Patient Selection for Radium-223 Therapy in Patients With Bone Metastatic Castration-Resistant Prostate Cancer: New Recommendations and Future Perspectives

被引:19
作者
van der Doelen, Maarten J. [1 ,2 ]
Mehra, Niven [2 ]
Hermsen, Rick [4 ]
Janssen, Marcel J. R. [3 ]
Gerritsen, Winald R. [2 ]
van Oort, Inge M. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Urol, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Radiol & Nucl Med, Nijmegen, Netherlands
[4] Canisius Wilhelmina Hosp, Dept Radiol & Nucl Med, Nijmegen, Netherlands
关键词
Alpha emitter; Molecular stratification; Overall survival; Prognostic variables; Radiopharmaceutical; PROGNOSTIC-FACTORS; DOUBLE-BLIND; OPEN-LABEL; SURVIVAL; DICHLORIDE; RA-223; PHASE-3; EXPERIENCE; ACCESS; SAFETY;
D O I
10.1016/j.clgc.2018.11.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radium-223 therapy was registered in 2013 as a new life-prolonging therapeutic option for patients with symptomatic bone metastatic castration-resistant prostate cancer after the phase 3 ALSYMPCA study. Postregistration reports on the use of radium-223 in real-world populations demonstrate that appropriate selection of patients for radium-223 therapy is challenging. While primarily retrospective and post hoc studies identified prognostic variables associated with overall survival, validated predictive biomarkers are still lacking. Important pretherapeutic prognostic variables include the number of prior therapies, baseline Eastern Cooperative Oncology Group performance status, baseline extent of bone metastatic disease, and baseline alkaline phosphatase, prostate-specific antigen, and lactate dehydrogenase levels. We reviewed the currently available literature to provide recommendations on patient selection for radium-223 therapy in patients with bone metastatic castration-resistant prostate cancer. In addition, the recent evidence from the report of the European Medicines Agency's Pharmacovigilance Risk Assessment Committee regarding the restricted use of radium-223 after interim data analysis of the ERA-223 trial has been incorporated into our recommendations. Future perspectives are also discussed, including radium-223 re-treatment, the use of concomitant therapies, and the implementation of pretherapeutic molecular analysis for treatment stratification. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:79 / 87
页数:9
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