# Evaluating the Therapeutic Role of Lymph Node Dissection in Variant Subtype Bladder Cancer

**Authors:** Syed Nahiyaan Rahman, Darryl T. Martin, Kandala Keervani, Spencer James, Peter Humphrey, David Hesse, Wei Shen Tan, Sunil Patel, Jonathan Wright, Fady Ghali

PMC · DOI: 10.3390/cancers17152536 · Cancers · 2025-07-31

## TL;DR

This study examines how lymph node dissection affects survival in different types of variant bladder cancer, finding it most beneficial for squamous and adenocarcinoma subtypes.

## Contribution

The study identifies subtype-specific survival benefits of lymph node dissection in variant bladder cancer, highlighting the need for tailored surgical approaches.

## Key findings

- Lymph node dissection significantly improves survival in squamous and adenocarcinoma variant bladder cancer subtypes.
- The benefit of lymph node dissection varies across variant subtypes, with some showing no significant survival improvement.
- Higher pNx rates are observed in certain subtypes, indicating incomplete nodal staging in many cases.

## Abstract

The impact of lymph node dissection at the time of radical cystectomy for urothelial carcinoma has not been well established in the context of variant histologies. The aim of our study was to characterize the impact of node dissection on overall survival across various variant subtypes. We report significant heterogeneity in the use and benefit of LND, with squamous and adenocarcinoma subtypes showing the clearest survival benefit. These findings highlight the importance of a more risk-adapted surgical approach in VBC and the need for further investigation of subtype-specific therapeutic strategies.

Background: The importance of lymph node dissection (LND) at the time of radical cystectomy for urothelial carcinoma (UC) is widely accepted despite known risks. The therapeutic benefits of LND for variant subtype bladder cancer (VBC), a heterogenous and distinct set of diseases, are not well established. We aim to characterize the impact of LND on overall survival across VBC subtypes. Methods: The National Cancer Database was queried for all cases of variant subtype bladder cancer managed with radical cystectomy between 2004 and 2020, using the International Classification of Disease-O-3 morphological codes. The cases were stratified by receipt of individual variant subtypes. The primary outcome was overall survival associated with pathologic nodal status and receipt of nodal dissection. A Kaplan–Meier analysis and Cox proportional hazards analysis were used for survival analyses. Results: A total of 30,911 patients with VBC that were managed with radical cystectomy were included in our analysis. The pNx rates ranged from 33.1% in the micropapillary subtype, 42.2% in the sarcomatoid subtype, 68.4% in the squamous subtype, 48.9% in the adenocarcinoma subtype, and 56.2% in the neuroendocrine subtype. The median OS was higher in those that received a nodal dissection across subtypes but was statistically significant only for the squamous (71.0 [68.0 vs. 74.0] vs. 37.2 [33.6 vs. 40.9] months p < 0.001) and adenocarcinoma (45.9 [32.9 vs. 59.0] vs. 37.9 [28.6 vs. 47.1] months p = 0.037) subtypes. Using Cox proportional hazards regression, LN dissection was associated with improved OS for the squamous (0.50 (0.44–0.58) p < 0.001) and adenocarcinoma (0.65 [0.45–0.93) p = 0.030) subtypes. Conclusions: The role of LND across VBC subtypes is not clearly defined and warrants further investigation to develop a more risk-adaptive approach. We demonstrate heterogeneity with respect to the OS benefit associated with LND at the time of surgery. Among certain VBC subtypes, LND may not offer a significant therapeutic benefit, while LND in squamous and adenocarcinoma VBCs is correlated with improved survival.

## Linked entities

- **Diseases:** urothelial carcinoma (MONDO:0040679)

## Full-text entities

- **Genes:** NODAL (nodal growth differentiation factor) [NCBI Gene 4838] {aka HTX5}
- **Diseases:** UC (MESH:D014523), adenocarcinoma (MESH:D000230), LND (MESH:D000072717), Cancer (MESH:D009369), Bladder Cancer (MESH:D001749), squamous and adenocarcinoma (MESH:D002294)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12346734/full.md

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Source: https://tomesphere.com/paper/PMC12346734