Creutzig U, Zimmermann M, Ritter J, Reinhardt D, Hermann J, Henze G, Jürgens H, Kabisch H, Reiter A, Riehm H, Gadner H, Schellong G
Department of Haematology, Oncology, University Children's Hospital, Münster, Germany. ursula.creutzig.de
Leukemia. 2005 Dec;19(12):2030-42. doi: 10.1038/sj.leu.2403920.
A total of 1111 children with acute myeloblastic leukaemia (AML) were treated in four consecutive Berlin-Frankfurt-Münster (BFM) studies from 1978 to 1998. The first cooperative trial AML-BFM 78 established intensive chemotherapy with seven drugs, CNS irradiation and 2-year maintenance, achieving a long-term survival (overall survival (OS)) of 40%. Induction intensification in AML-BFM 83 resulted in significant improvement of disease-free survival (DFS). The risk of haemorrhage, especially in children with hyperleukocytosis, proved the high relevance of supportive care. In AML-BFM 87, the benefit of CNS irradiation in preventing CNS/systemic relapses was demonstrated. In AML-BFM 93, the introduction of idarubicin during first induction followed by intensification with HAM increased the 5-year EFS, DFS and OS to 50+/-2, 61+/-3 and 57+/-2%, respectively. Stem cell transplantation (SCT), as applied in high-risk patients with a matched related donor, did not significantly improve the outcome compared to chemotherapy alone. In spite of treatment intensification, the therapy-related death rate decreased from trial to trial, mainly during induction. The future aim is to reduce long-term sequelae, especially cardiotoxicity, by administration of less cardiotoxic drugs, and toxicity of SCT by risk-adapted indications. The AML-BFM studies performed in three European countries with >70 cooperating centres have significantly improved the outcome in AML children; nevertheless, increasing experience with these intensive treatment regimens is of fundamental importance to reduce fatal complications.
1978年至1998年期间,在四项连续的柏林-法兰克福-明斯特(BFM)研究中,共对1111名急性髓细胞白血病(AML)患儿进行了治疗。第一项合作试验AML-BFM 78采用七种药物进行强化化疗、中枢神经系统放疗及2年维持治疗,长期生存率(总生存率(OS))达到40%。AML-BFM 83中的诱导强化治疗使无病生存率(DFS)显著提高。出血风险,尤其是高白细胞血症患儿的出血风险,证明了支持治疗的高度相关性。在AML-BFM 87中,证实了中枢神经系统放疗在预防中枢神经系统/全身复发方面的益处。在AML-BFM 93中,首次诱导期间引入伊达比星并随后用HAM强化治疗,使5年无事件生存率(EFS)、DFS和OS分别提高到50±2%、61±3%和57±2%。对于有匹配相关供体的高危患者应用的干细胞移植(SCT),与单纯化疗相比,并未显著改善治疗结果。尽管治疗强度增加,但治疗相关死亡率在各试验中呈下降趋势,主要发生在诱导期。未来的目标是通过使用心脏毒性较小的药物来减少长期后遗症,尤其是心脏毒性,并通过根据风险调整适应症来降低SCT的毒性。在三个欧洲国家的70多个合作中心开展的AML-BFM研究显著改善了AML患儿的治疗结果;然而,增加对这些强化治疗方案的经验对于减少致命并发症至关重要。