ArticleWorld journal of urology2026
Development and external validation of a nomogram predicting cancer-specific mortality-free survival after trimodal therapy in muscle-invasive bladder cancer.
Article in World journal of urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.
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
1 citing paper in PubMed.
- Extent of Pelvic Lymph Node Dissection at Partial Cystectomy: Effect on Cancer-Specific Mortality.International journal of urology : official journal of the Japanese Urological Association · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
21 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionWe developed and externally validated a novel population-based model for predicting cancer-specific mortality free survival (CSM-FS) in trimodal therapy (TMT)-treated muscle-invasive bladder cancer (MIBC) patients, and we compared its performance to that of AJCC categories.
methodsWithin the SEER database (2004-2021), we identified MIΒC patients treated with TMT (n = 1801). The population was randomly divided into development (n = 900, 50%) and external validation (n = 901, 50%) cohorts. Univariable Cox-regression models addressing CSM were fitted. Subsequently, the most parsimonious model with the best validation metrics was selected. Accuracy, calibration, and decision curve analyses (DCAs) tested the novel nomogram relative to the AJCC staging within the external validation cohort.
resultsAge at diagnosis, sex, median household income, T stage, N stage, and tumor size qualified for inclusion in the nomogram predicting CSM-FS. In external validation cohort, the accuracy of the novel nomogram predictions at two vs. three vs. four years after TMT was 0.70 vs. 0.67 vs. 0.66, respectively. Conversely, AJCC staging accuracy was 0.57 vs. 0.56 vs. 0.55 for the same timepoints. The novel nomogram predictions were well calibrated relative to observed CSM-FS rates. Finally, in DCAs the novel nomogram outperformed AJCC staging at all three timepoints.
conclusionThe novel nomogram for TMT-treated patients outperformed AJCC-based predictions of CSM-FS, when accuracy and DCAs represented the benchmarks of interest. However, its predictive accuracy is not ideal.
Indexed as
Identifiers
41553578What 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.