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dc.contributor.authorEl-Taji, Omar
dc.contributor.authorSukumar, S
dc.contributor.authorPiedad, J
dc.contributor.authorGhose, A
dc.contributor.authorHughes, R
dc.contributor.authorOstler, Pete
dc.contributor.authorSharma, A.
dc.contributor.authorLane, T
dc.contributor.authorAdshead, James
dc.contributor.authorVasdev, Nikhil
dc.date.accessioned2023-09-05T16:00:03Z
dc.date.available2023-09-05T16:00:03Z
dc.date.issued2022-12-31
dc.identifier.citationEl-Taji , O , Sukumar , S , Piedad , J , Ghose , A , Hughes , R , Ostler , P , Sharma , A , Lane , T , Adshead , J & Vasdev , N 2022 , ' Single tertiary cancer centre experience on the management of pT3b Prostate Cancer After Robot - assisted Laparoscopic Prostatectomy ' , Current Urology , vol. 16 , no. 4 , pp. 227-231 . https://doi.org/10.1097/CU9.0000000000000115
dc.identifier.issn1661-7649
dc.identifier.urihttp://hdl.handle.net/2299/26630
dc.description© 2022 The Authors. Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.description.abstractBackground Pathological involvement of the seminal vesicle poses a treatment dilemma following robotic prostatectomy. Margin status plays an important role in deciding further management. A wide range of treatment options are available, including active monitoring, adjuvant radiotherapy, salvage radiotherapy, and occasionally androgen deprivation therapy. Patients undergoing postoperative radiotherapy tend to have higher risk of urinary and bowel morbidities. The recent RADICALS-RT concluded that adjuvant radiotherapy did not have any benefit compared with salvage radiotherapy. We aim to audit the incidence, margin status, and management of T3b cancer cases at our center. Materials and methods A retrospective analysis was conducted of all patients diagnosed with pathological T3b (pT3b) prostate cancer following robotic-assisted laparoscopic prostatectomy from January 2012 to July 2020. Preoperative parameters analyzed included prostate-specific antigen (PSA), T stage, and age. A chi-square test and 2-tailed t test were used to determine the relationship between categorical and continuous variables, respectively. Kaplan-Meier survival curves were generated to assess overall survival in patients with pT3b prostate cancer and used to compare unadjusted progression-free survival among those who underwent adjuvant and salvage radiotherapy. Results A total of 83 (5%) of 1665 patients who underwent robotic prostatectomy were diagnosed with pT3b prostate cancer between January 2012 and July 2020. Among these, 36 patients (44%) did not receive any radiotherapy during follow-up, compared with 26 patients (31%) who received adjuvant radiotherapy and 21 (25%) who received salvage radiotherapy. The median age of our cohort was 64 (SD, 6.4) years. Mean PSA at presentation was 12.7 μg/L. Positive margins were seen in 36 patients (43%); however, there was no statistically significant difference between treatment groups (p = 0.49). The median overall survival was 96%. There was no significant difference between the adjuvant and salvage groups in terms of biochemical progression-free survival (p = 0.66). Five-year biochemical progression-free survival was 94% for those in the adjuvant radiotherapy group and 97% for those in the salvage radiotherapy group. Conclusions Our audit corroborates with the recently concluded RADICALS-RT study, although we had fewer patients with positive margins. Radiotherapy can be avoided in patients with T3b prostate cancer, even if margin is positive, until there is definitive evidence of PSA recurrence. In keeping with the conclusion of RADICALS-RT, salvage radiotherapy may be preferable to adjuvant radiotherapy.en
dc.format.extent290695
dc.language.isoeng
dc.relation.ispartofCurrent Urology
dc.titleSingle tertiary cancer centre experience on the management of pT3b Prostate Cancer After Robot - assisted Laparoscopic Prostatectomyen
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionBasic and Clinical Science Unit
dc.contributor.institutionExtracellular Vesicle Research Unit
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1097/CU9.0000000000000115
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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