Nilsson Sten
Department of Oncology-Pathology, Karolinska University Hospital, Karolinska Institutet, SE-17177, Solna, Sweden.
Curr Oncol Rep. 2016 Feb;18(2):14. doi: 10.1007/s11912-015-0495-4.
Metastatic castration-resistant prostate cancer (mCRPC) frequently metastasizes to the bone, often resulting in painful skeletal events, reduced quality of life, and reduced survival. The beta-emitting radiopharmaceuticals strontium-89 and samarium-153 alleviated pain in mCRPC patients with widespread skeletal metastases and have been associated with myelotoxicity. Radium-223, a first-in-class alpha-emitting radiopharmaceutical, prolonged overall survival, delayed symptomatic skeletal events, and improved quality of life, versus placebo, in patients with CRPC and symptomatic bone metastases and no visceral metastases. Radium-223 provided survival benefit to patients with CRPC and symptomatic bone metastases, regardless of prior docetaxel use. Importantly, prostate-specific antigen level and pain palliation were not a measure of radium-223 treatment response and should not alter the decision to administer all six radium-223 injections, the recommended regimen for survival benefit. Radium-223 was generally well tolerated, leading to ongoing clinical trials in combination with other therapeutics. Thus, radium-223 is a valuable addition to the mCRPC treatment armamentarium.
转移性去势抵抗性前列腺癌(mCRPC)常转移至骨骼,常导致疼痛性骨事件、生活质量下降及生存期缩短。发射β射线的放射性药物锶-89和钐-153可缓解广泛骨转移的mCRPC患者的疼痛,但与骨髓毒性有关。镭-223是首个发射α射线的放射性药物,与安慰剂相比,可延长去势抵抗性前列腺癌(CRPC)伴症状性骨转移且无内脏转移患者的总生存期,延迟症状性骨事件发生,并改善生活质量。无论之前是否使用多西他赛,镭-223均可使CRPC伴症状性骨转移患者获益。重要的是,前列腺特异性抗原水平和疼痛缓解情况并非镭-223治疗反应的衡量指标,不应改变给予全部六次镭-223注射(为获得生存获益的推荐方案)的决定。镭-223总体耐受性良好,从而引发了其与其他疗法联合应用的临床试验。因此,镭-223是mCRPC治疗手段中的一项重要补充。