Background Imatinib mesylate, a tyrosine kinase inhibitor, is used in the treatment of chronic myelogeneous leukemia (CML). Given its ease of administration and manageable side effects in adults, imatinib mesylate was introduced as therapy for pediatric CML. Recently published case reports describe growth deceleration in children treated with imatinib. This study details the growth phenotype of seven pediatric patients maintained in remission on imatnib mesylate over an extended period of time. Procedure This study is a retrospective chart review of pediatric patients with CML at Oregon Health & Science University treated with imatinib. Height, weight, and body mass index (BMI) measurements were collected before and during treatment. Median standard deviation scores (SDS) were analyzed by Wilcoxon Rank-Sum test and Wilcoxon signed rank cohort analysis. Results Individual patient analysis demonstrated five of seven subjects with a statistically significant decrease in height SDS pre versus during treatment. The whole group analysis showed a trend to significance for difference in median height SDS pre and during treatment (P?=?0.078). Bone age was delayed in all four patients in whom bone ages were obtained. IGF-1, IGFBP-3, and thyroid levels during treatment were normal. Four patients experienced an improvement in height SDS during puberty. However, three patients approaching near final adult height failed to achieve genetic height potential determined by mid-parental target height. Conclusion Growth in children with CML appears to be adversely impacted by imatinib therapy. BMI and IGF-1/IGFBP-3 are maintained during treatment, suggesting a direct effect of imatinib on the growth plate. Pediatr Blood Cancer 2012; 59: 840845. (C) 2012 Wiley Periodicals, Inc.
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All India Inst Med Sci, Dept Med Oncol, Inst Rotary Canc Hosp, New Delhi 110029, IndiaAll India Inst Med Sci, Dept Med Oncol, Inst Rotary Canc Hosp, New Delhi 110029, India
Lokeshwar, N
Kumar, L
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All India Inst Med Sci, Dept Med Oncol, Inst Rotary Canc Hosp, New Delhi 110029, IndiaAll India Inst Med Sci, Dept Med Oncol, Inst Rotary Canc Hosp, New Delhi 110029, India
Kumar, L
Kumari, M
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All India Inst Med Sci, Dept Med Oncol, Inst Rotary Canc Hosp, New Delhi 110029, IndiaAll India Inst Med Sci, Dept Med Oncol, Inst Rotary Canc Hosp, New Delhi 110029, India
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Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, JapanKomagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, Japan
Narukawa, Kensuke
Kakihana, Kazuhiko
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Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, JapanKomagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, Japan
Kakihana, Kazuhiko
Fujiwara, Takashi
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Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Gastroenterol, Tokyo, JapanKomagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, Japan
Fujiwara, Takashi
Kobayashi, Takeshi
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Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, JapanKomagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, Japan
Kobayashi, Takeshi
Doki, Noriko
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Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, JapanKomagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, Japan
Doki, Noriko
Sakamaki, Hisashi
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Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, JapanKomagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, Japan
Sakamaki, Hisashi
Ohashi, Kazuteru
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Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, JapanKomagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Div Hematol, Tokyo, Japan