# Prognostic Factors of Survival in Patients with Surgically Treated Penile Squamous Cell Carcinoma: A Retrospective Cohort Analysis

**Authors:** Andrei Andreșanu, Constantin Gîngu, Dragoș Eugen Georgescu, Mihaela Roxana Oliță, Mihai Adrian Dobra, Cristian Mirvald, Bogdan Obrișcă, Mihai-Adrian Eftimie, Ioanel Sinescu

PMC · DOI: 10.3390/cancers18060952 · 2026-03-14

## TL;DR

This study identifies three factors that predict survival in penile cancer patients, including a newly recognized factor called urethral invasion, which could improve treatment decisions.

## Contribution

The study is the first in Romania to identify urethral invasion as an independent prognostic factor for penile cancer survival.

## Key findings

- Urethral invasion, advanced tumor stage, and extensive lymph node involvement independently predict worse survival in penile cancer patients.
- Patients without urethral invasion had significantly longer median overall survival (63 months vs. 11 months).
- A three-variable prognostic model demonstrated good discrimination (C-index 0.78) for predicting survival outcomes.

## Abstract

Penile cancer is a rare but serious disease. Predicting which patients will have better or worse outcomes after treatment is difficult, especially in eastern Europe, where evidence is limited. We studied 60 patients who underwent surgery for penile cancer at a Romanian tertiary uro-oncology center to identify which factors predict survival. We found that three features independently predicted worse outcomes: advanced tumor stage, extensive lymph node involvement and urethral invasion. Notably, urethral invasion emerged as a newly recognized predictor that is not currently included in standard staging systems. These findings suggest that a three-factor model for predicting survival can be used to counsel patients more accurately, guide treatment intensity and identify individuals at high risk who may benefit from more aggressive therapy.

Background/Objectives: Penile squamous cell carcinoma (PSCC) is a rare malignancy with a potential major impact on survival. Prognostic assessment remains challenging, particularly in underrepresented eastern European populations, where region-specific evidence is lacking. This paper aimed to identify independent predictors of overall survival in surgically treated patients with PSCC from a Romanian high-volume tertiary center. Methods: This retrospective cohort study analyzed 60 patients who were surgically treated for PSCC between October 2020 and December 2024. Univariate and multivariate Cox proportional hazards regression analyses were performed to identify independent prognostic factors. Results: The mean patient age was 62 ± 12 years. T-stage distribution showed 30% pT1, 35% pT2, 31.67% pT3, and 3.33% pT4, with 55% of patients presenting with nodal metastases. Univariate analyses demonstrated significant associations between lymphovascular invasion (p < 0.001), perineural invasion (p = 0.022), and positive surgical margins (p = 0.030) and risk of death. Multivariate analysis identified three independent prognostic factors: absence of histologically documented urethral invasion (HR 0.32; p = 0.027), T3–T4 disease (HR 8.26; p = 0.005 vs. T1), and N3 stage (HR 3.53; p = 0.030 vs. N0–N1). Patients without urethral invasion demonstrated significantly longer median overall survival (63 months vs. 11 months). The final three-variable prognostic model demonstrated good discrimination (C-index 0.78), providing a potential practical risk stratification tool. Conclusions: Urethral invasion, advanced T-stage, and N3 disease independently predict poor survival in surgically treated PSCC. The identification of urethral invasion as an independent prognostic factor warrants consideration in clinical practice. This is the first study of a Romanian cohort to provide critical data for risk-adapted treatment strategies in underrepresented eastern European populations.

## Linked entities

- **Diseases:** penile squamous cell carcinoma (MONDO:0018352), penile cancer (MONDO:0001325)

## Full-text entities

- **Diseases:** malignancy (MESH:D009369), PSCC (MESH:D002294), nodal metastases (MESH:D009362), N3 disease (MESH:D004194), death (MESH:D003643), Urethral (MESH:D014526)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13025001/full.md

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Source: https://tomesphere.com/paper/PMC13025001