# Targeted therapies in pediatric B-Cell acute lymphoblastic leukemia: mechanisms, efficacy, and future directions

**Authors:** Valeria Correa-Carranza, Guillermo Rosario-Méndez, Manuel Castillejos-López, Juan Luis Chávez-Pacheco, Cesar Galván-Díaz, Luz María Torres-Espíndola

PMC · DOI: 10.3389/fphar.2026.1654783 · 2026-01-28

## TL;DR

This review explores how targeted therapies are improving treatment for pediatric B-cell acute lymphoblastic leukemia, offering better outcomes with fewer side effects.

## Contribution

The paper provides a comprehensive analysis of targeted therapies for pediatric B-cell ALL, highlighting their mechanisms and clinical efficacy.

## Key findings

- Targeted therapies improved progression-free survival and overall response rates in relapsed/refractory ALL patients.
- CD19-directed CAR-T-cell therapy and bispecific antibodies like blinatumomab showed high remission rates in early trials.
- BCR-ABL1-positive ALL patients benefited from tyrosine kinase inhibitors combined with chemotherapy.

## Abstract

Acute lymphoblastic leukemia (ALL) is the most common hematologic malignancy in children and is characterized by rapid progression and, in some cases, a high risk of relapse. Targeted therapies have revolutionized treatment with greater specificity, reduced systemic toxicity and a better prognosis.

This review provides a comprehensive analysis of current targeted therapies for pediatric B-cell ALL, focusing on their mechanisms of action, efficacy, safety profiles, advantages, and remaining challenges.

A systematic review of clinical trials published over the past 15 years was conducted. The analyzed therapies include monoclonal antibodies, antibody‒drug conjugates, tyrosine kinase inhibitors, proteasome inhibitors, and chimeric antigen–receptor T-cell (CAR-T cell) immunotherapy.

Targeted therapies improved progression-free survival and overall response rates, particularly in patients with relapsed/refractory ALL. CD19-directed CAR-T-cell therapy and bispecific antibodies (e.g., blinatumomab) have demonstrated high remission rates in early-phase clinical trials. Additionally, BCR-ABL1-positive ALL patients show benefit from tyrosine kinase inhibitors when combined with chemotherapy.

Targeted therapies represent a paradigm shift in ALL treatments, enabling more personalized and effective strategies. Their integration into standard protocols, especially for high-risk and relapsed patients, is crucial to enhancing long-term outcomes.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251110522, identifier CRD420251110522

## Linked entities

- **Proteins:** CD19 (CD19 molecule)
- **Diseases:** acute lymphoblastic leukemia (MONDO:0004967), B-cell acute lymphoblastic leukemia (MONDO:0004947)

## Full-text entities

- **Genes:** CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}
- **Diseases:** hematologic malignancy (MESH:D019337), ALL (MESH:D054198), toxicity (MESH:D064420), B-cell ALL (MESH:D015456)
- **Chemicals:** blinatumomab (MESH:C510808)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12891086/full.md

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Source: https://tomesphere.com/paper/PMC12891086