TY - JOUR
T1 - Molecular-Based Ecosystem to Improve Personalized Medicine in Chronic Myelomonocytic Leukemia
AU - for the iCPSS Alliance
AU - Lanino, Luca
AU - Hunter, Anthony M.
AU - Gagelmann, Nico
AU - Robin, Marie
AU - Dall'Olio, Daniele
AU - Flamigni, Alice
AU - Sala, Claudia
AU - Gurnari, Carmelo
AU - Wang, Yu Hung
AU - Pleyer, Lisa
AU - Xicoy, Blanca
AU - Montalban-Bravo, Guillermo
AU - Shih, Lee Yung
AU - Alsugair, Ali
AU - Fathima, Saubia
AU - Gregorio, Caterina
AU - Rollo, Cesare
AU - Palomo, Laura
AU - Platzbecker, Anne Sophie
AU - Asti, Gianluca
AU - Itzykson, Raphael
AU - Sallman, David A.
AU - Fariselli, Piero
AU - Kern, Wolfgang
AU - Garcia-Manero, Guillermo
AU - Platzbecker, Uwe
AU - Solé, Francesc
AU - Diez-Campelo, Maria
AU - Maciejewski, Jaroslaw
AU - Bejar, Rafael
AU - Thol, Felicitas
AU - Kroger, Nicolaus
AU - Savona, Michael
AU - Fenaux, Pierre
AU - Sanz, Guillermo
AU - Kordasti, Shahram
AU - Santini, Valeria
AU - Fontenay, Michaela
AU - Zeidan, Amer M.
AU - Komrokji, Rami S.
AU - Haferlach, Torsten
AU - Germing, Ulrich
AU - Castellani, Gastone
AU - D'Amico, Saverio
AU - Patnaik, Mrinal
AU - Ieva, Francesca
AU - Solary, Eric
AU - Tefferi, Ayalew
AU - Padron, Eric
AU - Griffiths, Elizabeth
N1 - Publisher Copyright:
© 2026 by American Society of Clinical Oncology
PY - 2026/6/10
Y1 - 2026/6/10
N2 - PURPOSE – Chronic myelomonocytic leukemia (CMML) is a rare myeloid neoplasm characterized by clinical heterogeneity and is associated with poor outcomes. To date, limited molecular information has been incorporated into disease classification and risk stratification. We aimed to integrate genomic features into the clinical decision-making process for CMML.PATIENTS AND METHODS – We analyzed a retrospective cohort of 3013 patients with CMML (training set) and a prospective population of 516 patients (validation set). Using an innovative framework for multimodal data analysis, we developed molecular-based disease taxonomy and prognostication.RESULTS – Unsupervised clustering identified nine entities with distinct genomic features and outcomes (P <.001), including splicing machinery, transcription factors, signal transduction and tyrosine kinase pathways aberrations, and high-risk molecular signatures. Notably, 15% of patients showed molecular/clinical overlap with other myeloid neoplasms. We integrated molecular and clinical information to build the international CMML Prognostic Scoring System (iCPSS), incorporating mutations in nine genes together with hematologic parameters and cytogenetic abnormalities. The iCPSS identified five groups with distinct probability of overall and leukemia-free survival in both training and validation cohorts (P <.001), outperforming existing prognostic models. Importantly, 55% of patients were reassigned to higher or lower risk groups by the iCPSS. Decision analysis demonstrated that iCPSS could refine the optimal timing of allogeneic transplantation at the individual level; compared with conventional prognostic tools, iCPSS-based decision modeling changed transplantation strategy in 31% of cases, resulting in a significant gain-in-life expectancy for eligible patient population (P <.001). A federated learning platform was implemented to enable continuous, privacy-preserving model update across multiple centers.CONCLUSION – Molecular information improves CMML classification and prognostication, supports more effective clinical decision making, and potentially refines the design of clinical trials.
AB - PURPOSE – Chronic myelomonocytic leukemia (CMML) is a rare myeloid neoplasm characterized by clinical heterogeneity and is associated with poor outcomes. To date, limited molecular information has been incorporated into disease classification and risk stratification. We aimed to integrate genomic features into the clinical decision-making process for CMML.PATIENTS AND METHODS – We analyzed a retrospective cohort of 3013 patients with CMML (training set) and a prospective population of 516 patients (validation set). Using an innovative framework for multimodal data analysis, we developed molecular-based disease taxonomy and prognostication.RESULTS – Unsupervised clustering identified nine entities with distinct genomic features and outcomes (P <.001), including splicing machinery, transcription factors, signal transduction and tyrosine kinase pathways aberrations, and high-risk molecular signatures. Notably, 15% of patients showed molecular/clinical overlap with other myeloid neoplasms. We integrated molecular and clinical information to build the international CMML Prognostic Scoring System (iCPSS), incorporating mutations in nine genes together with hematologic parameters and cytogenetic abnormalities. The iCPSS identified five groups with distinct probability of overall and leukemia-free survival in both training and validation cohorts (P <.001), outperforming existing prognostic models. Importantly, 55% of patients were reassigned to higher or lower risk groups by the iCPSS. Decision analysis demonstrated that iCPSS could refine the optimal timing of allogeneic transplantation at the individual level; compared with conventional prognostic tools, iCPSS-based decision modeling changed transplantation strategy in 31% of cases, resulting in a significant gain-in-life expectancy for eligible patient population (P <.001). A federated learning platform was implemented to enable continuous, privacy-preserving model update across multiple centers.CONCLUSION – Molecular information improves CMML classification and prognostication, supports more effective clinical decision making, and potentially refines the design of clinical trials.
UR - https://www.scopus.com/pages/publications/105041629899
U2 - 10.1200/JCO-25-02116
DO - 10.1200/JCO-25-02116
M3 - Article
C2 - 41894646
AN - SCOPUS:105041629899
SN - 0732-183X
VL - 44
SP - 1608
EP - 1623
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 17
ER -