Radium-223 for the treatment of castration-resistant prostate cancer

被引:11
|
作者
El-Amm, Joelle [1 ]
Aragon-Ching, Jeanny B. [1 ]
机构
[1] George Washington Univ, Med Ctr, Div Hematol & Oncol, Washington, DC 20037 USA
来源
ONCOTARGETS AND THERAPY | 2015年 / 8卷
关键词
prostate cancer; radiopharmaceuticals; bone metastases; radium-223; PAINFUL BONE METASTASES; PART II TREATMENT; DOUBLE-BLIND; SKELETAL COMPLICATIONS; SM-153; LEXIDRONAM; ZOLEDRONIC ACID; EMITTING RA-223; EAU GUIDELINES; SR-89; THERAPY; PHASE-III;
D O I
10.2147/OTT.S44291
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The vast majority of patients with metastatic castration-resistant prostate cancer (mCRPC) develop bone metastases. Bone metastases are a source of significant morbidity and affect quality of life in these patients. Several bone-targeting agents are approved for the treatment of bone metastases in prostate cancer, including bisphosphonates, denosumab, and radiopharmaceuticals. Radium-223 is a novel first-in-class alpha-emitting radiopharmaceutical that has been approved for treatment of patients with mCRPC with bone metastases. Radium-223 delivers cytotoxic radiation to the sites of bone metastases and offers the advantage of minimal myelosuppression. The landmark Phase III ALSYMPCA trial demonstrated that, in addition to providing bone-related palliation, radium-223 can also prolong overall survival in patients with mCRPC with bone metastases in the absence of visceral metastases and in the absence of lymphadenopathy greater than 3 cm. Ongoing trials will further elucidate its use in sequence or combination with other available therapies for mCRPC.
引用
收藏
页码:1103 / 1109
页数:7
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