ReviewThe Journal of urology2026
Combination Strategies to Enhance Bacillus Calmette-Guérin Efficacy for Nonmuscle-Invasive Bladder Cancer.
Review in The Journal of urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
- Commented on by
- Commented on by
Authors and funding
8 authors.
Funding
Abstract
purposeBacillus Calmette-Guérin (BCG) is the standard of care therapy for high-risk nonmuscle-invasive bladder cancer (NMIBC). However, up to half of patients will experience treatment failure, and many face considerable adverse effects, which can lead to dose reduction and intolerance. Novel bladder-sparing approaches with favorable risk-to-benefit ratio are thus critical in NMIBC. MATERIALS AND
methodsA narrative review of the literature was performed of English-language MEDLINE indexed articles and abstracts of resistance mechanisms to BCG and combination-based strategies to enhance the efficacy of BCG intravesical therapy in high-risk NMIBC.
resultsTreatment options for high-risk NMIBC have expanded considerably over the last few years. Combination strategies represent an opportunity to enhance the effectiveness of BCG and promote durable response. Combination therapies that aim to reduce immunosuppressive cellular populations (regulatory T cells, myeloid-derived suppressor cells) and immune checkpoint blockade offer mechanisms to overcome resistance to BCG therapy. Chemoimmunotherapy and immunotherapy-based combinations represent a bladder preservation strategy that needs to be weighed against oncological efficacy, toxicity, and cost-effectiveness.
conclusionsBCG-based combination therapies have emerged as a strategy to overcome BCG resistance and promote durable responses. Despite their promise, combination design is endless, and adoption remains challenging due to overlapping mechanisms of resistance, adverse events associated with systemic therapy and/or additional intravesical therapy, and financial burden. Long-term multiarm trials are needed for direct comparative analyses between combinations of agents to inform oncological efficacy, safety profile, and cost-effectiveness.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.