Metastatic renal cell carcinoma remains clinically challenging because of heterogeneous outcomes and limited predictive biomarkers for immunotherapy. We performed an explainable machine learning analysis using data from the multicenter retrospective Meet-URO 15 study, including 571 patients with metastatic renal cell carcinoma treated with second-line or later nivolumab. Clinical and inflammatory variables were used to develop classification models for disease control rate, progression-free survival at 3 and 9 months, and overall survival at 6, 18 and 24 months, as well as survival models for continuous progression-free and overall survival. Model performance was assessed using weighted F1-score for classification and concordance index for survival analysis, with interpretability provided through Shapley additive explanations. The best classification performance was observed for 6-month overall survival using a support vector machine model combined with minimum redundancy maximum relevance feature selection, achieving an F1-score of 0.81 on the test set and 0.77 in external validation. In survival analysis, random survival forest achieved a test-set concordance index of 0.68 for overall survival. Inflammatory indices, IMDC score, hemoglobin, lymphocytes and platelets consistently emerged as relevant prognostic features. These findings support explainable machine learning as a transparent approach to refine outcome prediction in immunotherapy-treated metastatic renal cell carcinoma.

Explainable machine learning to predict immunotherapy outcomes in metastatic renal cell carcinoma - Meet-URO 15-AI study / Rebuzzi, S.E., Miskovic, V., Fornarini, G., Ferri, S., Buti, S., Piceni, M., Signori, A., Provenzano, L., Banna, G.L., Rescigno, P., Maruzzo, M., Bimbatti, D., Pollone, B.R., Basso, U., De Giorgi, U., Pedrazzoli, P., Galli, L., Zucali, P.A., Di Costanzo, F., Ghose, A., et al.. - In: NPJ PRECISION ONCOLOGY. - ISSN 2397-768X. - 10:1(2026). [10.1038/s41698-026-01576-x]

Explainable machine learning to predict immunotherapy outcomes in metastatic renal cell carcinoma - Meet-URO 15-AI study

Buti, Sebastiano
Investigation
;
2026-01-01

Abstract

Metastatic renal cell carcinoma remains clinically challenging because of heterogeneous outcomes and limited predictive biomarkers for immunotherapy. We performed an explainable machine learning analysis using data from the multicenter retrospective Meet-URO 15 study, including 571 patients with metastatic renal cell carcinoma treated with second-line or later nivolumab. Clinical and inflammatory variables were used to develop classification models for disease control rate, progression-free survival at 3 and 9 months, and overall survival at 6, 18 and 24 months, as well as survival models for continuous progression-free and overall survival. Model performance was assessed using weighted F1-score for classification and concordance index for survival analysis, with interpretability provided through Shapley additive explanations. The best classification performance was observed for 6-month overall survival using a support vector machine model combined with minimum redundancy maximum relevance feature selection, achieving an F1-score of 0.81 on the test set and 0.77 in external validation. In survival analysis, random survival forest achieved a test-set concordance index of 0.68 for overall survival. Inflammatory indices, IMDC score, hemoglobin, lymphocytes and platelets consistently emerged as relevant prognostic features. These findings support explainable machine learning as a transparent approach to refine outcome prediction in immunotherapy-treated metastatic renal cell carcinoma.
2026
Explainable machine learning to predict immunotherapy outcomes in metastatic renal cell carcinoma - Meet-URO 15-AI study / Rebuzzi, S.E., Miskovic, V., Fornarini, G., Ferri, S., Buti, S., Piceni, M., Signori, A., Provenzano, L., Banna, G.L., Rescigno, P., Maruzzo, M., Bimbatti, D., Pollone, B.R., Basso, U., De Giorgi, U., Pedrazzoli, P., Galli, L., Zucali, P.A., Di Costanzo, F., Ghose, A., et al.. - In: NPJ PRECISION ONCOLOGY. - ISSN 2397-768X. - 10:1(2026). [10.1038/s41698-026-01576-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/3078574
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