Morra Enrica, Barosi Giovanni, Bosi Alberto, Ferrara Felicetto, Locatelli Franco, Marchetti Monia, Martinelli Giovanni, Mecucci Cristina, Vignetti Marco, Tura Sante
Division of Hematology, Niguarda Ca'Granda Hospital, Milan, Italy.
Haematologica. 2009 Jan;94(1):102-12. doi: 10.3324/haematol.13166. Epub 2008 Nov 10.
As many options are now available to treat patients with de novo acute myeloid leukemia, the Italian Society of Hematology and two affiliated societies (SIES and GITMO) commissioned project to an Expert Panel aimed at developing clinical practice guidelines for acute myeloid leukemia treatment. After systematic comprehensive literature review, the Expert Panel formulated recommendations for the management of primary acute myeloid leukemia (with the exception of acute promyelocytic leukemia) and graded them according to the supporting evidence. When evidence was lacking, consensus-based statements have been added. First-line therapy for all newly diagnosed patients eligible for intensive treatment should include one cycle of induction with standard dose cytarabine and an anthracycline. After achieving complete remission, patients aged less than 60 years should receive consolidation therapy including high-dose cytarabine. Myeloablative allogeneic stem cell transplantation from an HLA-compatible sibling should be performed in first complete remission: 1) in children with intermediate-high risk cytogenetics or who achieved first complete remission after the second course of therapy; 2) in adults less than 40 years with an intermediate-risk; in those aged less than 55 years with either high-risk cytogenetics or who achieved first complete remission after the second course of therapy. Stem cell transplantation from an unrelated donor is recommended to be performed in first complete remission in adults 30 years old or younger, and in children with very high-risk disease lacking a sibling donor. Alternative donor stem cell transplantation is an option in high-risk patients without a matched donor who urgently need transplantation. Patients aged less than 60 years, who either are not candidate for allogeneic stem cell transplantation or lack a donor, are candidates for autologous stem cell transplantation. We describe the results of a systematic literature review and an explicit approach to consensus techniques, which resulted in recommendations for the management of primary non-APL acute myeloid leukemia.
由于目前有多种治疗初发急性髓系白血病患者的方法,意大利血液学会及两个附属学会(SIES和GITMO)委托一个专家小组开展项目,旨在制定急性髓系白血病治疗的临床实践指南。在进行系统全面的文献综述后,专家小组针对原发性急性髓系白血病(急性早幼粒细胞白血病除外)的管理制定了建议,并根据支持证据对这些建议进行了分级。当缺乏证据时,添加了基于共识的声明。所有符合强化治疗条件的新诊断患者的一线治疗应包括一个周期的标准剂量阿糖胞苷和蒽环类药物诱导治疗。达到完全缓解后,年龄小于60岁的患者应接受包括大剂量阿糖胞苷的巩固治疗。应在首次完全缓解时进行来自HLA匹配同胞的清髓性异基因干细胞移植:1)细胞遗传学为中高危的儿童或在第二疗程后达到首次完全缓解的儿童;2)年龄小于40岁、中危的成人;年龄小于55岁、细胞遗传学高危或在第二疗程后达到首次完全缓解的成人。对于30岁及以下的成人以及缺乏同胞供体的极高危疾病儿童,建议在首次完全缓解时进行无关供体干细胞移植。对于急需移植但没有匹配供体的高危患者,替代供体干细胞移植是一种选择。年龄小于60岁、不适合进行异基因干细胞移植或缺乏供体的患者是自体干细胞移植的候选者。我们描述了系统文献综述的结果以及达成共识技术的明确方法,这些结果形成了原发性非APL急性髓系白血病管理的建议。