TY - JOUR
T1 - Distinct impact of imatinib on growth at prepubertal and pubertal ages of children with chronic myeloid leukemia
AU - Shima, Haruko
AU - Tokuyama, Mika
AU - Tanizawa, Akihiko
AU - Tono, Chikako
AU - Hamamoto, Kazuko
AU - Muramatsu, Hideki
AU - Watanabe, Akihiro
AU - Hotta, Noriko
AU - Ito, Masaki
AU - Kurosawa, Hidemitsu
AU - Kato, Koji
AU - Tsurusawa, Masahito
AU - Horibe, Keizo
AU - Shimada, Hiroyuki
N1 - Funding Information:
Supported by a grant for clinical cancer research from the Ministry of Health, Labor, and Welfare , Japan. The authors declare no conflicts of interest.
PY - 2011/10
Y1 - 2011/10
N2 - Objective: To determine the extent of growth impairment resulting from imatinib treatment in children with chronic myeloid leukemia (CML). Study design: Clinical records of 48 chronic-phase CML children administered imatinib as the first-line therapy between 2001 and 2006 were analyzed retrospectively. Cumulative change in height was assessed using the height height-SDS and converted height data from age- and sex-adjusted Japanese norms. Results: A decrease in height-SDS was observed in 72.9% of children, with a median maximum reduction in height-SDS of 0.61 during imatinib treatment. Median follow-up time was 34 months (range, 10-88 months). Growth impairment was seen predominantly in children who started imatinib at a prepubertal age compared with those who started at pubertal age. Growth velocity tended to recuperate in prepubertal children with growth impairment, as they reached pubertal age, suggesting that imatinib had little impact on growth during puberty. Conclusions: Growth impairment was a major adverse effect of long-term imatinib treatment in children with CML. We report the distinct inhibitory effect of imatinib on growth in prepubertal and pubertal children with CML. We should be aware of growth deceleration in children, especially in young children given imatinib before puberty and subjected to prolonged exposure.
AB - Objective: To determine the extent of growth impairment resulting from imatinib treatment in children with chronic myeloid leukemia (CML). Study design: Clinical records of 48 chronic-phase CML children administered imatinib as the first-line therapy between 2001 and 2006 were analyzed retrospectively. Cumulative change in height was assessed using the height height-SDS and converted height data from age- and sex-adjusted Japanese norms. Results: A decrease in height-SDS was observed in 72.9% of children, with a median maximum reduction in height-SDS of 0.61 during imatinib treatment. Median follow-up time was 34 months (range, 10-88 months). Growth impairment was seen predominantly in children who started imatinib at a prepubertal age compared with those who started at pubertal age. Growth velocity tended to recuperate in prepubertal children with growth impairment, as they reached pubertal age, suggesting that imatinib had little impact on growth during puberty. Conclusions: Growth impairment was a major adverse effect of long-term imatinib treatment in children with CML. We report the distinct inhibitory effect of imatinib on growth in prepubertal and pubertal children with CML. We should be aware of growth deceleration in children, especially in young children given imatinib before puberty and subjected to prolonged exposure.
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U2 - 10.1016/j.jpeds.2011.03.046
DO - 10.1016/j.jpeds.2011.03.046
M3 - Article
C2 - 21592517
AN - SCOPUS:80052790433
SN - 0022-3476
VL - 159
SP - 676
EP - 681
JO - Journal of Pediatrics
JF - Journal of Pediatrics
IS - 4
ER -