Advanced Pediatric Center, Pediatric Hematology-Oncology Unit, Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Pediatr Blood Cancer. 2012 Sep;59(3):481-4. doi: 10.1002/pbc.23389. Epub 2011 Nov 2.
Long-term adverse effects of Imatinib in children with chronic myeloid leukemia (CML) are uncertain. The aim was to study the effect of imatinib on growth in children with CML.
Children ≤13 years of age at diagnosis were enrolled retrospectively, from 2004 to 2011, from a single center in India. Patients who received imatinib for >1 year were included for growth assessment. Height standard deviation scores (SDS) were derived from WHO-AnthroPlus, a global growth monitoring tool.
Thirty-four children received imatinib. Twenty children fulfilled the criteria for assessment of growth. Median age was 10 years (range: 2-13). Of 20 children, 13 were prepubertal at commencement of imatinib. The mean duration of imatinib in 20 children was 61.3 ± 16.2 months (range: 31-83). No patient was treated with a second-generation tyrosine kinase inhibitor or a stem cell transplant. Highly significant reduction in height SDS's was observed (P = 0.002 at 5th year). Children who started imatinib therapy after the onset of puberty were immune to this adverse effect (P = 0.448 and 0.003 at 5th year of treatment for pubertal and prepubertal children, respectively). The 5-year survival probability of 33 children who received imatinib in chronic phase was 80% with a median survival time of 60 months (mean: 70.2; 95% CI: 60-80.5).
Growth retardation is a significant adverse effect of imatinib in children with CML. The failure to gain appropriate height was most discernible when imatinib was initiated in the prepubertal period. Etiology and remedial measures need to be investigated.
伊马替尼治疗儿童慢性髓性白血病(CML)的长期不良影响尚不确定。本研究旨在探讨伊马替尼对儿童 CML 患者生长的影响。
回顾性纳入 2004 年至 2011 年在印度某单一中心接受治疗的诊断时年龄≤13 岁的 CML 患儿。纳入标准为接受伊马替尼治疗>1 年的患儿。采用全球生长监测工具 WHO-AnthroPlus 计算身高标准差评分(SDS)。
共 34 例患儿接受伊马替尼治疗。20 例患儿符合生长评估标准。中位年龄为 10 岁(范围:2-13 岁)。13 例患儿在开始伊马替尼治疗时处于青春前期。20 例患儿伊马替尼的平均治疗时间为 61.3±16.2 个月(范围:31-83 个月)。无患儿接受第二代酪氨酸激酶抑制剂或干细胞移植治疗。第 5 年时,身高 SDS 显著降低(P=0.002)。青春期后开始伊马替尼治疗的患儿对该不良反应具有免疫力(青春期和青春前期患儿在第 5 年治疗时,P=0.448 和 0.003)。接受伊马替尼治疗的 33 例慢性期患儿的 5 年生存率为 80%,中位生存时间为 60 个月(平均:70.2;95%CI:60-80.5)。
生长迟缓是 CML 儿童接受伊马替尼治疗的一个显著不良影响。当伊马替尼在青春前期开始使用时,身高增长不足最为明显。需要进一步研究其病因和补救措施。