Departments of Paediatric Oncology/Haematology, Beatrix Children's Hospital, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Departments of Paediatric Oncology/Haematology, Poitiers University Hospital, Poitiers, France.
Br J Haematol. 2019 May;185(4):718-724. doi: 10.1111/bjh.15826. Epub 2019 Mar 6.
This international study aimed to assess the effect of imatinib discontinuation in paediatric patients with chronic myeloid leukaemia (CML) after deep molecular remission (DMR) had been achieved and maintained for at least 2 years. The primary endpoint of this analysis was the molecular relapse-free survival, estimated by the non-parametric Kaplan-Meier method. Major endpoint was the estimated rate of patients without molecular relapse at 6 months. Fourteen patients were enrolled; 4 patients maintained DMR with a follow-up of 24 (two patients), 34 and 66 months, respectively, whereas 10 patients relapsed. All molecular relapses occurred within 6 months (median 3 months, range 1-6) after imatinib discontinuation. The overall probability of maintaining DMR at 6 months was 28·6%. No parameters associated with molecular relapse could be identified. Keeping in mind the rarity of paediatric CML, which contributed to the small size of the cohort, our findings illustrate that imatinib cessation after sustained DMR is successful in only limited numbers of patients, whereas much higher rates are reported in adult patients. Further research is needed to extend the cohort of paediatric CML patients who might achieve treatment-free remission with an ideal prerequisite of predicting the occurrence of molecular relapse l after imatinib cessation.
这项国际研究旨在评估在慢性髓性白血病(CML)患儿达到深度分子缓解(DMR)并维持至少 2 年后停止伊马替尼治疗的效果。本分析的主要终点是通过非参数 Kaplan-Meier 方法估计的无分子复发生存。主要终点是在 6 个月时无分子复发的患者估计率。共纳入 14 名患者;4 名患者维持 DMR,随访 24(2 名患者)、34 和 66 个月,而 10 名患者复发。所有分子复发均发生在伊马替尼停药后 6 个月内(中位数 3 个月,范围 1-6)。6 个月时维持 DMR 的总体概率为 28.6%。未发现与分子复发相关的参数。考虑到儿童 CML 的罕见性,这导致了队列规模较小,我们的研究结果表明,在持续 DMR 后停止伊马替尼治疗仅在少数患者中取得成功,而在成年患者中报告的比率要高得多。需要进一步研究来扩大可能在停药后达到无治疗缓解的儿童 CML 患者队列,其理想的前提是预测伊马替尼停药后分子复发的发生。