A Clinical Prognostic Model Based on Machine Learning from the Fondazione Italiana Linfomi (FIL) MCL0208 Phase III Trial

Multicenter clinical trials are producing growing amounts of clinical data. Machine Learning (ML) might facilitate the discovery of novel tools for prognostication and disease-stratification. Taking advantage of a systematic collection of multiple variables, we developed a model derived from data co...

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Veröffentlicht in:Cancers 2021-12, Vol.14 (1), p.188
Hauptverfasser: Zaccaria, Gian Maria, Ferrero, Simone, Hoster, Eva, Passera, Roberto, Evangelista, Andrea, Genuardi, Elisa, Drandi, Daniela, Ghislieri, Marco, Barbero, Daniela, Del Giudice, Ilaria, Tani, Monica, Moia, Riccardo, Volpetti, Stefano, Cabras, Maria Giuseppina, Di Renzo, Nicola, Merli, Francesco, Vallisa, Daniele, Spina, Michele, Pascarella, Anna, Latte, Giancarlo, Patti, Caterina, Fabbri, Alberto, Guarini, Attilio, Vitolo, Umberto, Hermine, Olivier, Kluin-Nelemans, Hanneke C, Cortelazzo, Sergio, Dreyling, Martin, Ladetto, Marco
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Sprache:eng
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Zusammenfassung:Multicenter clinical trials are producing growing amounts of clinical data. Machine Learning (ML) might facilitate the discovery of novel tools for prognostication and disease-stratification. Taking advantage of a systematic collection of multiple variables, we developed a model derived from data collected on 300 patients with mantle cell lymphoma (MCL) from the Fondazione Italiana Linfomi-MCL0208 phase III trial (NCT02354313). We developed a score with a clustering algorithm applied to clinical variables. The candidate score was correlated to overall survival (OS) and validated in two independent data series from the European MCL Network (NCT00209222, NCT00209209); Results: Three groups of patients were significantly discriminated: Low, Intermediate (Int), and High risk (High). Seven discriminants were identified by a feature reduction approach: albumin, Ki-67, lactate dehydrogenase, lymphocytes, platelets, bone marrow infiltration, and B-symptoms. Accordingly, patients in the Int and High groups had shorter OS rates than those in the Low and Int groups, respectively (Int→Low, HR: 3.1, 95% CI: 1.0-9.6; High→Int, HR: 2.3, 95% CI: 1.5-4.7). Based on the 7 markers, we defined the engineered MCL international prognostic index (eMIPI), which was validated and confirmed in two independent cohorts; Conclusions: We developed and validated a ML-based prognostic model for MCL. Even when currently limited to baseline predictors, our approach has high scalability potential.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers14010188