Rapid epigenomic classification of acute leukemia

Nat Genet. 2025 Oct;57(10):2456-2467. doi: 10.1038/s41588-025-02321-z. Epub 2025 Sep 22.

Abstract

Acute leukemia requires precise molecular classification and urgent treatment. However, standard-of-care diagnostic tests are time-intensive and do not capture the full spectrum of acute leukemia heterogeneity. Here, we developed a framework to classify acute leukemia using genome-wide DNA methylation profiling. We first assembled a comprehensive reference cohort (n = 2,540 samples) and defined 38 methylation classes. Methylation-based classification matched standard-pathology lineage classification in most cases and revealed heterogeneity in addition to that captured by genetic categories. Using this reference, we developed a neural network (MARLIN; methylation- and AI-guided rapid leukemia subtype inference) for acute leukemia classification from sparse DNA methylation profiles. In retrospective cohorts profiled by nanopore sequencing, high-confidence predictions were concordant with conventional diagnoses in 25 out of 26 cases. Real-time MARLIN classification in patients with suspected acute leukemia provided accurate predictions in five out of five cases, which were typically generated within 2 h of sample receipt. In summary, we present a framework for rapid acute leukemia classification that complements and enhances standard-of-care diagnostics.

MeSH terms

  • Adult
  • DNA Methylation* / genetics
  • Epigenesis, Genetic
  • Epigenomics* / methods
  • Female
  • Humans
  • Leukemia* / classification
  • Leukemia* / diagnosis
  • Leukemia* / genetics
  • Leukemia, Myeloid, Acute* / classification
  • Leukemia, Myeloid, Acute* / genetics
  • Male
  • Neural Networks, Computer
  • Retrospective Studies