After institutional review board approval, our prospectively-maintained clinical database was queried for men who underwent a RP at Memorial Sloan Kettering Cancer Center (MSKCC) between 2006–2012 as the primary treatment for prostate cancer and who had at least one high-risk criteria as defined by the NCCN: PSA 20 ng/mL or higher, clinical stage T3 or greater, or preoperative Gleason score 8–10.14 Patients were excluded if they had undergone previous radiotherapy or ADT.
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