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      Oncological outcomes of visibly complete transurethral resection prior to neoadjuvant chemotherapy for bladder cancer

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          ABSTRACT

          Purpose:

          To evaluate the potential oncologic benefit of a visibly complete transurethral resection of a bladder tumor (TURBT) prior to neoadjuvant chemotherapy (NAC) and radical cystectomy (RC).

          Materials and Methods:

          We identified patients who received NAC and RC between 2011-2021. Records were reviewed to assess TURBT completeness. The primary outcome was pathologic downstaging (<ypT2N0), with complete pathologic response (ypT0N0) and survival as secondary endpoints. Logistic regression and Cox proportional hazards models were utilized.

          Results:

          We identified 153 patients, including 116 (76%) with a complete TURBT. Sixty-four (42%) achieved <ypT2N0 and 43 (28%) achieved ypT0N0. When comparing those with and without a complete TURBT, there was no significant difference in the proportion with <ypT2N0 (43% vs 38%, P=0.57) or ypT0N0 (28% vs 27%, P=0.87). After median follow-up of 3.6 years (IQR 1.5-5.1), 86 patients died, 37 died from bladder cancer, and 61 had recurrence. We did not observe a statistically significant association of complete TURBT with cancer-specific or recurrence-free survival (p≥0.20), although the hazard of death from any cause was significantly higher among those with incomplete TURBT even after adjusting for ECOG and pathologic T stage, HR 1.77 (95% CI 1.04-3.00, P=.034).

          Conclusions:

          A visibly complete TURBT was not associated with pathologic downstaging, cancer-specific or recurrence-free survival following NAC and RC. These data do not support the need for repeat TURBT to achieve a visibly complete resection if NAC and RC are planned.

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          Most cited references25

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          Diagnosis and Treatment of Non-Muscle Invasive Bladder Cancer: AUA/SUO Guideline.

          Although associated with an overall favorable survival rate, the heterogeneity of non-muscle invasive bladder cancer (NMIBC) affects patients' rates of recurrence and progression. Risk stratification should influence evaluation, treatment and surveillance. This guideline attempts to provide a clinical framework for the management of NMIBC.
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            Neoadjuvant chemotherapy plus cystectomy compared with cystectomy alone for locally advanced bladder cancer.

            Despite aggressive local therapy, patients with locally advanced bladder cancer are at significant risk for metastases. We evaluated the ability of neoadjuvant chemotherapy to improve the outcome in patients with locally advanced bladder cancer who were treated with radical cystectomy. Patients were enrolled if they had muscle-invasive bladder cancer (stage T2 to T4a) and were to be treated with radical cystectomy. They were stratified according to age (less than 65 years vs. 65 years or older) and stage (superficial muscle invasion vs. more extensive disease) and were randomly assigned to radical cystectomy alone or three cycles of methotrexate, vinblastine, doxorubicin, and cisplatin followed by radical cystectomy. We enrolled 317 patients over an 11-year period, 10 of whom were found to be ineligible; thus, 154 were assigned to receive surgery alone and 153 to receive combination therapy. According to an intention-to-treat analysis, the median survival among patients assigned to surgery alone was 46 months, as compared with 77 months among patients assigned to combination therapy (P=0.06 by a two-sided stratified log-rank test). In both groups, improved survival was associated with the absence of residual cancer in the cystectomy specimen. Significantly more patients in the combination-therapy group had no residual disease than patients in the cystectomy group (38 percent vs. 15 percent, P<0.001). As compared with radical cystectomy alone, the use of neoadjuvant methotrexate, vinblastine, doxorubicin, and cisplatin followed by radical cystectomy increases the likelihood of eliminating residual cancer in the cystectomy specimen and is associated with improved survival among patients with locally advanced bladder cancer. Copyright 2003 Massachusetts Medical Society
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              Bladder Cancer, Version 3.2020, NCCN Clinical Practice Guidelines in Oncology

              This selection from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Bladder Cancer focuses on the clinical presentation and workup of suspected bladder cancer, treatment of non–muscle-invasive urothelial bladder cancer, and treatment of metastatic urothelial bladder cancer because important updates have recently been made to these sections. Some important updates include recommendations for optimal treatment of non–muscle-invasive bladder cancer in the event of a bacillus Calmette-Guérin (BCG) shortage and details about biomarker testing for advanced or metastatic disease. The systemic therapy recommendations for second-line or subsequent therapies have also been revised. Treatment and management of muscle-invasive, nonmetastatic disease is covered in the complete version of the NCCN Guidelines for Bladder Cancer available at NCCN.org . Additional topics covered in the complete version include treatment of nonurothelial histologies and recommendations for nonbladder urinary tract cancers such as upper tract urothelial carcinoma, urothelial carcinoma of the prostate, and primary carcinoma of the urethra.
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                Author and article information

                Journal
                Int Braz J Urol
                Int Braz J Urol
                ibju
                International Brazilian Journal of Urology : Official Journal of the Brazilian Society of Urology
                Sociedade Brasileira de Urologia
                1677-5538
                1677-6119
                20 May 2023
                Jul-Aug 2023
                : 49
                : 4
                : 479-489
                Affiliations
                [1 ] orgnameMayo Clinic orgdiv1Department of Urology Jacksonville FL USA originalDepartment of Urology Mayo Clinic, Jacksonville, FL, USA
                [2 ] orgnameTulane University orgdiv1School of Medicine New Orleans LA USA originalTulane University School of Medicine, New Orleans, LA, USA
                [3 ] orgnameUniversity of Alabama orgdiv1Department of Pathology Birmingham AL USA originalDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA
                [4 ] orgnameMayo Clinic orgdiv1Department of Quantitative Health Sciences Jacksonville FL USA originalDepartment of Quantitative Health Sciences, Mayo Clinic, Jacksonville, FL, USA
                Author notes
                Correspondence address: Timothy D. Lyon, MD, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA Fax: +1 904 953-2218 E-mail: lyon.timothy@ 123456mayo.edu

                CONFLICT OF INTEREST

                TDL has served as a consultant for Bristol Myers Squibb and ImmunityBio. All other authors have no conflicts of interest to report.

                Author information
                https://orcid.org/0000-0001-9251-3687
                Article
                S1677-5538.IBJU.2023.0123
                10.1590/S1677-5538.IBJU.2023.0123
                10482438
                37267613
                7f55e5a8-2741-4a20-947f-6fea75bcd47f

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 March 2023
                : 24 April 2023
                Page count
                Figures: 1, Tables: 4, Equations: 0, References: 22, Pages: 11
                Categories
                Original Article

                cystectomy,neoadjuvant therapy,transurethral resection of bladder

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