2015
DOI: 10.1016/j.urolonc.2015.04.004
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Heterogeneity in D׳Amico classification–based low-risk prostate cancer: Differences in upgrading and upstaging according to active surveillance eligibility

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Cited by 41 publications
(41 citation statements)
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“…In selected cohorts of patients under active surveillance, further risk factors associating with disease reclassification have been identified and include cancer involvement >50% per core, the number of biopsy cores and even immediate repeat biopsy [20,21,22]. …”
Section: Discussionmentioning
confidence: 99%
“…In selected cohorts of patients under active surveillance, further risk factors associating with disease reclassification have been identified and include cancer involvement >50% per core, the number of biopsy cores and even immediate repeat biopsy [20,21,22]. …”
Section: Discussionmentioning
confidence: 99%
“…However, low-risk PCA is a heterogeneous population and prostate biopsies can underestimate the true grade of the cancer when compared to prostatectomy specimens as it has been reported in past series referring to the preceding Gleason score system [13,16,17,18]. Recently, in large contemporary series referring to the modified Gleason score system, it has been shown that there is still a wide variation of tumor upgrading, which ranges between 43% [19] and 63.8% [20]. In our study, low-risk PCA, which included 38.8% of the operated cases, tumor upgrade was detected in 65.3% of the surgical specimens.…”
Section: Discussionmentioning
confidence: 99%
“…In contemporary series, it has been shown that independent predictors of tumor upgrading in low-risk PCA include non-white race [19], older age [19,20], higher PSA levels [19,20], higher proportion of positive cores and tumor involvement greater than 50% per each core as well [20]. In our study, we tried to identify prognostic factors associating with tumor upgrading to the pGP = 3 + 4 and to the pGP >3 + 4.…”
Section: Discussionmentioning
confidence: 99%
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“…Second, due to a lack of detailed information from SEER-Medicare-derived analyses, we relied on pathological Gleason score. Since high rates of upgrading were recorded between clinical and pathological Gleason score, 15 a corresponding bias might exist in our analyses. Finally, other limitations known to affect SEER-Medicare-derived analyses are also operational, for example, use of claims data or lack of detailed parameters that are included in prospective trials.…”
Section: Discussionmentioning
confidence: 99%