“Myeloid” Mutations in ALL Are Not Uncommon: Implications for Etiology and Therapies

Author:

Iacobucci Ilaria1ORCID

Affiliation:

1. 1Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Abstract

Summary: In Blood Cancer Discovery, Saygin and colleagues report that somatic variants that are recurrent in myeloid malignancies can also occur with high frequency (16%) in adult acute lymphoblastic leukemia (ALL) where they correlate with older age, diagnosis following genotoxic therapy for a prior malignancy and worse outcome to chemotherapy. Mutations in these “myeloid” genes can precede ALL diagnosis and arise in hematopoietic stem or progenitor cells that clonally expand and differentiate into both lymphoblasts and nonmalignant myeloid cells, supporting a role for clonal hematopoiesis as premalignant state outside the context of myeloid malignancies and providing implications for both ALL etiology and therapeutic intervention. See related article by Saygin et al., p. 164 (4).

Publisher

American Association for Cancer Research (AACR)

Reference10 articles.

1. Causes and consequences of clonal hematopoiesis;Weeks;Blood,2023

2. Distinction of lymphoid and myeloid clonal hematopoiesis;Niroula;Nat Med,2021

3. Therapy-related acute lymphoblastic leukemia is a distinct entity with adverse genetic features and clinical outcomes;Saygin;Blood Adv,2019

4. Acute lymphoblastic leukemia with myeloid mutations is a high-risk disease associated with clonal hematopoiesis;Saygin;Blood Cancer Discov,2024

5. Biologic and therapeutic implications of genomic alterations in acute lymphoblastic leukemia;Iacobucci;J Clin Med,2021

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