Outcomes of Patients with Bacillus Calmette-Guérin (BCG)-Unresponsive Non-Muscle Invasive Bladder Cancer as Defined by the U.S. Food and Drug Administration.

Non-muscle invasive bladder cancer bacillus Calmette-Guérin bladder conserving treatment radical cystectomy

Journal

Bladder cancer (Amsterdam, Netherlands)
ISSN: 2352-3735
Titre abrégé: Bladder Cancer
Pays: Netherlands
ID NLM: 101668567

Informations de publication

Date de publication:
2022
Historique:
received: 20 12 2021
accepted: 31 05 2022
medline: 15 9 2022
pubmed: 15 9 2022
entrez: 12 7 2024
Statut: epublish

Résumé

Limited data are available on the outcomes of patients with non-muscle invasive bladder cancer (NMIBC) unresponsive to intravesical bacillus Calmette-Guérin (BCG), as defined by the United States Food and Drug Administration. To define the outcomes of patients with BCG-unresponsive NMIBC. This was a retrospective, single-institution observational cohort study. Records of patients managed at our institution for BCG-unresponsive NMIBC between 2005 and 2020 were reviewed and clinical outcomes evaluated. The study included 149 patients. Management was with initial radical cystectomy in 60 patients (40%) and initial bladder-sparing therapy (BST) in 89 patients (60%). Overall survival was greater among patients undergoing RC than BST (HR 1.83, 95% CI 1.04-3.22, Among patients who underwent initial BST for BCG-unresponsive NMIBC, rates of treatment failure were very high. Patients who underwent delayed cystectomy after ≥2 lines of BST had elevated rates of extravesical disease. Our observations emphasize the importance of recent and ongoing clinical trials in this clinical space.

Sections du résumé

BACKGROUND BACKGROUND
Limited data are available on the outcomes of patients with non-muscle invasive bladder cancer (NMIBC) unresponsive to intravesical bacillus Calmette-Guérin (BCG), as defined by the United States Food and Drug Administration.
OBJECTIVE OBJECTIVE
To define the outcomes of patients with BCG-unresponsive NMIBC.
METHODS METHODS
This was a retrospective, single-institution observational cohort study. Records of patients managed at our institution for BCG-unresponsive NMIBC between 2005 and 2020 were reviewed and clinical outcomes evaluated.
RESULTS RESULTS
The study included 149 patients. Management was with initial radical cystectomy in 60 patients (40%) and initial bladder-sparing therapy (BST) in 89 patients (60%). Overall survival was greater among patients undergoing RC than BST (HR 1.83, 95% CI 1.04-3.22,
CONCLUSION CONCLUSIONS
Among patients who underwent initial BST for BCG-unresponsive NMIBC, rates of treatment failure were very high. Patients who underwent delayed cystectomy after ≥2 lines of BST had elevated rates of extravesical disease. Our observations emphasize the importance of recent and ongoing clinical trials in this clinical space.

Identifiants

pubmed: 38993682
doi: 10.3233/BLC-211657
pii: BLC211657
pmc: PMC11181681
doi:

Types de publication

Journal Article

Langues

eng

Pagination

303-314

Informations de copyright

© 2022 – The authors. Published by IOS Press.

Déclaration de conflit d'intérêts

Y.L. is an Editorial Board Member of this journal but was not involved in the peer-review process nor had access to any information regarding its peer-review. Y.L. reports relationships with the following entities: Abbott, Abbvie, Ambu, AstraZeneca, BioCanCell, CAPs Medical, Cepheid, Cleveland Diagnostics, C2I Genomics, Fergene, Ferring Research, FKD, GenomeDx Biosciences, Hitachi, Karl Storz, MDxHealth, Merck, Nanorobotics, Nucleix, Pacific Edge, Photocure, Seattle Genetics, Stimit, Verity Pharmaceuticals, Vessi Medical, Virtuoso Surgical. J.M.H., G.S.C., A.T., K.N., V.M. and S.L.W. report no conflicts.

Auteurs

Jeffrey M Howard (JM)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Division of Urology, Maine Medical Center, Portland, ME, USA.

Grayden S Cook (GS)

School of Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Division of Urology, Brigham and Women's Hospital / Harvard Medical School, Boston, MA, USA.

Aaron Tverye (A)

School of Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Department of Urology, University of Kansas Medical Center, Kansas City, KS, USA.

Karabi Nandy (K)

Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Vitaly Margulis (V)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Solomon L Woldu (SL)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Yair Lotan (Y)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Classifications MeSH