Cahn J Y, Labopin M, Sierra J, Blaise D, Reiffers J, Ferrant A, Bergmann L, Visani G, Cornelissen J, De Witte T, Bosi A, Frassoni F, Gorin N C
Haematology Department, Hôpital Jean Minjoz, Besançon, France.
Br J Haematol. 2000 Aug;110(2):308-14. doi: 10.1046/j.1365-2141.2000.02178.x.
High-dose cytarabine is currently used in combination with anthracycline in the treatment of acute myeloblastic leukaemia (AML). Moreover, high-dose cytarabine has been reported to produce long-term disease-free survival in a proportion of patients, especially in certain subtypes of AML. However, it remains unknown whether the outcome of patients undergoing allogeneic or autologous stem cell transplantation is influenced by previous treatment with high-dose cytarabine. To this end, 1672 patients with AML in first remission who were reported to the Acute Leukaemia Working Party registry of the European Group for Blood and Marrow Transplantation (EBMT) and who were transplanted between 1980 and 1995 were analysed according to the dose intensity of cytarabine given at induction and/or consolidation. Autologous stem cell transplantation (ABMT) was performed in 846 patients and allogeneic bone marrow transplantation (BMT) in 826 patients. This study shows that the dose of cytarabine (Ara-C) given at induction and/or consolidation did not influence the relapse incidence in patients subsequently allografted or autografted. In addition, it did not give any advantage in terms of overall outcome. Therefore, high-dose (HD) Ara-C may not be needed for patients who have a planned stem cell transplantation (SCT) as post-remission therapy. Nevertheless, HD Ara-C may be utilized in certain subtypes of AML that are believed to be curable by chemotherapy alone.
大剂量阿糖胞苷目前与蒽环类药物联合用于治疗急性髓细胞白血病(AML)。此外,据报道大剂量阿糖胞苷能使一部分患者实现长期无病生存,尤其是某些AML亚型患者。然而,接受异基因或自体干细胞移植的患者的预后是否受先前大剂量阿糖胞苷治疗的影响仍不清楚。为此,对1980年至1995年间向欧洲血液和骨髓移植组(EBMT)急性白血病工作组登记处报告且处于首次缓解期的1672例AML患者,根据诱导和/或巩固治疗时给予的阿糖胞苷剂量强度进行了分析。846例患者接受了自体干细胞移植(ABMT),826例患者接受了异基因骨髓移植(BMT)。本研究表明,诱导和/或巩固治疗时给予的阿糖胞苷(Ara-C)剂量不影响随后接受异基因移植或自体移植患者的复发率。此外,就总体预后而言,它没有带来任何优势。因此,对于计划进行干细胞移植(SCT)作为缓解后治疗的患者,可能不需要大剂量(HD)Ara-C。然而,HD Ara-C可用于某些据信仅通过化疗就能治愈的AML亚型。