Noncoding mutations drive persistence of a founder preleukemic clone which initiates late relapse in T-ALL

Blood. 2024 Mar 7;143(10):933-937. doi: 10.1182/blood.2023021906.

Abstract

T-ALL relapse usually occurs early but can occur much later, which has been suggested to represent a de novo leukemia. However, we conclusively demonstrate late relapse can evolve from a pre-leukemic subclone harbouring a non-coding mutation that evades initial chemotherapy.

MeSH terms

  • Chronic Disease
  • Clone Cells
  • Humans
  • Leukemia-Lymphoma, Adult T-Cell*
  • Mutation
  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma* / genetics
  • Recurrence