Childhood B cell leukemia: Intercepting the paths to progression

Author:

Cobaleda Cesar1,Vicente‐Dueñas Carolina2ORCID,Nichols Kim E.3,Sanchez‐Garcia Isidro45ORCID

Affiliation:

1. Immune System Development and Function Unit Centro de Biología Molecular Severo Ochoa (CBM, CSIC‐UAM) Madrid Spain

2. Institute for Biomedical Research of Salamanca (IBSAL), Department of Pediatrics Hospital Universitario de Salamanca Salamanca Spain

3. Division of Cancer Predisposition St. Jude Children's Research Hospital Memphis Tennessee USA

4. Institute for Biomedical Research of Salamanca (IBSAL) Salamanca Spain

5. Experimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer CSIC/Universidad de Salamanca Salamanca Spain

Abstract

AbstractB‐cell Acute Lymphoblastic Leukemia (B‐ALL) is the most common pediatric cancer, arising most often in children aged 2–5 years. This distinctive age distribution hints at an association between B‐ALL development and disrupted immune system function during a susceptible period during childhood, possibly triggered by early exposure to infection. While cure rates for childhood B‐ALL surpass 90% in high‐income nations, survivors suffer from diminished quality of life due to the side effects of treatment. Consequently, understanding the origins and evolution of B‐ALL, and how to prevent this prevalent childhood cancer, is paramount to alleviate this substantial health burden. This article provides an overview of our current understanding of the etiology of childhood B‐ALL and explores how this knowledge can inform preventive strategies.

Funder

Fundación Ramón Areces

National Cancer Institute

National Institute of Allergy and Infectious Diseases

Histiocytosis Association

Cures Within Reach

Federación Española de Enfermedades Raras

Junta de Castilla y León

Publisher

Wiley

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