Adverse effects of imatinib in children with chronic myelogenous leukemia

© 2016 Japan Pediatric Society Background: Imatinib mesylate (IM) is a selective tyrosine kinase inhibitor and is approved for indefinite treatment of pediatric chronic myelogenous leukemia (CML). Potential side-effects regarding growth failure and bone metabolism have been reported but data are sti...

Full description

Saved in:
Bibliographic Details
Main Authors: Worawut Choeyprasert, Thitinun Yansomdet, Rungrote Natesirinilkul, Karn Wejaphikul, Pimlak Charoenkwan
Format: Journal
Published: 2018
Subjects:
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85005810433&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/57736
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-57736
record_format dspace
spelling th-cmuir.6653943832-577362018-09-05T03:48:56Z Adverse effects of imatinib in children with chronic myelogenous leukemia Worawut Choeyprasert Thitinun Yansomdet Rungrote Natesirinilkul Karn Wejaphikul Pimlak Charoenkwan Medicine © 2016 Japan Pediatric Society Background: Imatinib mesylate (IM) is a selective tyrosine kinase inhibitor and is approved for indefinite treatment of pediatric chronic myelogenous leukemia (CML). Potential side-effects regarding growth failure and bone metabolism have been reported but data are still scarce in pediatric CML. Methods: Six chronic-phase CML children on IM treatment with a median age of 9.87 years (range, 5.33–12.67 years) were enrolled in the study. Growth, bone mineral density (BMD), bone parameters, 25(OH)-vitamin D3 (25-OHD3) and blood tests including parathyroid hormone, insulin-like growth factor-1 (IGF-1), IGF binding protein 3, thyroid function test and sex hormones were assessed. Results: Median duration of IM treatment was 78.5 months. Height velocity was suppressed during the first 30 months of treatment and improved gradually afterwards. Two patients (33.3%) had decreased lumbar spine BMD z-scores (<1.5 SD). Patients with decreased BMD had higher mean IM exposure time than those with normal BMD. The majority of patients (n = 5) had low 25-OHD3 (<30 ng/mL), but there was no correlation between BMD and 25-OHD3 status. Other blood tests were normal. Conclusions: This study supports and confirms the need for monitoring the side-effects of IM treatment on growth, bone density and vitamin D status in pediatric CML. Prolonged IM treatment was associated with low BMD without disturbing bone parameters. There was high prevalence of vitamin D insufficiency. Therefore, the beneficial effect of vitamin D supplement should be explored with regard to the effects on height velocity and BMD in CML patients with vitamin D insufficiency. 2018-09-05T03:48:56Z 2018-09-05T03:48:56Z 2017-03-01 Journal 1442200X 13288067 2-s2.0-85005810433 10.1111/ped.13136 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85005810433&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/57736
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine
spellingShingle Medicine
Worawut Choeyprasert
Thitinun Yansomdet
Rungrote Natesirinilkul
Karn Wejaphikul
Pimlak Charoenkwan
Adverse effects of imatinib in children with chronic myelogenous leukemia
description © 2016 Japan Pediatric Society Background: Imatinib mesylate (IM) is a selective tyrosine kinase inhibitor and is approved for indefinite treatment of pediatric chronic myelogenous leukemia (CML). Potential side-effects regarding growth failure and bone metabolism have been reported but data are still scarce in pediatric CML. Methods: Six chronic-phase CML children on IM treatment with a median age of 9.87 years (range, 5.33–12.67 years) were enrolled in the study. Growth, bone mineral density (BMD), bone parameters, 25(OH)-vitamin D3 (25-OHD3) and blood tests including parathyroid hormone, insulin-like growth factor-1 (IGF-1), IGF binding protein 3, thyroid function test and sex hormones were assessed. Results: Median duration of IM treatment was 78.5 months. Height velocity was suppressed during the first 30 months of treatment and improved gradually afterwards. Two patients (33.3%) had decreased lumbar spine BMD z-scores (<1.5 SD). Patients with decreased BMD had higher mean IM exposure time than those with normal BMD. The majority of patients (n = 5) had low 25-OHD3 (<30 ng/mL), but there was no correlation between BMD and 25-OHD3 status. Other blood tests were normal. Conclusions: This study supports and confirms the need for monitoring the side-effects of IM treatment on growth, bone density and vitamin D status in pediatric CML. Prolonged IM treatment was associated with low BMD without disturbing bone parameters. There was high prevalence of vitamin D insufficiency. Therefore, the beneficial effect of vitamin D supplement should be explored with regard to the effects on height velocity and BMD in CML patients with vitamin D insufficiency.
format Journal
author Worawut Choeyprasert
Thitinun Yansomdet
Rungrote Natesirinilkul
Karn Wejaphikul
Pimlak Charoenkwan
author_facet Worawut Choeyprasert
Thitinun Yansomdet
Rungrote Natesirinilkul
Karn Wejaphikul
Pimlak Charoenkwan
author_sort Worawut Choeyprasert
title Adverse effects of imatinib in children with chronic myelogenous leukemia
title_short Adverse effects of imatinib in children with chronic myelogenous leukemia
title_full Adverse effects of imatinib in children with chronic myelogenous leukemia
title_fullStr Adverse effects of imatinib in children with chronic myelogenous leukemia
title_full_unstemmed Adverse effects of imatinib in children with chronic myelogenous leukemia
title_sort adverse effects of imatinib in children with chronic myelogenous leukemia
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85005810433&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/57736
_version_ 1681424934283247616