Elsevier

European Urology

Volume 71, Issue 2, February 2017, Pages 195-201
European Urology

Platinum Priority – Prostate Cancer
Editorial by Jennifer R. Rider on pp. 202–203 of this issue
Trends in the Incidence of Fatal Prostate Cancer in the United States by Race

https://doi.org/10.1016/j.eururo.2016.05.011Get rights and content

Abstract

Background

Prostate-specific antigen (PSA) testing has dramatically changed the composition of prostate cancer (PCa), making it difficult to interpret incidence trends. New methods are needed to examine temporal trends in the incidence of clinically significant PCa and whether trends vary by race.

Objective

To conduct an in-depth analysis of incidence trends in clinically significant PCa, defined as cases in which PCa was the underlying cause of death within 10 yr of diagnosis.

Design, setting, and participants

We extracted incident PCa cases during the period 1975–2002 and associated causes of death and survival through 2012 from nine cancer registries in the population-based Surveillance Epidemiology and End Results program database.

Outcome measurements and statistical analysis

We applied joinpoint regression analysis to identify when significant changes in trends occurred and age–period–cohort models to examine longitudinal and cross-sectional trends in the incidence of fatal PCa.

Results and limitations

Among 51 680 fatal PCa cases, incidence increased 1% per year prior to 1992, declined 15% per year from 1992 to 1995, and further declined by 5% per year through 2002. Age-specific incidence rates of fatal disease decreased >2% per year among men aged ≥60 yr, yet rates remained relatively stable among men aged ≤55 yr. Fatal disease rates were >2-fold higher in black men compared with white men, a racial disparity that increased to 4.2-fold among younger men.

Conclusions

The incidence of fatal PCa substantially declined after widespread PSA screening and treatment advances. Nevertheless, rates of fatal disease among younger men have remained relatively stable, suggesting the need for additional attention to early onset PCa, especially among black men. The persistent black-to-white racial disparity observed in fatal PCa underscores the need for greater understanding of the causes of this difference so that strategies can be implemented to eliminate racial disparities.

Patient summary

We assessed how the incidence of ultimately fatal prostate cancer (PCa) changed over time. We found that the incidence of fatal PCa declined by >50% since the introduction of prostate-specific antigen testing and advances in treatment options; however, incidence rates among younger men remained relatively stable, and younger black men exhibited a 4.2-fold higher risk for fatal disease compared with white men.

Introduction

Prostate cancer (PCa) is the most frequently diagnosed cancer among men in the United States, with 180 890 new cases estimated for 2016 [1]. Despite notable improvements in PCa mortality rates in the United States over the past few decades [2], it is estimated that 26 120 men (8% of male cancer deaths) will die from this disease in 2016 [1]. Racial disparities in PCa are higher than for any other malignancy, with black men exhibiting a 2.5-fold greater risk of death from PCa compared with white men [1], [3].

There has been a substantial increase in PCa incidence rates in the United States over the past few decades largely due to the increased detection of asymptomatic disease, first through transurethral prostatectomy (TURP) for benign prostatic hyperplasia [4], followed by widespread prostate-specific antigen (PSA) testing beginning in 1986 [5], [6]. The subsequent decrease in PCa incidence rates, attributed to depletion of the latent PCa reservoir in the population, rendered the now-familiar “spike” in overall PCa incidence rates [6].

Accurate interpretation of clinically significant PCa incidence trends has been difficult because of the high prevalence of indolent disease and changes in screening practices. A majority of studies examining PCa trends have focused on the date of death (mortality rate) as opposed to the date of diagnosis [7], [8], which is a more applicable time metric for assessing disease trends during a period of clinical change. In addition, no study in the past decade examined trends using age–period–cohort analysis [9], likely because of unstable parameters resulting from the PCa incidence rate spike.

To overcome these problems and to provide an in-depth analysis of clinically significant PCa incidence trends and racial disparities, we assessed trends in the incidence of fatal PCa, defined as death from this disease within 10 yr of diagnosis [10].

Section snippets

Materials and methods

We obtained census population estimates, cancer incidence, mortality, and survival data for calendar years 1975 to 2012 from the National Cancer Institute's Surveillance Epidemiology and End Results (SEER) SEER-9 registries, which cover approximately 10% of the US population. We selected incident cases diagnosed with PCa (International Classification of Diseases for Oncology, third edition, code C619) as the first primary malignant cancer from 1975 (the first year all SEER-9 registries were

Results

Of the 309 289 men diagnosed with PCa during 1975–2002, fatal PCa accounted for 17% (n = 51 680) of the cases. A total of 222 321 men (72%) with PCa died from any cause during any period of follow-up, and 150 565 of those deaths (68%) occurred within 10 yr of PCa diagnosis. During the 10-yr period following diagnosis, PCa was the most common cause of death (34%), followed by ischemic heart disease (24%) and cerebrovascular diseases (5%).

Discussion

This study revealed a substantial decline in the incidence of fatal PCa among US men during the period 1975–2002, yet rates among younger men remained relatively stable over the study period. Our study showed that black men had substantially greater risk of fatal PCa than white men in every period and cohort examined, and this racial disparity was magnified among younger men.

Prior studies that examined trends in PCa mortality [7], [8], [9], [11], as opposed to incidence, are likely more

Conclusions

Incidence rates of fatal PCa in the United States have declined by >50% since the early 1990s, coinciding with diagnostic and treatment changes, yet rates among younger men have remained relatively stable. Robust risk-triaging strategies are needed to help further reduce PCa that ultimately results in fatal disease and to limit undue anxiety and overtreatment of men with PCa that will not progress. The racial disparity in fatal PCa persists, and the size of this disparity—particularly among

References (30)

  • R.L. Siegel et al.

    Cancer statistics, 2016

    CA Cancer J Clin

    (2016)
  • A.B. Ryerson et al.

    Annual Report to the Nation on the Status of Cancer, 1975–2012, featuring the increasing incidence of liver cancer

    Cancer

    (2016)
  • C. DeSantis et al.

    Cancer statistics for African Americans, 2013

    CA Cancer J Clin

    (2013)
  • R.M. Merrill et al.

    Role of transurethral resection of the prostate in population-based prostate cancer incidence rates

    Am J Epidemiol

    (1999)
  • T.A. Stamey et al.

    Prostate-specific antigen as a serum marker for adenocarcinoma of the prostate

    N Engl J Med

    (1987)
  • H.G. Welch et al.

    Prostate cancer diagnosis and treatment after the introduction of prostate-specific antigen screening: 1986–2005

    J Natl Cancer Inst

    (2009)
  • M.S. Wachtel et al.

    PSA screening and deaths from prostate cancer after diagnosisA population based analysis

    Prostate

    (2013)
  • R. Etzioni et al.

    Quantifying the role of PSA screening in the US prostate cancer mortality decline

    Cancer Causes Control

    (2008)
  • K.C. Chu et al.

    Trends in prostate cancer mortality among black men and white men in the United States

    Cancer

    (2003)
  • R.T. Vollmer

    The dynamics of death in prostate cancer

    Am J Clin Pathol

    (2012)
  • M.M. Epstein et al.

    Temporal trends in cause of death among Swedish and US men with prostate cancer

    J Natl Cancer Inst

    (2012)
  • H.J. Kim et al.

    Permutation tests for joinpoint regression with applications to cancer rates

    Stat Med

    (2000)
  • T.R. Holford

    The estimation of age, period and cohort effects for vital rates

    Biometrics

    (1983)
  • P.S. Rosenberg et al.

    Age-period-cohort models in cancer surveillance research: ready for prime time?

    Cancer Epidemiol Biomarkers Prev

    (2011)
  • R. Etzioni et al.

    The prostate cancer conundrum revisited: treatment changes and prostate cancer mortality declines

    Cancer

    (2012)
  • Cited by (76)

    • The Pursuit of Health Equity and Equality in Urologic Oncology: Where We Have Been and Where We Are Going

      2021, European Urology Focus
      Citation Excerpt :

      Other racial/ethnic minorities are affected by these disparities. Although the incidence of PCa is lower among Latinos, Asians, and Pacific Islanders than among White men, Latinos and some Asian subpopulations are more likely to be diagnosed at a later stage [13]. Native American/Alaska Native populations have a greater mortality-to-incidence ratio for numerous screen-detected cancers such as cervical, breast, prostate, and colorectal cancer [12].

    • Clinical-genomic Characterization Unveils More Aggressive Disease Features in Elderly Prostate Cancer Patients with Low-grade Disease

      2021, European Urology Focus
      Citation Excerpt :

      Third, the treatment and long-term follow-up outcomes were unavailable, limiting the ability to validate further Decipher score prognostic performance in these specific age groups. Fourth, data regarding patients’ race and relevant family history were unavailable, which are additional independent prognostic factors [41,42] unaccounted for in our analyses. Fifth, approximately a third of the clinical T category, NCCN risk group, and preoperative PSA data were missing, potentially confounding the results of the multivariable models.

    View all citing articles on Scopus
    View full text