Objective. To examine prostate cancer trends by demographic and tumor characteristics because a comprehensive examination of recent prostate cancer incidence rates is lacking. Patients and Methods. We described prostate cancer incidence rates and trends using the 2001–2007 National Program of Cancer Registries and Surveillance, Epidemiology, and End Results Program data (representing over 93% of US population). Because of coding changes in cancer grade, we restricted analysis to 2004–2007. We conducted descriptive and trend analyses using SEER*Stat. Results. The overall prostate cancer incidence rate was stable from 2001 to 2007; however, rates significantly increased among men aged 40–49 years (APC = 3.0) and decreased among men aged 70–79 years (APC = 2.3), and 80 years or older (APC = ?4.4). About 42% of localized prostate cancers diagnosed from 2004 to 2007 were poorly differentiated. The incidence of poorly differentiated cancer significantly increased among localized (APC = 8.0) and regional stage (APC = 6.1) prostate cancers during 2004–2007. Conclusions. The recent trend in prostate cancer incidence was stable but varied dramatically by age. Given the large proportion of poorly differentiated disease among localized prostate cancers and its increasing trend in more recent years, continued monitoring of prostate cancer incidence and trends by demographic and tumor characteristics is warranted. 1. Introduction Prostate cancer is the most commonly diagnosed non-skin cancer and the second leading cause of cancer death among American men. Each year, approximately 220,000 men are diagnosed with prostate cancer and 29,000 die from it [1]. With the introduction of the prostate-specific antigen (PSA) testing in the mid-1980s, prostate cancer incidence rate increased drastically, at about 12% per year, and peaked in 1992 [2]. The rate subsequently declined, at about 10% per year for the following three years and then appeared to stabilize from 1995 to 2005 [2, 3]. In 2011, Kohler et al. reported a stable trend of prostate cancer incidence from 1998 to 2007; however, demographic and clinical factors were not examined in this study [4]. With the widespread use of the PSA test, the mean age at diagnosis dropped substantially, from 72.2 years between 1988-1989 to 67.2 years between 2004 and 2005 [5]. Studies using Surveillance, Epidemiology, and End Results Program (SEER) data have shown that the distribution of prostate cancer stage and grade has also dramatically changed, with localized and moderately differentiated tumors becoming predominant [6, 7]. Age
References
[1]
U.S. Cancer Statistics Working Group, United States Cancer Statistics: 1999–2006 Incidence and Mortality Web-Based Report, U.S. Department of Health and Human Services, Centers for Disease Control and Prevention and National Cancer Institute, Atlanta, Ga, USA, 2010.
[2]
J. L. Stanford, R. A. Stephenson, L. M. Coyle et al., “Prostate Cancer Trends 1973–1995, SEER Program, National Cancer Institute,” NIH 99-4543, Bethesda, Md, USA, 1999.
[3]
H. G. Welch and P. C. Albertsen, “Prostate cancer diagnosis and treatment after the introduction of prostate-specific antigen screening: 1986–2005,” Journal of the National Cancer Institute, vol. 101, no. 19, pp. 1325–1329, 2009.
[4]
B. A. Kohler, E. Ward, B. J. McCarthy et al., “Annual report to the nation on the status of cancer, 1975–2007, featuring tumors of the brain and other nervous system,” Journal of the National Cancer Institute, vol. 103, no. 9, pp. 714–736, 2011.
[5]
Y. H. Shao, K. Demissie, W. Shih et al., “Contemporary risk profile of prostate cancer in the United States,” Journal of the National Cancer Institute, vol. 101, no. 18, pp. 1280–1283, 2009.
[6]
A. B. Jani, P. A. S. Johnstone, S. L. Liauw, V. A. Master, and O. W. Brawley, “Age and grade trends in prostate cancer (1974–2003): a surveillance, epidemiology, and end results registry analysis,” American Journal of Clinical Oncology, vol. 31, no. 4, pp. 375–378, 2008.
[7]
R. A. Stephenson, “Prostate cancer trends in the era of prostate-specific antigen an update of incidence, mortality, and clinical factors from the SEER database,” Urologic Clinics of North America, vol. 29, no. 1, pp. 173–181, 2002.
[8]
A. B. Jani and S. Hellman, “Early prostate cancer: clinical decision-making,” The Lancet, vol. 361, no. 9362, pp. 1045–1053, 2003.
[9]
B. F. Hankey, L. A. Ries, and B. K. Edwards, “The surveillance, epidemiology, and end results program: a national resource,” Cancer Epidemiology Biomarkers and Prevention, vol. 8, no. 12, pp. 1117–1121, 1999.
[10]
P. A. Wingo, P. M. Jamison, R. A. Hiatt et al., “Building the infrastructure for nationwide cancer surveillance and control—a comparison between The National Program of Cancer Registries (NPCR) and The Surveillance, Epidemiology, and End Results (SEER) Program (United States),” Cancer Causes and Control, vol. 14, no. 2, pp. 175–193, 2003.
[11]
A. Fritz, C. Percy, A. Jack, et al., International Classification of Disease for Oncology, World Health Organization, Geneva, Switzerland, 2000.
[12]
C. H. Johnson, Ed., “SEER Program Coding and Staging Manual 2004, Revision 1. National Cancer Institute,” NIH 04-5581, Bethesda, Md, USA, 2004.
[13]
R. M. Merrill and A. Sloan, “Risk-adjusted incidence rates for prostate cancer in the United States,” Prostate, vol. 72, no. 2, pp. 181–185, 2012.
[14]
A. M. D. Wolf, R. C. Wender, R. B. Etzioni et al., “American Cancer Society guideline for the early detection of prostate cancer: update 2010,” CA Cancer Journal for Clinicians, vol. 60, no. 2, pp. 70–98, 2010.
[15]
“Screening for prostate cancer. American College of Physicians,” Annals of Internal Medicine, vol. 126, no. 6, pp. 480–484, 1997.
[16]
“Prostate-specific antigen (PSA) best practice policy. American Urological Association (AUA),” Oncology, vol. 14, pp. 267–280, 2000.
[17]
L. S. Lim and K. Sherin, “Screening for prostate cancer in U.S. men ACPM position statement on preventive practice,” American Journal of Preventive Medicine, vol. 34, no. 2, pp. 164–170, 2008.
[18]
M. W. Drazer, D. Huo, M. A. Schonberg, A. Razmaria, and S. E. Eggener, “Population-based patterns and predictors of prostate-specific antigen screening among older men in the United States,” Journal of Clinical Oncology, vol. 29, no. 13, pp. 1736–1743, 2011.
[19]
J. Li, R. German, J. King et al., “Recent trends in prostate cancer testing and incidence among men under age of 50,” Cancer Epidemiology, vol. 36, no. 2, pp. 122–127, 2012.
[20]
P. C. Albertsen, J. A. H. Hanley, G. H. Barrows et al., “Prostate cancer and the Will Rogers phenomenon,” Journal of the National Cancer Institute, vol. 97, no. 17, pp. 1248–1253, 2005.
[21]
J. I. Epstein, W. C. Allsbrook, M. B. Amin et al., “The 2005 International Society of Urological Pathology (ISUP) consensus conference on Gleason grading of prostatic carcinoma,” American Journal of Surgical Pathology, vol. 29, no. 9, pp. 1228–1242, 2005.
[22]
D. W. Lin, M. Porter, and B. Montgomery, “Treatment and survival outcomes in young men diagnosed with prostate cancer: a population-based cohort study,” Cancer, vol. 115, no. 13, pp. 2863–2871, 2009.
[23]
M. R. Cooperberg, J. M. Broering, and P. R. Carroll, “Time trends and local variation in primary treatment of localized prostate cancer,” Journal of Clinical Oncology, vol. 28, no. 7, pp. 1117–1123, 2010.
[24]
R. Chou, J. M. Croswell, T. Dana et al., “Screening for prostate cancer: a review of the evidence for the U.S. Preventive Services Task Force,” Annals of Internal Medicine, vol. 155, pp. 762–771, 2011.