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ORIGINAL RESEARCH article

Front. Oncol.

Sec. Surgical Oncology

This article is part of the Research TopicApproaches and Advances in Urologic Cancer EpidemiologyView all 5 articles

Preoperative Inflammation-Based Immune Prognostic Nomogram in Bladder Cancer: A Multicenter Study

Provisionally accepted
  • 1Department of Pathology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China
  • 2Department of Oral and Maxillofacial Surgery, Stomatological Hospital, Kunming Medical University, Kunming, China
  • 3department of Emergency Medicine, Kunming Third People's Hospital, Kunming, China
  • 4Department of Urology, The First Affiliated Hospital of Kunming Medical University, Kunming, China
  • 5Department of Laboratory Medicine, The Second Affiliated Hospital of Kunming Medical University, Kunming, China

The final, formatted version of the article will be published soon.

Background: The systemic inflammatory response has been increasingly recognized as a crucial determinant of tumor progression and prognosis across various malignancies, including bladder cancer (BCa). Preoperative inflammation-based indices, which reflect the dynamic interaction between the tumor and host immune system, offer promising prognostic insights. However, existing studies have largely overlooked the synergistic integration of these indices with histopathological factors into a validated clinical tool for individualized survival prediction following radical cystectomy (RC). Methods: We conducted a retrospective multicenter study involving 1,387 BCa patients who underwent RC at two tertiary hospitals in Yunnan, China, from 2014 to 2024. Key preoperative systemic inflammatory indices—including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), and systemic inflammation response index (SIRI)—were extracted alongside clinical and pathological variables such as AJCC stage, perineural invasion (PNI), and lymphovascular invasion (LVI). Variable selection was performed via LASSO regression, and independent predictors were identified using multivariate Cox regression. A prognostic nomogram was developed and validated through concordance index (C-index), time-dependent ROC curves, calibration plots, and decision curve analysis (DCA). Results: The final nomogram included five independent predictors: NLR, PLR, AJCC stage, PNI, and LVI. The model demonstrated robust discrimination with C-indices of 0.78 in the training cohort and 0.72 in the external validation cohort. AUC values consistently exceeded 0.75 at 1-, 3-, and 5-year timepoints. Calibration plots showed excellent agreement between predicted and observed outcomes, and DCA confirmed meaningful clinical benefit across various threshold probabilities. Conclusion:This study presents a validated, inflammation-based prognostic nomogram that combines preoperative hematologic indices with pathological features to predict overall survival in BCa patients undergoing RC. The model is non-invasive, cost-effective, and easy to implement using routine clinical data. Its strong predictive performance supports its application in preoperative counseling, individualized surveillance strategies, and decision-making regarding adjuvant therapy, contributing to more precise and personalized management in bladder cancer care.

Keywords: Bladder cancer, Radical cystectomy, systemic inflammation, NLR, Prognostic Nomogram, overall survival, immune microenvironment, tumor inflammation

Received: 12 Jun 2025; Accepted: 30 Nov 2025.

Copyright: © 2025 Feng, Zhang, Tao, Jian and Wenlin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Tai Wenlin

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