Molecular Health GmbH, Heidelberg, Germany.
Department of Nuclear Medicine, Aristotle University of Thessaloniki, Papageorgiou Hospital, Thessaloniki, Greece.
Medicina (Kaunas). 2019 May 16;55(5):149. doi: 10.3390/medicina55050149.
: Radium-223 dichloride (Xofigo®) is a calcium mimetic agent approved for the treatment of castration-resistant prostate cancer patients with symptomatic bone metastases and no known visceral metastatic disease. This targeted, α-particle-emitting therapy has demonstrated significant survival benefit accompanied by a favorable safety profile. Nevertheless, recent evidence suggests that its combined use with abiraterone and prednisone/prednisolone may be associated with increased risk of death and fractures. While the precise pathophysiologic mechanisms of these events are not yet clear, collecting evidence from more clinical trials and translational studies is necessary. The aim of our present study is to assess whether accessible sources of patient outcome data can help gain additional clinical insights to radium-223 dichloride's safety profile. : We performed a retrospective analysis of cases extracted from the FDA Adverse Event Reporting System and characterized side effect occurrence by using reporting ratios. Results: A total of ~1500 prostate cancer patients treated with radium-223 dichloride was identified, and side effects reported with the use of radium-223 dichloride alone or in combination with other therapeutic agents were extracted. Our analysis demonstrates that radium-223 dichloride may often come with hematological-related reactions, and that, when administered together with other drugs, its safety profile may differ. Conclusions: While more prospective studies are needed to fully characterize the toxicological profile of radium-223 dichloride, the present work constitutes perhaps the first effort to examine its safety when administered alone and in combination with other agents based on computational evidence from public real-world post marketing data.
镭-223 二氯化物(Xofigo®)是一种钙模拟剂,被批准用于治疗有症状的骨转移且无已知内脏转移疾病的去势抵抗性前列腺癌患者。这种靶向、α 粒子发射疗法已显示出显著的生存获益,并具有良好的安全性。然而,最近的证据表明,它与阿比特龙联合使用可能会增加死亡和骨折的风险。虽然这些事件的确切病理生理机制尚不清楚,但需要从更多的临床试验和转化研究中收集证据。我们目前的研究旨在评估可获得的患者结局数据来源是否有助于更深入地了解镭-223 二氯化物的安全性。
我们对从 FDA 不良事件报告系统中提取的病例进行了回顾性分析,并使用报告比值来描述副作用的发生情况。结果:共确定了约 1500 例接受镭-223 二氯化物治疗的前列腺癌患者,并提取了单独使用镭-223 二氯化物或与其他治疗药物联合使用时报告的副作用。我们的分析表明,镭-223 二氯化物可能经常引起血液相关反应,并且当与其他药物联合使用时,其安全性可能会有所不同。结论:虽然需要更多的前瞻性研究来充分描述镭-223 二氯化物的毒理学特征,但本工作可能是首次根据公共真实世界上市后数据的计算证据,单独和联合其他药物使用时检查其安全性的努力。