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Updated: Jun 2, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Prepubertal Initiation of Imatinib is Associated with Reduced Final Height in Children with Chronic Myeloid Leukemia
Rohit Sadanand1, Rama Walia2, Swetha Palla1
1Pediatric Hematology-Oncology Unit, Department of Pediatrics, Advanced Pediatric Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Insights
Imatinib treatment for pediatric chronic myeloid leukemia (CML) can cause growth deceleration. Final adult height may be reduced, especially if therapy begins before puberty, despite adolescent catch-up growth.
Area of Science:
- Pediatric Oncology
- Hematology
- Endocrinology
Background:
- Imatinib is a tyrosine kinase inhibitor used to treat chronic myeloid leukemia (CML).
- Growth deceleration has been observed in children receiving imatinib, but long-term effects on final height are less understood.
Purpose of the Study:
- To evaluate the impact of prolonged imatinib therapy on linear growth in children with CML who have reached skeletal maturity.
- To determine if the timing of imatinib initiation relative to pubertal development influences final height.
Main Methods:
- A cross-sectional study included 13 patients with CML diagnosed before age 13 and who had attained skeletal maturity.
- Data collected included anthropometry, sexual maturity, bone age, and longitudinal height from medical records.
- Height z-scores at diagnosis and skeletal maturity were compared with population-specific growth charts.
Main Results:
- Mean height z-score decreased from -0.6 at diagnosis to -1.1 at skeletal maturity (p=0.04).
- Patients initiating imatinib before the pubertal growth spurt showed a significant decline in height z-score (-0.5 to -1.3, p=0.03).
- No significant height z-score decline was observed in those starting imatinib after the pubertal growth spurt (p=0.60).
Conclusions:
- Prolonged imatinib therapy in children with CML leads to reduced final height, particularly when initiated before puberty.
- Despite some catch-up growth during adolescence, final height z-scores remain reduced at skeletal maturity.
- This study provides long-term follow-up data on the effects of imatinib on growth in pediatric CML patients.
Abstract:
Imatinib in children with chronic myeloid leukemia (CML) is associated with growth deceleration. However, the long-term impact on final height remains less clear. The aim was to evaluate the effect of prolonged imatinib on linear growth at skeletal maturity. A cross-sectional study was conducted at a single center (2020-2021). Patients with chronic-phase CML on imatinib, diagnosed before 13 years and who had attained skeletal maturity at enrollment, were included. Anthropometry, sexual maturity rating, bone age, and evaluation for causes of short stature were performed. Longitudinal height data were retrieved from clinic records and compared with population-specific growth charts. Of 46 screened patients, 13 fulfilled the inclusion criteria. Mean age at diagnosis and enrollment was 9.3 ± 2.3 and 23.7 ± 2.6 years. The median duration of imatinib therapy was 14.3 years (IQR: 14.2-16), with 184.4 patient-years of follow-up. Mean height z-score declined from -0.6 ± 1.2 at diagnosis to -1.1 ± 0.9 at maturity (p = 0.04). In those administered imatinib before the onset of pubertal growth spurt, the decline was significant (-0.5 ± 0.6 to -1.3 ± 0.6, p = 0.03), compared to those administered after the pubertal growth spurt (p = 0.60). In one of the longest follow-up cohorts of children with CML reported to date, imatinib resulted in growth deceleration, particularly when initiated before the onset of pubertal growth spurt. Despite catch-up growth during adolescence, final height z-scores remained reduced at skeletal maturity.
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