Page 474 - An Evidence Review of Active Surveillance in Men With Localized Prostate Cancer
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Appendix Table C4.1. Descriptive characteristics of the randomized controlled trials and comparative cohort studies considered
                                        relevant to KQ4 (continued)
                                        Author, Year      Study name       Comparison       Study          Sample          Inclusion criteria                  Population description:             Quality
                                        [Pubmed ID]       /Database                         duration       size (total)                                        Age                                 Comments
                                                                                                                                                               PSA (ng/mL)
                                        Study design                                                                                                           Tumor grade
                                                                                                                                                               Stage
                                                                                b
                                        Thong 224         Eindhoven        “AS”  (long-     Mean 8 yr      142             All eligible patients diagnosed     Mean age at survey: “AS,” 75.8      B
                                        2009              Cancer           term                                            with prostate cancer between        yr; RT, 75.9 yr
                                        19747357          Registry         survivors) vs.                                  1994 and 1998 from ECR.                                                 Of 128 AS
                                                          (ECR)            EBRT(long-                                      Excluding persons who had died  PSA: NR                                 survivors,
                                        Retrospective                      term                                            before Nov. 1, 2004. For the                                            71 returned
                                        matched                            survivors)                                      purpose of this study, a sample     Grade: “AS,” TNM Grade 1,           survey
                                        cohort                                                                             of patients who would be            80.3%; TNM Grade 2, 19.7%.          (55%)
                                                                                                                           suitable for management with        RT, TNM Grade 1, 80.3%; TNM
                                                                                                                           AS according to the following       Grade 2, 19.7%.
                                                                                                                           criteria were selected: stage ≤2
                                                                                                                           and a tumor grade of ≤2 as          Stage: “AS,” stage 1, 67.6%;
                                                                                                                           determined with a biopsy at         stage 2, 32.4%. RT, stage 1,
                                                                                                                           diagnosis. These patients           69%; stage 2, 31%.
                                                                                                                           thereafter received either no
                                                                                                                           active treatment or at most, a
                                                                                                                           TURP after diagnosis were
                                                                                                                           matched with patients who had
                                                                                                                           received EBRT as a primary
                                                                                                                           treatment at diagnosis on (a)
                                                                                                                           cancer stage, (b) tumor grade,
                                                                                                                           (c) age at diagnosis (within 2 yr).




















                                        b  Although the authors referred to this group as “active surveillance” the study did not report following a predefined monitoring protocol; furthermore, patients in
                                        this group “received either no active treatment or at most, a TURP after diagnosis.” For these reasons we did not consider this a comparative study of AS.




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