Suttorp M
Department of Paediatrics, University Hospital, Dresden, Germany.
Bone Marrow Transplant. 2008 Oct;42 Suppl 2:S40-6. doi: 10.1038/bmt.2008.282.
Allogeneic haematopoietic SCT (HSCT) induces CRs in most patients with CML. With the excellent short-term treatment results induced by imatinib (IMA), attitudes have changed and only a minority of children are now transplanted upfront. This review addresses the role of IMA in children with CML, focusing on the starting dose of IMA, possible adverse effects, timing of HSCT in children, duration of IMA treatment and monitoring of treatment efficacy to unravel failure of early treatment of IMA as well as treatment of CML relapse after HSCT. As the paediatric experience with IMA is still very limited, many answers and algorithms are adapted from CML in adults. Basically, HSCT should be postponed to achieve an optimal tumour cell reduction by IMA treatment. Children with a low-risk EBMT score should undergo HSCT within 2 years after diagnosis to avoid prolonged exposure and unknown late effects of IMA. Without a perfectly HLA-matched donor, HSCT may be postponed until CML becomes refractory to IMA. As realized in the presently activated international trial CML-paed II, this approach represents a risk-adapted therapy with the benefit of being tailored to the needs and profile of an individual patient.
异基因造血干细胞移植(HSCT)可使大多数慢性粒细胞白血病(CML)患者获得完全缓解(CR)。由于伊马替尼(IMA)诱导的短期治疗效果极佳,人们的态度已经发生了变化,现在只有少数儿童接受前期移植。本综述探讨了IMA在儿童CML中的作用,重点关注IMA的起始剂量、可能的不良反应、儿童HSCT的时机、IMA治疗的持续时间以及治疗疗效监测,以阐明IMA早期治疗失败以及HSCT后CML复发的治疗情况。由于儿童使用IMA的经验仍然非常有限,许多答案和方案都借鉴了成人CML的经验。基本上,应推迟HSCT,以便通过IMA治疗实现最佳的肿瘤细胞减少。欧洲血液与骨髓移植协会(EBMT)低风险评分的儿童应在诊断后2年内接受HSCT,以避免IMA的长期暴露和未知的晚期影响。如果没有完全匹配的HLA供体,HSCT可推迟至CML对IMA难治时进行。正如目前正在进行的国际试验CML-paed II所认识到的,这种方法代表了一种风险适应性治疗,其好处是能够根据个体患者的需求和情况进行定制。