COMPARATIVE ANALYSIS OF RADIUM-223 VS. PLACEBO IN SYMPTOMATIC METASTATIC CASTRATION RESISTANT PROSTATE CANCER TREATED WITH BEST STANDARD OF CARE ON SKELETAL-RELATED EVENTS OUTCOMES

Author(s)

Seal B*1;Pawar V2;Valderrama A3;Grabbi E4;Lloyd A4, Beaudet A5 1Bayer HealthCare Pharmaceuticals, Inc., Pine Brook, NJ, USA, 2Bayer Healthcare Pharmaceuticals, Montville, NJ, USA, 3Bayer, Cedar Grove, NJ, USA, 4IMS Health, London, United Kingdom, 5IMS Health, Basel, Switzerland

OBJECTIVES: Radium-223 dichloride (Ra-223) is a novel alpha-radiopharmaceutical, which delayed time to first skeletal-related event (SRE) and improved overall survival versus best standard of care (BSoC) in patients with symptomatic castration-resistant prostate cancer (mCRPC) with bone metastases. This analysis evaluated economic benefits associated with Ra-223. METHODS: A Markov model was developed using patient-level data from a pivotal trial in which mCRPC patients receiving BSoC were randomized 2:1 to Ra-223 or placebo respectively. Patients entered the model progression-free, receiving active treatment until progression or completion of the therapy course. Health states reflected patients experiencing first or subsequent SRE.  In the trial, SRE was defined as treatment with external-beam radiation therapy (EBRT), surgical intervention, occurrence of pathological bone fracture, or spinal cord compression. A 5-year time horizon was considered. Costs were estimated from a US payer perspective. SRE costs were obtained by multiplying the number of patients experiencing SRE by its specific treatment cost (including hospitalization costs). RESULTS: Ra-223 increased mean life expectancy by 0.325 (95% CI: 0.324-0.326) years in the ITT population and 0.517 (95% CI: 0.516-0.518) years in the subgroup of patients who had not received first-line docetaxel. Ra-223 was projected to lead to 44% reduction in the cost of treatment of SREs versus BSC: 46% reduction in pathologic bone fracture costs; 48% for spinal cord compression; 16% for external beam radiation; and 11% for surgical interventions. A total of 32.9% of patients suffered a first SRE for Ra-223 versus 37.8% for placebo and 6.5% and 7.8%, respectively, suffered two or more SRE events. CONCLUSIONS: In patients treated with BSoC, Ra-223 reduced costs of SREs. Future studies will evaluate the total cost of care related to the benefit of Ra-223 versus placebo in patients treated with BSoC in mCRPC once the cost of therapy and the impact on quality adjusted survival are known.

Conference/Value in Health Info

2013-05, ISPOR 2013, New Orleans, LA, USA

Value in Health, Vol. 16, No. 3 (May 2013)

Code

PCN35

Topic

Economic Evaluation

Topic Subcategory

Cost-comparison, Effectiveness, Utility, Benefit Analysis

Disease

Oncology

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