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March 21, 2026BJU International2 citations

Refining BCG ‐failure classifications in non‐muscle‐invasive bladder cancer

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AŚAleksander ŚlusarczykPSPietro ScilipotiRCRoberto Contieri

Key Points

  • The aim is to validate BCG classification definitions and assess prognostic differences in NMIBC.
  • Utilized a multicentre cohort of 3806 BCG-treated patients.
  • Included 591 patients with high-grade NMIBC recurrence after BCG.
  • Assessed progression-free survival, cancer-specific mortality, and overall mortality as endpoints.
  • Employed cumulative incidence functions, competing-risk models, and multivariable Cox regression for analysis.
  • BCG-unresponsive and BCG-exposed showed similar progression-free survival and mortality rates.
  • 5-year progression rates varied among subgroups, with 29% for BCG-unresponsive and 32.5% for late relapses.
  • Late relapses and BCG-exposed after inadequate BCG demonstrated higher risks of progression.
  • Very late relapses had better prognoses compared to other subgroup classifications.

Abstract

Objective To validate International Bladder Cancer Group (IBCG) definitions of Bacillus Calmette‐Guérin (BCG)‐unresponsive and BCG‐exposed non‐muscle‐invasive bladder cancer (NMIBC) and assess prognostic heterogeneity across various BCG‐failure types. Patients and Methods From a multicentre international cohort of 3806 BCG‐treated patients, 591 who developed high‐grade NMIBC recurrence following BCG between 2003 and 2024 were included. Progression‐free survival (PFS) was the primary endpoint; cancer‐specific (CSM) and overall mortality (OM) were secondary endpoints. Cumulative incidence functions, competing‐risk models and multivariable Cox regression were used. Results Patients with BCG‐unresponsive and BCG‐exposed disease showed similar PFS, CSM, and OM (all P > 0.05). When stratified into five subgroups, prognosis varied: 5‐year progression rates were 29% for BCG‐unresponsive, 32.5% for late relapse (between 6 and 24 months) after adequate BCG, 30% for BCG‐exposed with inadequate BCG (24 months since last BCG) ( P < 0.01). In multivariable analysis, BCG‐exposed after inadequate BCG (subdistribution hazard ratio sHR 3.42, 95% confidence interval CI 1.33–8.84), late relapse (sHR 3.74, 95% CI 1.59–8.78), and BCG‐unresponsive (sHR 2.34, 95% CI 1.00–5.44) were associated with higher progression risks compared to very late relapse. Limitations include retrospective design and treatment heterogeneity. Conclusions Under IBCG definitions, BCG‐unresponsive and BCG‐exposed NMIBC have similarly poor outcomes. A refined classification reveals prognostic heterogeneity, with late relapses after adequate BCG demonstrating outcomes comparable to BCG‐unresponsive, and very late relapses conferring better prognosis.

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Cite This Study

Ślusarczyk et al. (2026) studied this question.

synapsesocial.com/papers/69be37b96e48c4981c677a18https://doi.org/10.1111/bju.70231
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