| Literature DB >> 29046247 |
Tai-Lung Cha1, Tony Tong-Lin Wu2, Nicholas John Vogelzang3, Chao-Yuan Huang4, Shu-Pin Huang5, Chia-Chi Lin6, Yen-Chuan Ou7, See-Tong Pang8, Daniel Heung-Yuan Shen9, Wen-Jeng Wu10, Wayne Yen-Hwa Chang11.
Abstract
Radium-223 is a first-in-class α-emitting radiopharmaceutical that targets bone metastases associated with metastatic castration-resistant prostate cancer (mCRPC). In the pivotal phase III trial ALSYMPCA, radium-223 significantly increased overall survival (OS), compared with placebo (median 14.9 vs 11.3 months; hazard ratio 0.70; 95% CI 0.58-0.83; p < 0.001), in patients with mCRPC and symptomatic bone metastases-with a comparable safety profile. To optimize treatment outcomes, selection of appropriate patients is important. As well as osteoblastic bone metastases, mCRPC patients should be well enough to receive six doses of radium-223 as this treatment duration has been shown to greatly improve OS outcomes compared with administration of four or fewer doses. Additionally, alkaline phosphatase and lactate dehydrogenase are emerging as important biomarkers during radium-223 treatment. Optimal concomitant standard-of-care therapies (such as abiraterone or enzalutamide) to be administered with radium-223 have yet to be defined as does the most efficacious dose and duration of radium-223 treatment. In conclusion, radium-223 is an important addition to the mCRPC treatment landscape and marks a paradigm shift in the treatment of bone metastases.Entities:
Keywords: Castration-resistant prostate cancer; Osteoblasts; Radiopharmaceuticals; Radium chloride Ra 223
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Year: 2017 PMID: 29046247 DOI: 10.1016/j.jfma.2017.04.005
Source DB: PubMed Journal: J Formos Med Assoc ISSN: 0929-6646 Impact factor: 3.282