<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wong CH</submitter><funding>Hong Kong Government</funding><pagination>466</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11297067</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Previously, in a randomised trial we demonstrated bipolar transurethral resection of bladder tumor (TURBT) could achieve a higher detrusor sampling rate than monopolar TURBT. We hereby report the long-term oncological outcomes following study intervention.&lt;h4>Methods&lt;/h4>This is a post-hoc analysis of a randomized phase III trial comparing monopolar and bipolar TURBT. Only patients with pathology of non-muscle invasive bladder cancer (NMIBC) were included in the analysis. Per-patient analysis was performed. Primary outcome was recurrence-free survival (RFS). Secondary outcomes included progression-free survival (PFS), cancer-specific survival (CSS) and overall survival (OS).&lt;h4>Results&lt;/h4>From the initial trial, 160 cases were randomised to receive monopolar or bipolar TURBT. 24 cases of non-urothelial carcinoma, 22 cases of muscle-invasive bladder cancer, and 9 cases of recurrences were excluded. A total of 97 patients were included in the analysis, with 46 in the monopolar and 51 in the bipolar group. The median follow-up was 97.1 months. Loss-to-follow-up rate was 7.2%. Regarding the primary outcome of RFS, there was no significant difference (HR = 0.731; 95%CI = 0.433-1.236; P = 0.242) between the two groups. PFS (HR = 1.014; 95%CI = 0.511-2.012; P = 0.969), CSS (HR = 0.718; 95%CI = 0.219-2.352; P = 0.584) and OS (HR = 1.135; 95%CI = 0.564-2.283; P = 0.722) were also similar between the two groups. Multifocal tumours were the only factor that was associated with worse RFS.&lt;h4>Conclusion&lt;/h4>Despite the superiority in detrusor sampling rate, bipolar TURBT was unable to confer long-term oncological benefits over monopolar TURBT.</pubmed_abstract><journal>World journal of urology</journal><pubmed_title>Monopolar versus bipolar transurethral resection of bladder Tumour: post-hoc analysis of a prospective trial.</pubmed_title><pmcid>PMC11297067</pmcid><funding_grant_id>14117421; 14120620</funding_grant_id><pubmed_authors>Yuen SK</pubmed_authors><pubmed_authors>Ng CF</pubmed_authors><pubmed_authors>Wong CH</pubmed_authors><pubmed_authors>Leung DK</pubmed_authors><pubmed_authors>Lim JY</pubmed_authors><pubmed_authors>Ko IC</pubmed_authors><pubmed_authors>Teoh JY</pubmed_authors><pubmed_authors>Yip SY</pubmed_authors><pubmed_authors>Chan ES</pubmed_authors></additional><is_claimable>false</is_claimable><name>Monopolar versus bipolar transurethral resection of bladder Tumour: post-hoc analysis of a prospective trial.</name><description>&lt;h4>Introduction&lt;/h4>Previously, in a randomised trial we demonstrated bipolar transurethral resection of bladder tumor (TURBT) could achieve a higher detrusor sampling rate than monopolar TURBT. We hereby report the long-term oncological outcomes following study intervention.&lt;h4>Methods&lt;/h4>This is a post-hoc analysis of a randomized phase III trial comparing monopolar and bipolar TURBT. Only patients with pathology of non-muscle invasive bladder cancer (NMIBC) were included in the analysis. Per-patient analysis was performed. Primary outcome was recurrence-free survival (RFS). Secondary outcomes included progression-free survival (PFS), cancer-specific survival (CSS) and overall survival (OS).&lt;h4>Results&lt;/h4>From the initial trial, 160 cases were randomised to receive monopolar or bipolar TURBT. 24 cases of non-urothelial carcinoma, 22 cases of muscle-invasive bladder cancer, and 9 cases of recurrences were excluded. A total of 97 patients were included in the analysis, with 46 in the monopolar and 51 in the bipolar group. The median follow-up was 97.1 months. Loss-to-follow-up rate was 7.2%. Regarding the primary outcome of RFS, there was no significant difference (HR = 0.731; 95%CI = 0.433-1.236; P = 0.242) between the two groups. PFS (HR = 1.014; 95%CI = 0.511-2.012; P = 0.969), CSS (HR = 0.718; 95%CI = 0.219-2.352; P = 0.584) and OS (HR = 1.135; 95%CI = 0.564-2.283; P = 0.722) were also similar between the two groups. Multifocal tumours were the only factor that was associated with worse RFS.&lt;h4>Conclusion&lt;/h4>Despite the superiority in detrusor sampling rate, bipolar TURBT was unable to confer long-term oncological benefits over monopolar TURBT.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-04-17T13:05:29.12Z</modification><creation>2025-02-19T02:27:35.283Z</creation></dates><accession>S-EPMC11297067</accession><cross_references><pubmed>39093420</pubmed><doi>10.1007/s00345-024-05124-9</doi></cross_references></HashMap>