Department of Paediatrics, The University Hospital Rigshospitalet, Copenhagen, Denmark.
Eur J Haematol. 2013 Mar;90(3):187-94. doi: 10.1111/ejh.12051. Epub 2013 Jan 20.
Children with poor response acute myeloid leukaemia (AML) generally have a very poor outcome. Allogeneic stem cell transplantation (SCT) is often recommended for these children but the benefit is unclear. The aim of this study was to investigate survival for poor response AML patients treated with SCT.
Treatment was given according to the NOPHO-AML 2004 protocol. All patients received AIET (Cytarabine, Idarubicin, Etoposide, Thioguanine) and AM (Cytarabine, Mitoxantrone) as induction. We included poor response defined as > 15% blasts on day 15 after AIET (n = 17) or > 5% blasts after AM (n = 14, refractory disease). Poor response patients received intensively timed induction and proceeded to SCT when a donor was available.
Thirty-one of 267 evaluable patients (12%) had a poor response. SCT was performed in 25; using matched unrelated donors in 13, matched sibling donors in 6, cord blood donor in 4, and haploidentical donor in two. The median follow-up for the 31 poor responding patients was 2.6 years (range 0.4 - 8.1 years) and 3-year probability of survival 70% (95% CI 59-77%).
The poor responders in the NOPHO-AML 2004 protocol had a favourable prognosis treated with time-intensive induction followed by SCT.
对治疗反应不佳的急性髓细胞白血病(AML)患儿,通常预后极差。对于这些患儿,常常推荐异体造血干细胞移植(SCT),但获益并不明确。本研究旨在评估对治疗反应不佳的 AML 患儿行 SCT 治疗的生存情况。
根据北欧儿童血液和骨髓移植组 AML 2004 方案进行治疗。所有患者均接受 AIET(阿糖胞苷、伊达比星、依托泊苷、硫鸟嘌呤)和 AM(阿糖胞苷、米托蒽醌)诱导治疗。我们将诱导治疗第 15 天骨髓原始细胞>15%(n = 17)或 AM 后骨髓原始细胞>5%(n = 14,难治性疾病)定义为治疗反应不佳。治疗反应不佳的患者接受强化诱导治疗,待供者合适时行 SCT。
在 267 例可评估患者中,有 31 例(12%)为治疗反应不佳。25 例患者行 SCT,其中 13 例接受了相合无关供者、6 例接受了相合同胞供者、4 例接受了脐带血供者、2 例接受了单倍体相合供者。31 例治疗反应不佳的患者中位随访时间为 2.6 年(范围 0.4-8.1 年),3 年生存率为 70%(95%CI 59-77%)。
北欧儿童血液和骨髓移植组 AML 2004 方案中治疗反应不佳的患者经强化诱导治疗后行 SCT 治疗,预后良好。