Evidence map›Paper›PMID 42393181›Full record

ArticleNPJ precision oncology2026

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

Sara Elena Rebuzzi, Vanja Miskovic, Giuseppe Fornarini, Sara Ferri, Sebastiano Buti, Matteo Piceni, Alessio Signori, Leonardo Provenzano, Giuseppe Luigi Banna, Pasquale Rescigno and 12 more

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Article in NPJ precision oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Sara Elena Rebuzzi *Medical Oncology Unit, Ospedale San Paolo, Savona, Italy.
Vanja Miskovic *Department of Electronics, Information and Bioengineering, Polytechnic University of Milan, Milan, Italy.
Giuseppe FornariniMedical Oncology Unit, IRCCS Azienda Ospedaliera Metropolitana (IRCCS AOM), IRCCS Ospedale Policlinico San Martino, Genova, Italy. giuseppe.fornarini@aomliguria.it.
Sara FerriDepartment of Electronics, Information and Bioengineering, Polytechnic University of Milan, Milan, Italy.
Sebastiano ButiMedical Oncology Unit, University Hospital of Parma, Parma, Italy.
Matteo PiceniDepartment of Electronics, Information and Bioengineering, Polytechnic University of Milan, Milan, Italy.
Alessio SignoriDepartment of Health Sciences (DISSAL), Section of Biostatistics, University of Genova, Genova, Italy.
Leonardo ProvenzanoDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori (INT), Milan, Italy.
Giuseppe Luigi BannaDepartment of Oncology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK.
Pasquale RescignoTranslational and Clinical Research Institute, Centre for Cancer, Newcastle University, Newcastle Upon Tyne, UK.
Marco MaruzzoOncology Unit 3, Istituto Oncologico Veneto-IOV-IRCCS, Padua, Italy.
Davide BimbattiOncology Unit 1, Istituto Oncologico Veneto-IOV-IRCCS, Padua, Italy.
Beatrice Ramella PolloneMedical Oncology Unit, IRCCS Azienda Ospedaliera Metropolitana (IRCCS AOM), IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Umberto BassoOncology Unit 1, Istituto Oncologico Veneto-IOV-IRCCS, Padua, Italy.
Ugo De GiorgiDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Paolo PedrazzoliMedical Oncology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Luca GalliMedical Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.
Paolo Andrea ZucaliDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Fabrizio Di CostanzoTranslational and Clinical Research Institute, Centre for Cancer, Newcastle University, Newcastle Upon Tyne, UK.
Aruni GhoseBarts Cancer Centre, St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Alessandra Laura Giulia PedrocchiDepartment of Electronics, Information and Bioengineering, Polytechnic University of Milan, Milan, Italy.
Arsela PrelajDepartment of Electronics, Information and Bioengineering, Polytechnic University of Milan, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.