rodolfo, Massari Francesco
Division of Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Via Albertoni 15, 40138 Bologna, Italy.
Section of Pathological Anatomy, School of Medicine, United Hospitals, Polytechnic University of the Marche Region, 60121 Ancona, Italy.
Cancers (Basel). 2021 Feb 1;13(3):546. doi: 10.3390/cancers13030546.
Bone health represents a major issue in castration-resistant prostate cancer (CRPC) patients with bone metastases; in fact, the frequently prolonged use of hormonal agents causes important modifications in physiological bone turnover and most of these men will develop skeletal-related events (SREs), including spinal cord compression, pathologic fractures and need for surgery or radiation to bone, which are estimated to occur in almost half of this patient population. In the last decade, several novel therapeutic options have entered into clinical practice of bone metastatic CRPC, with recent approval of enzalutamide and abiraterone acetate, cabazitaxel chemotherapy and radium-223, on the basis of survival benefit suggested by landmark Phase III trials assessing these agents in this setting. Conversely, although bone-targeted agents (BTAs)-such as the bisphosphonate zoledronic acid and the receptor activator of nuclear factor kappa-B (RANK) ligand inhibitor denosumab-are approved for the prevention of SREs, these compounds have not shown benefit in terms of overall survival. However, emerging evidence has suggested that the combination of BTAs and abiraterone acetate, enzalutamide and the radiopharmaceutical radium-223 could result in improved clinical outcomes and prolonged survival in bone metastatic CRPC. In this review, we will provide an overview on bone tropism of prostate cancer and on the role of BTAs in metastatic hormone-sensitive and castration-resistant prostate cancer.
骨健康是去势抵抗性前列腺癌(CRPC)骨转移患者面临的一个主要问题;事实上,激素药物的频繁长期使用会导致生理性骨转换发生重要改变,并且这些男性中的大多数会发生骨骼相关事件(SREs),包括脊髓压迫、病理性骨折以及需要进行骨手术或放疗,据估计几乎一半的该患者群体都会出现这些情况。在过去十年中,一些新型治疗方案已进入骨转移CRPC的临床实践,基于在该背景下评估这些药物的具有里程碑意义的III期试验所显示的生存获益,恩杂鲁胺、醋酸阿比特龙、卡巴他赛化疗和镭 - 223最近获得批准。相反,尽管骨靶向药物(BTAs)——如双膦酸盐唑来膦酸和核因子κB受体激活剂(RANK)配体抑制剂地诺单抗——被批准用于预防SREs,但这些化合物在总生存方面并未显示出获益。然而,新出现的证据表明,BTAs与醋酸阿比特龙、恩杂鲁胺以及放射性药物镭 - 223联合使用可能会改善骨转移CRPC的临床结局并延长生存期。在这篇综述中,我们将概述前列腺癌的骨嗜性以及BTAs在转移性激素敏感性和去势抵抗性前列腺癌中的作用。