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Molecular-Based Ecosystem to Improve Personalized Medicine in Chronic Myelomonocytic Leukemia

  • for the iCPSS Alliance
  • Yale University
  • Emory University
  • University of Hamburg
  • Université Paris Cité
  • University of Bologna
  • Pancreas Unit, Department of Digestive Diseases and Internal Medicine, SantOrsola-Malpighi Hospital
  • Polytechnic University of Milan
  • Cleveland Clinic Foundation
  • University of Rome Tor Vergata
  • National Taiwan University
  • Paracelsus Private Medical University
  • Autonomous University of Barcelona
  • University of Texas MD Anderson Cancer Center
  • Chang Gung University
  • Mayo Clinic Rochester, MN
  • Karolinska Institutet
  • University of Turin
  • Technische Universität Dresden
  • IRCCS Istituto Clinico Humanitas - Rozzano (Milano)
  • Moffitt Cancer Center
  • Munich Leukemia Laboratory
  • Hospital Clínico Universitario de Salamanca
  • University of California at San Diego
  • Hannover Medical School
  • Vanderbilt University
  • Hospital Universitario La Fe
  • Guy's and St Thomas' NHS Foundation Trust
  • Marche Polytechnic University
  • University of Florence
  • Institut de la Leucémie Paris Saint-Louis
  • Heinrich Heine University Düsseldorf
  • Human Technopole
  • Institut Gustave Roussy

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)1608-1623
Number of pages16
JournalJournal of Clinical Oncology
Volume44
Issue number17
DOIs
StatePublished - Jun 10 2026

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