Lie S O, Abrahamsson J, Clausen N, Forestier E, Hasle H, Hovi L, Jonmundsson G, Mellander L, Siimes M A, Yssing M, Zeller B, Gustafsson G
Department of Pediatrics, University Hospital, Rikshospitalet, Oslo, Norway.
Leukemia. 2005 Dec;19(12):2090-100. doi: 10.1038/sj.leu.2403962.
In all, 447 children with acute myeloid leukaemia (AML) have been treated on three consecutive NOPHO studies from July 1984 to December 2001. NOPHO-AML 84 was of moderate intensity with an induction of three courses of cytarabine, 6-thioguanine and doxorubicin followed by four consolidation courses with high-dose cytarabine. The 5-year event-free survival (EFS), disease free survival (DFS) and overall survival (OS) were 29, 37 and 38%. NOPHO-AML 88 was of high intensity with the addition of etoposide and mitoxantrone in selected courses during induction and consolidation. The interval between the induction courses should be as short as possible, that is, time intensity was introduced. The 5-year EFS, DFS and OS were 41, 48 and 46%. In NOPHO-AML 93, the treatment was stratified according to response to first induction course. The protocol utilised the same induction blocks as NOPHO-AML 88, but after the first block, children with a hypoplastic, nonleukaemic bone marrow were allowed to recover before the second block. Consolidation was identical with NOPHO-AML 88. The 5-year EFS, DFS and OS in NOPHO-AML 93 were 48, 52 and 65%. The new NOPHO-AML protocol has been based on experiences from previous protocols with stratification of patients with regard to in vivo response and specific cytogenetic aberrations.
从1984年7月至2001年12月,共有447名急性髓系白血病(AML)患儿接受了连续三项北欧儿童血液肿瘤学会(NOPHO)研究的治疗。NOPHO - AML 84方案强度适中,诱导治疗采用三个疗程的阿糖胞苷、6 - 硫鸟嘌呤和阿霉素,随后用大剂量阿糖胞苷进行四个疗程的巩固治疗。5年无事件生存率(EFS)、无病生存率(DFS)和总生存率(OS)分别为29%、37%和38%。NOPHO - AML 88方案强度高,在诱导和巩固治疗的特定疗程中加入了依托泊苷和米托蒽醌。诱导疗程之间的间隔应尽可能短,即引入了时间强度的概念。5年EFS、DFS和OS分别为41%、48%和46%。在NOPHO - AML 93方案中,治疗根据对第一个诱导疗程的反应进行分层。该方案采用了与NOPHO - AML 88相同的诱导方案,但在第一个疗程后,骨髓增生低下、无白血病的患儿在第二个疗程前可恢复。巩固治疗与NOPHO - AML 88相同。NOPHO - AML 93方案的5年EFS、DFS和OS分别为48%、52%和65%。新的NOPHO - AML方案基于以往方案的经验,根据患者的体内反应和特定细胞遗传学异常进行分层。