Abstract

Background:National Comprehensive Cancer Network guidelines recommend monthly osteoclast inhibitor treatment (OIT) in men with metastatic castration-resistant prostate cancer (mCRPC) to prevent skeletal related events (SREs). We assessed adherence to guidelines by quantifying treatment for SRE prevention in a population-based cohort of men with mCRPC.Methods:Using Surveillance, Epidemiology, and End Results-Medicare data, we identified men aged >65 with prostate cancer as a primary cause of death during 2006–2010. We assessed OIT during a 12-month period between 15 and 3 months before death and used multivariable negative binomial regression to identify factors associated with treatment.Results:Among 9,634 men who died of prostate cancer, 22% received ≥ 1 OIT, and use increased slightly over time. Men age 75–84 and ≥ 85 were less likely than younger men to be treated (IRR 0.63, 95% CI 0.49–0.78 and IRR 0.34, 95% CI 0.17–0.50, respectively). African American men were less likely than white men to receive OIT (IRR 0.75, 95% CI 0.54–0.95), as were men from areas with lower median income (P=0.014). Compared with men seeing a urologist only, men seeing a medical oncologist and a urologist (IRR 2.52, 95% CI 2.36–2.68) or a medical oncologist alone (IRR 3.82, 95% CI 3.54–4.09) had higher incidence rates of treatment.Conclusions:Fewer than a quarter of American men dying of prostate cancer received recommended treatment to prevent SREs within the final year of their lives, with particularly low rates of treatment among older men, African American men, and those living in areas with low median income. Visits with a medical oncologist were associated with increased use. Further evaluation of these disparities by age, race and socioeconomic status are necessary to identify interventions to reduce them.

Highlights

  • Prostate cancer is the most common non-cutaneous malignancy among American men and is the second leading cause of cancer death in the United States [1]

  • Men treated with ADT via orchiectomy or GnRH agonist were more likely to osteoclast inhibitor treatment (OIT) than men not treated with ADT, and men with osteoporosis were more likely to receive treatment than men without osteoporosis (IRR 3.18, 95% CI 3.04-3.31 for men treated with a GnRH agonist, IRR 1.83, 95% CI 1.44-2.23 for men treated with orchiectomy, and 1.24, 95% CI 1.05-1.44 for men with osteoporosis)

  • Guideline recommendations based on level one evidence suggest monthly treatment of men with metastatic castration-resistant prostate cancer (mCRPC) with OIT to prevent skeletal related events (SREs) and reduce morbidity and mortality in this population [14]

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Summary

Introduction

Prostate cancer is the most common non-cutaneous malignancy among American men and is the second leading cause of cancer death in the United States [1]. Osteoclast inhibitor treatment (OIT) reduces the risk of SRE, hospitalization, and mortality in men with prostate cancer [3]. We assessed rate of treatment with OIT in a large, population-based cohort of older American men with prostate cancer during a 12-month period beginning 15 months before death and concluding 3 months before death from prostate cancer. National Comprehensive Cancer Network guidelines recommend monthly osteoclast inhibitor treatment (OIT) in men with metastatic castration-resistant prostate cancer (mCRPC) to prevent skeletal related events (SREs). Conclusions: Fewer than a quarter of American men dying of prostate cancer received recommended treatment to prevent SREs within the final year of their lives, with low rates of treatment among older men, African American men, and those living in areas with low median income. Further evaluation of these disparities by age, race and socioeconomic status are necessary to identify interventions to reduce them

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