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Updated: May 1, 2026

Murine Model of Leukemia Relapse to Induction Chemotherapy for Acute Lymphoblastic Leukemia
Published on: October 17, 2025
The evolution of clinical trials for infant acute lymphoblastic leukemia
R S Kotecha1, N G Gottardo1, U R Kees2
11] Department of Haematology and Oncology, Princess Margaret Hospital for Children, Perth, Western Australia, Australia [2] Telethon Institute for Child Health Research, University of Western Australia, Perth, Western Australia, Australia [3] School of Paediatrics and Child Health, University of Western Australia, Perth, Western Australia, Australia.
Insights
Infant acute lymphoblastic leukemia (ALL) survival has plateaued despite advances. New prognostic markers, innovative therapies, and unified international trials are crucial for improving outcomes in infant ALL patients.
Area of Science:
- Pediatric Oncology
- Hematology
- Leukemia Research
Background:
- Infant acute lymphoblastic leukemia (ALL) presents a poorer prognosis than in older children.
- Survival rates for infant ALL have stagnated in recent years despite initial therapeutic improvements.
- Historical treatment on childhood ALL protocols highlighted the need for infant-specific approaches.
Purpose of the Study:
- To review the progress and challenges in treating infant acute lymphoblastic leukemia (ALL).
- To identify key areas for future research and therapeutic development in infant ALL.
- To emphasize the need for a unified international approach to improve outcomes.
Main Methods:
- Review of historical and current pediatric cooperative group trials for infant ALL.
- Analysis of prognostic factors and treatment strategies, including CNS prophylaxis.
- Evaluation of the balance between treatment efficacy and toxicity.
Main Results:
- Elimination of cranial radiotherapy in favor of intrathecal and high-dose systemic therapy for CNS prophylaxis.
- Identification of adverse prognostic factors like MLL rearrangement and young age for risk stratification.
- Chemotherapy intensification has reached limits without improving survival due to relapse and toxicity equilibrium.
Conclusions:
- Further improvements in infant ALL survival require novel prognostic markers and innovative therapies.
- Establishing the role of stem cell transplantation and optimizing relapsed/refractory disease treatment are critical.
- A unified international trial is essential to overcome limitations and advance treatment for infant ALL.
Abstract:
Acute lymphoblastic leukemia (ALL) in infants has a significantly inferior outcome in comparison with older children. Despite initial improvements in survival of infants with ALL since establishment of the first pediatric cooperative group ALL trials, the poor outcome has plateaued in recent years. Historically, infants were treated on risk-adapted childhood ALL protocols. These studies were pivotal in identifying the need for infant-specific protocols, delineating prognostic categories and the requirement for a more unified approach between study groups to overcome limitations in accrual because of low incidence. This subsequently led to the development of collaborative infant-specific studies. Landmark outcomes have included the elimination of cranial radiotherapy following the discovery of intrathecal and high-dose systemic therapy as a superior and effective treatment strategy for central nervous system disease prophylaxis, with improved neurodevelopmental outcome. Universal prospective identification of independent adverse prognostic factors, including presence of a mixed lineage leukemia rearrangement and young age, has established the basis for risk stratification within current trials. The infant-specific trials have defined limits to which conventional chemotherapeutic agents can be intensified to optimize the balance between treatment efficacy and toxicity. Despite variations in therapeutic intensity, there has been no recent improvement in survival due to the equilibrium between relapse and toxicity. Ultimately, to improve the outcome for infants with ALL, key areas still to be addressed include identification and adaptation of novel prognostic markers and innovative therapies, establishing the role of hematopoietic stem cell transplantation in first complete remission, treatment strategies for relapsed/refractory disease and monitoring and timely intervention of late effects in survivors. This would be best achieved through a single unified international trial.
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