H-5 ARE THERE GAINS IN COST-EFFECTIVENESS OF CHEMOPREVENTION FOR PROSTATE CANCER WHEN TARGETING MEN AT HIGHER RISK BASED ON FAMILY HISTORY AND GENETIC RISK MARKERS?

Tuesday, October 26, 2010: 11:15 AM
Grand Ballroom West (Sheraton Centre Toronto Hotel)
Shelby D. Reed, PhD1, Charles D. Scales Jr., MD2, Suzanne B. Stewart, MD2, Judd W. Moul, MD2, Jielin Sun, PhD3, Kevin A. Schulman, MD1 and Jianfeng Xu, PhD3, (1)Duke Clinical Research Institute, Durham, NC, (2)Duke University Medical Center, Durham, NC, (3)Wake Forest University School of Medicine, Winston-Salem, NC

Purpose:   Targeted strategies for chemoprevention of prostate cancer with finasteride toward higher risk groups could be more cost-effective than untargeted chemoprevention.   Recently published risk prediction models by Xu et al. can predict a man's risk of prostate cancer as a function of family history and 14 genetic markers.  In this study, we estimated the cost-effectiveness of chemoprevention strategies across risk groups defined by family history and number of inherited risk alleles.

Method:   We developed a probabilistic Markov model with 8 health states using data from SEER databases, US life tables, the published medical literature and other on-line sources to estimate costs and quality-adjusted survival to model the impact of chemoprevention with finasteride on the prevention of prostate cancer.  We incorporated a decision tree to integrate the prevalence of different risk groups based on family history and genetic risk factors to evaluate the cost-effectiveness of various prevention strategies. 

Result:   In men 50 years of age, chemoprevention with finasteride for 25 years is estimated to increase (discounted) quality-adjusted life expectancy by 0.101 QALYs (95% CI: 0.006-0.151) at an incremental (discounted) cost of $9,043 (95% CI: 8,549-9,498) relative to no chemoprevention; an incremental cost-effectiveness ratio of $89,300 per QALY (95% CI, 58,800-149,800).  Among men with a negative family history, the cost-effectiveness of chemoprevention ranged from $128,600 per QALY (95% CI; 78,000-248,700) in men with 7 or fewer risk alleles to $65,200/QALY (95% CI: 43,900-114,800) in men with 14 or more risk alleles.  Across all men with a positive family history (and no genetic testing), the cost-effectiveness of chemoprevention was estimated at $64,200 per QALY.  At an estimated cost of $400 per individual with a negative family history, the cost-effectiveness of targeting chemoprevention based on genetic information ranged from $98,100 per QALY when restricting chemoprevention to men with 14 or more risk alleles to $103,200 per QALY when expanding chemoprevention to men with 8 or more risk alleles.

Conclusion:   In men with a negative family history of prostate cancer, there was little gain in cost-effectiveness when targeting chemoprevention to men on the basis of this set of genetic risk factors.