Miranda Jesus, Viñal David, Pinto Álvaro
Hospital Universitario La Paz. Madrid. Spain.
Arch Esp Urol. 2019 Jun;72(5):500-507.
The treatment of patients with metastatic castration-resistant prostate cancer (mCRPC) has evolved dramatically in the recent years with the approval of several new drugs. Together with other treatment modalities including chemotherapy, hormonal therapy and immunotherapy, radiopharmaceuticals have recently been incorporated to the therapeutic scenario of prostate cancer with the approval of Radium 223 dichloride (Ra-223) for the treatment of mCRPC patients with symptomatic bone metastasis and no visceral metastases. Radiopharmaceuticals have long been used for pain palliation in patients with bone metastases. However, the bone seeking properties and the favourable physical characteristic of alpha emitter radium 223 encouraged the clinical development of the drug, leading to survival advantage in the phase III trial ALSYMPCA. Now the efforts are directed to define the optimal patient selection and drug sequence. In this review, we will provide the best available evidence of mechanism of action, clinical data and future directions of Ra-223 in mCRPC.
近年来,随着几种新药的获批,转移性去势抵抗性前列腺癌(mCRPC)患者的治疗发生了巨大变化。除了化疗、激素治疗和免疫治疗等其他治疗方式外,随着二氯化镭223(Ra-223)获批用于治疗有症状骨转移且无内脏转移的mCRPC患者,放射性药物最近也被纳入前列腺癌的治疗方案中。放射性药物长期以来一直用于缓解骨转移患者的疼痛。然而,亲骨性特性以及α发射体镭223良好的物理特性推动了该药物的临床开发,使其在III期试验ALSYMPCA中具有生存优势。现在的努力方向是确定最佳的患者选择和用药顺序。在这篇综述中,我们将提供关于Ra-223在mCRPC中的作用机制、临床数据和未来方向的最佳现有证据。