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collects data from 40 urology practices in the United States (34 community based, 3
                                                                                         d
                       Veterans Administration [VA])-based and 3 academic center based).  Although
                       CaPSURE patients are broadly representative of prostate cancer diagnosed in the
                       community, patient selection is not based on a formal population sampling scheme.
                   •  The NCDB is an oncology outcomes database encompassing more than 1,500 cancer
                       programs in the U.S. (including Puerto Rico) accredited by the Commission on Cancer of
                                                                                         e
                       the American College of Surgeons and the American Cancer Society.
                   •  Other databases utilized by the primary studies were the Patterns of Care study
                       (sponsored by NCI and based on sampling participants through SEER) and the Los
                       Angeles County/University of Southern California (LAC/USC) Cancer Surveillance
                       Program (which is now a component registry of SEER).

                   In addition to the above databases, several studies obtained prostate cancer mortality data
               f rom the National Center for Health Statistics (NCHS) of the Centers for Disease Control and
                                                                                   f
               P revention (CDC), the U.S. principal health agency for vital statistics.
                                                                                                      th
                                                                                                  th
                   Included studies had large sample sizes (median sample size = 54,670 patients; 25 -75
               p ercentile 11,161-138,387), were published between 1990 and 2011, and analyzed data from
               1 969 to 2008. Figure 3 presents the years covered by each primary study and the databases used.
               A ppendix Tables C1.1-C1.14 present additional information about each of the studies relevant to
               K ey Question 1.
                   We organized the 79 studies into four groups, each of which is discussed in the following
               s ections:
                   1.  studies investigating trends in prostate cancer incidence
                   2.  studies investigating trends in prostate cancer mortality or survival
                   3.  studies investigating patient-, tumor-, or system-level characteristics at prostate cancer
                       diagnosis, and
                   4.  studies presenting information in treatment trends over time




























               d  See http://urology.ucsf.edu/clinicalres/CRuroOnc_gceps_capsure.html; last accessed September 30, 2011.
               e  See http://www.facs.org/cancer/ncdb/index.html; last accessed September 30, 2011.
               f  See http://www.cdc.gov/nchs/; last accessed September 30, 2011.



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