2014
DOI: 10.1016/j.urolonc.2012.11.021
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The presence of positive surgical margins in patients with organ-confined prostate cancer results in biochemical recurrence at a similar rate to that in patients with extracapsular extension and PSA≤10ng/ml

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Cited by 9 publications
(14 citation statements)
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“…Most previous studies found that a PSM was a prognostic parameter for postoperative BCR or disease progression of PCa [5,10-12,14,15,17,19]. In contrast with the above studies, several other studies demonstrated that a PSM was not associated with BCR or disease progression [20,21].…”
Section: Discussionmentioning
confidence: 95%
“…Most previous studies found that a PSM was a prognostic parameter for postoperative BCR or disease progression of PCa [5,10-12,14,15,17,19]. In contrast with the above studies, several other studies demonstrated that a PSM was not associated with BCR or disease progression [20,21].…”
Section: Discussionmentioning
confidence: 95%
“…Eminaga et al [27] also investigated the BCR in patients with organ-confined prostate cancer and PSM in a RP series from 1999 to 2008. They divided the patients into 5 groups according to pathological category, PSM, and PSA level: pT2 category without PSM, pT2þ category, pT3a category and PSA r 10 ng/ml, pT3a category and PSA 4 10 ng/ml, and pT3b category.…”
Section: Discussionmentioning
confidence: 99%
“…While many studies have examined pathological features and the risk of BCR [9][10][11][12][13][14][15][16][17], to our knowledge, only two studies [18,19] have directly compared combinations of pathological features as risk factors for BCR and survival outcomes among men with pathological Gleason score 8-10 disease at the time of RP. That said, these studies are >10 years old, and did not examine a heterogeneous cohort of men, whereas in the present study cohort, selected from the SEARCH database, 30% of the men were black.…”
Section: Discussionmentioning
confidence: 99%
“…Not all men with Gleason score 8-10 disease, however, are destined to experience BCR. When assessing risk of recurrence after RP, many studies consider pathological features, either individually, as pathological stage, or in various 'favourable' or 'unfavourable' groupings, as risk factors for BCR or other endpoints, such as prostate cancerspecific survival [5,[8][9][10][11][12][13][14][15][16][17], but while previous studies have examined the relationship between pathological features and BCR in pathological high grade disease [18,19], these studies are >10 years old and, to our knowledge, have not been updated to examine a more racially heterogeneous cohort of men. We therefore used the SEARCH database of men treated with RP [20] to identify men with pathological high grade disease (Gleason score [8][9][10] and to create groups based on various combinations of pathological features and compare these groups with regard to BCR risk.…”
Section: Introductionmentioning
confidence: 99%