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Updated: Mar 6, 2026

Murine Model of Leukemia Relapse to Induction Chemotherapy for Acute Lymphoblastic Leukemia
Published on: October 17, 2025
Treatment delay and the risk of relapse in pediatric acute lymphoblastic leukemia
Amelia Yeoh1, Anna Collins2, Kahlia Fox2
1a Discipline of Paediatrics , University of Adelaide , Adelaide , South Australia , Australia.
Insights
Treatment delays in pediatric acute lymphoblastic leukemia (ALL) due to toxicity did not increase relapse risk overall. However, longer delays during maintenance therapy showed a trend towards fewer relapses in children with ALL.
Area of Science:
- Pediatric Oncology
- Hematology
- Clinical Research
Background:
- Toxicity-induced chemotherapy interruptions are common in pediatric acute lymphoblastic leukemia (ALL).
- Concerns exist that these treatment delays may negatively impact patient outcomes.
- Previous studies suggest poorer outcomes with reduced therapy compliance.
Purpose of the Study:
- To investigate the association between chemotherapy treatment delays and relapse risk in pediatric ALL patients.
- To analyze delays during different phases of treatment: total, intensive, and maintenance.
Main Methods:
- Retrospective review of 141 pediatric ALL patients treated between 2003 and 2013.
- Analysis of cumulative chemotherapy delay lengths during total, intensive, and maintenance phases.
- Comparison of relapse risk between patients with shorter versus longer treatment delays (median and quartile analysis).
Main Results:
- No significant difference in relapse risk was observed for delays during the total treatment duration or the intensive phase.
- A trend towards reduced relapse risk was noted with longer delays during the maintenance phase.
- A statistically significant decrease in relapses was found in patients experiencing the longest delays during maintenance therapy.
Conclusions:
- Chemotherapy delays due to toxicity in pediatric ALL do not universally increase relapse risk.
- Extended treatment delays during the maintenance phase may be associated with a lower risk of relapse in pediatric ALL.
- Further research is warranted to understand the mechanisms behind this observed association.
Abstract:
Delays or interruptions in chemotherapy due to toxicity such as neutropenia or severe infections are common in the treatment of pediatric acute lymphoblastic leukemia (ALL). Based on the reports of worse outcomes in children with poorer compliance with therapy, there has been concern that toxicity-induced therapy interruptions could also compromise treatment outcome. In a retrospective study of treatment delays in our hospital between 2003 and 2013, the case notes of 141 patients were reviewed. The cumulative lengths of delays during the whole length of chemotherapy, during the intensive phase of treatment, and during maintenance treatment were analyzed. Within these categories, delays were split between less and more than the median value. The risk of relapse did not differ between patients with a longer or shorter delay during the total length of treatment or during the intensive phase. In addition, there was a trend when comparing patients above vs below the mean in length of treatment delays during maintenance, and there was a statistically significant difference in relapses when comparing patients in the lowest and highest quartiles of maintenance delays, with fewer relapses among those patients in the highest quartile for treatment delays.
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