Background: Approximately 70% of bladder cancer is diagnosed as non-muscle invasive (NMIBC) and inflammation is known to impact the oncological outcomes. Adjuvant intravesical BCG in intermediate/high risk can lower recurrence and progression. The efficacy of intravesical BCG can be impacted by smoking effects on systemic inflammation. Methods: Our retrospective, multicenter study with data from 1.313 NMIBC patients aimed to assess the impact of smoking and the systemic inflammatory status on BCG response in T1G3 bladder cancer, using a machine-learning CART based algorithm. Results: In a median of 50-month follow-up (IQR 41-75), 344 patients experienced progression to muscle invasive or metastatic disease and 65 died due to bladder cancer. A CART algorithm has been employed to stratify patients in three prognostic clusters using smoking status, LMR (lymphocytes to monocytes ratio), NLR (neutrophil-to-lymphocyte ratio) and PLR (platelet-to-lymphocyte ratio) as variables. Cox regression models revealed a 1.5-fold (HR 1.66, 95%, CI 1.20-2.29, P=0.002) and three-fold (HR 2.99, 95% CI 2.08-4.30, P<0.001) risk of progression, in intermediate and high risk NMIBC respectively, compared to the low-risk group. The model's concordance index was 0.66. Conclusions: Our study provides an insight into the influence of smoking on inflammatory markers and BCG response in NMIBC patients. Our machine-learning approach provides clinicians a valuable tool for risk stratification, treatment, and decision-making. Future research in larger prospective cohorts is required for validating these findings.

Assessing the influence of smoking on inflammatory markers in bacillus Calmette Guérin response among bladder cancer patients: a novel machine-learning approach / Ferro, Matteo; Tataru, Octavian S.; Fallara, Giuseppe; Fiori, Cristian; Manfredi, Matteo; Claps, Francesco; Hurle, Rodolfo; Buffi, Nicolò M.; Lughezzani, Giovanni; Lazzeri, Massimo; Aveta, Achille; Pandolfo, Savio D.; Barone, Biagio; Crocetto, Felice; Ditonno, Pasquale; Lucarelli, Giuseppe; Lasorsa, Francesco; Carrieri, Giuseppe; Busetto, Gian M.; Falagario, Ugo G.; Del Giudice, Francesco; Maggi, Martina; Cantiello, Francesco; Borghesi, Marco; Terrone, Carlo; Bove, Pierluigi; Antonelli, Alessandro; Veccia, Alessandro; Mari, Andrea; Luzzago, Stefano; Gherasim, Raul; TODEA-MOGA, Ciprian; Minervini, Andrea; Musi, Gennaro; Mistretta, Francesco A.; Bianchi, Roberto; Tozzi, Marco; Soria, Francesco; Gontero, Paolo; Marchioni, Michele; Janello, Letizia M.; Terracciano, Daniela; Russo, Giorgio I.; Schips, Luigi; Perdonà, Sisto; Autorino, Riccardo; Catellani, Michele; Sighinolfi, Chiara; Montanari, Emanuele; Di Stasi, Savino M.; Porpiglia, Francesco; Rocco, Bernardo; De Cobelli, Ottavio; Contieri, Roberto. - In: MINERVA UROLOGY AND NEPHROLOGY. - ISSN 2724-6442. - 77:3(2025), pp. 338-346. [10.23736/s2724-6051.24.05876-2]

Assessing the influence of smoking on inflammatory markers in bacillus Calmette Guérin response among bladder cancer patients: a novel machine-learning approach

FERRO, Matteo
Primo
;
CLAPS, Francesco;
2025-01-01

Abstract

Background: Approximately 70% of bladder cancer is diagnosed as non-muscle invasive (NMIBC) and inflammation is known to impact the oncological outcomes. Adjuvant intravesical BCG in intermediate/high risk can lower recurrence and progression. The efficacy of intravesical BCG can be impacted by smoking effects on systemic inflammation. Methods: Our retrospective, multicenter study with data from 1.313 NMIBC patients aimed to assess the impact of smoking and the systemic inflammatory status on BCG response in T1G3 bladder cancer, using a machine-learning CART based algorithm. Results: In a median of 50-month follow-up (IQR 41-75), 344 patients experienced progression to muscle invasive or metastatic disease and 65 died due to bladder cancer. A CART algorithm has been employed to stratify patients in three prognostic clusters using smoking status, LMR (lymphocytes to monocytes ratio), NLR (neutrophil-to-lymphocyte ratio) and PLR (platelet-to-lymphocyte ratio) as variables. Cox regression models revealed a 1.5-fold (HR 1.66, 95%, CI 1.20-2.29, P=0.002) and three-fold (HR 2.99, 95% CI 2.08-4.30, P<0.001) risk of progression, in intermediate and high risk NMIBC respectively, compared to the low-risk group. The model's concordance index was 0.66. Conclusions: Our study provides an insight into the influence of smoking on inflammatory markers and BCG response in NMIBC patients. Our machine-learning approach provides clinicians a valuable tool for risk stratification, treatment, and decision-making. Future research in larger prospective cohorts is required for validating these findings.
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