Cancers (Dec 2021)

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

  • Gian Maria Zaccaria,
  • Simone Ferrero,
  • Eva Hoster,
  • Roberto Passera,
  • Andrea Evangelista,
  • Elisa Genuardi,
  • Daniela Drandi,
  • Marco Ghislieri,
  • Daniela Barbero,
  • Ilaria Del Giudice,
  • Monica Tani,
  • Riccardo Moia,
  • Stefano Volpetti,
  • Maria Giuseppina Cabras,
  • Nicola Di Renzo,
  • Francesco Merli,
  • Daniele Vallisa,
  • Michele Spina,
  • Anna Pascarella,
  • Giancarlo Latte,
  • Caterina Patti,
  • Alberto Fabbri,
  • Attilio Guarini,
  • Umberto Vitolo,
  • Olivier Hermine,
  • Hanneke C Kluin-Nelemans,
  • Sergio Cortelazzo,
  • Martin Dreyling,
  • Marco Ladetto

DOI
https://doi.org/10.3390/cancers14010188
Journal volume & issue
Vol. 14, no. 1
p. 188

Abstract

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Background: 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). Methods: 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.

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