McGann Shane, Horton Evan R
MCPHS University, Boston, MA, USA Genzyme, A Sanofi Company, Cambridge, MA, USA
MCPHS University, Boston, MA, USA.
Ann Pharmacother. 2015 Apr;49(4):469-76. doi: 10.1177/1060028014565444. Epub 2015 Jan 8.
To review and evaluate the clinical trial efficacy and safety of radium 223 ((223)Ra) along with its place in therapy in men with castration-resistant prostate cancer (CRPC).
A literature search in PubMed/MEDLINE (up to October 2014) was performed using various combinations of the terms radium, hormone-refractory prostate cancer, and castration-resistant prostate cancer. The New Drug Application Medical, Pharmacology, and Clinical Pharmacology and Biopharmaceutics Reviews for radium (223)Ra dichloride were also utilized. The bibliographies of articles were reviewed to identify additional references.
Phase 1, 2, and 3 studies that assessed the safety and/or efficacy of (223)Ra in patients with CRPC were reviewed. Peer-reviewed articles with clinically relevant information were reviewed for background information.
In May 2013, the Food and Drug Administration approved intravenous use of (223)Ra for the treatment of patients with CRPC, symptomatic bone metastases, and no known visceral metastatic disease. In a phase 3 study comparing (223)Ra and the best standard of care (SOC) versus the best SOC plus placebo, (223)Ra was shown to increase survival. The most commonly seen adverse drug reactions and hematological laboratory abnormalities with (223)Ra include nausea, diarrhea, vomiting, peripheral edema, anemia, lymphocytopenia, leukopenia, thrombocytopenia, and neutropenia.
(223)Ra is a first-in-class α-particle-emitting radioactive agent that is first-line therapy, providing an extra option for men suffering from CRPC with symptomatic bone metastases and no known visceral metastases. (223)Ra has also been shown to be relatively well tolerated when up to 6 injections are given. Further studies are needed to evaluate whether (223)Ra is safe and effective for more than 6 doses and if it can be used concomitantly with chemotherapy.
回顾并评估镭-223(²²³Ra)治疗去势抵抗性前列腺癌(CRPC)男性患者的临床试验疗效、安全性及其在治疗中的地位。
在PubMed/MEDLINE数据库(截至2014年10月)中,使用镭、激素难治性前列腺癌和去势抵抗性前列腺癌等术语的各种组合进行文献检索。还利用了二氯化镭(²²³Ra)的新药申请医学、药理学、临床药理学和生物药剂学综述。对文章的参考文献进行回顾以识别其他参考文献。
对评估²²³Ra在CRPC患者中的安全性和/或疗效的1、2、3期研究进行了回顾。对具有临床相关信息的同行评审文章进行回顾以获取背景信息。
2013年5月,美国食品药品监督管理局批准静脉使用²²³Ra治疗CRPC、有症状骨转移且无已知内脏转移疾病的患者。在一项3期研究中,比较了²²³Ra与最佳标准治疗(SOC)以及最佳SOC加安慰剂,结果显示²²³Ra可提高生存率。²²³Ra最常见的药物不良反应和血液学实验室异常包括恶心、腹泻、呕吐、外周水肿、贫血、淋巴细胞减少、白细胞减少、血小板减少和中性粒细胞减少。
²²³Ra是一流的发射α粒子的放射性药物,为患有有症状骨转移且无已知内脏转移的CRPC男性患者提供了一线治疗的额外选择。当给予多达6次注射时,²²³Ra的耐受性也相对较好。需要进一步研究以评估²²³Ra超过6剂时是否安全有效,以及它是否可与化疗联合使用。