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. 2013 May 22;8(5):e64275.
doi: 10.1371/journal.pone.0064275. Print 2013.

Therapeutic options in docetaxel-refractory metastatic castration-resistant prostate cancer: a cost-effectiveness analysis

Affiliations

Therapeutic options in docetaxel-refractory metastatic castration-resistant prostate cancer: a cost-effectiveness analysis

Lixian Zhong et al. PLoS One. .

Abstract

Background: Docetaxel is an established first-line therapy to treat metastatic castration-resistant prostate cancer (mCRPC). Recently, abiraterone and cabazitaxel were approved for use after docetaxel failure, with improved survival. National Institute for Health and Clinical Excellence (NICE) preliminary recommendations were negative for both abiraterone (now positive in final recommendation) and cabazitaxel (negative in final recommendation).

Objective: To evaluate the cost-effectiveness of abiraterone, cabazitaxel, mitoxantrone and prednisone for mCRPC treatment in US.

Methods: A decision-tree model was constructed to compare the two mCRPC treatments versus two placebos over 18 months from a societal perspective. Chance nodes include baseline pain as a severity indicator, grade III/IV side-effects, and survival at 18 months. Probabilities, survival and health utilities were from published studies. Model cost inputs included drug treatment, side-effect management and prevention, radiation for pain, and death associated costs in 2010 US dollars.

Results: Abiraterone is a cost-effective choice at $94K/QALY (quality adjusted life years) compared to placebo in our base-case analysis. Cabazitaxel and abiraterone are the most effective, yet also most expensive agents. The incremental cost-effectiveness ratios (ICER) at base-case are $101K/QALY (extended dominated) for mitoxantrone vs. placebo, $91K/QALY for abiraterone vs. mitoxantrone, $956K/QALY for cabazitaxel vs. abiraterone. Abiraterone becomes less cost-effective as its AWP increases, or if the cost of mitoxantrone side-effect management decreases. Increases in the percentage of patients with baseline pain leads to an increased ICER for both mitoxantrone and abiraterone, but mitoxantrone does relatively better. Cabazitaxel remains not cost-effective.

Conclusion: Our base case model suggests that abiraterone is a cost-effective option in docetaxel-refractory mCRPC patients. Newer treatments will also need a CEA assessment compared to abiraterone.

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Conflict of interest statement

Competing Interests: The authors have no conflict of interests to disclose.

Figures

Figure 1
Figure 1. Decision Tree Structure.
Decision tree model was constructed for the comparison of cost-effectiveness of two treatment options: abiraterone and cabazitaxel against two placebo ground: prednisone a lone and mitoxantrone for mCRPC patients who have failed prior docetaxel treatment. Chance node branches of our base-case analysis included baseline pain, grade III/IV side-effects, and overall survival at 18 months.
Figure 2
Figure 2. Cost-effectiveness Efficiency Frontier.
*Ext. Dom. =  Extended Dominance: Mitoxantrone show extended dominance indicating that some combination of Abiraterone and Prednisone would be preferable to treating all with mitoxantrone. **Cost is in US 2010 $s; Effectiveness is in quality adjusted life years (QALYs).
Figure 3
Figure 3. Cost-Effectiveness Acceptance Curve.
Probabilistic sensitivity analysis was conducted to derive CE acceptance curve (seed: 1234).

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Grants and funding

This study is unfunded. Thus, the funders had no roles in study design, data collection and analysis, decision to publish or preparation of the manuscript.