Service d'hématologie clinique, Hôpital d'Instruction des Armées Percy, 101 Av Henri Barbusse, 92141 Clamart, France.
Ann Hematol. 2012 Dec;91(12):1871-7. doi: 10.1007/s00277-012-1528-9. Epub 2012 Jul 21.
Current salvage therapies for relapsed acute myeloid leukemia (AML) are unsatisfactory. We retrospectively evaluated the efficacy and toxicity of fractionated doses of gemtuzumab ozogamicin (GO) combined with a standard 3 + 7 induction regimen in young patients with AML in first relapse. Salvage regimen consisted of GO 3 mg/m² on days 1, 4, and 7; cytarabine, 200 mg/m² on days 1-7; and daunorubicine, 60 mg/m²; or idarubicine, 12 mg/m² on days 1-3. Fourteen patients were treated between April 2008 and April 2011. Median age was 46 years (29-58), median white blood cell count is 3.4 10⁹/L (0.9-19), and median first complete remission (CR) duration is 11 months (1-42). All the patients had previously received high or intermediate doses of cytarabine as consolidation therapy. Salvage treatment was performed as scheduled for the 14 patients, using daunorubicine in 12 patients and idarubicine in two. Overall response rate was 79 % with six CR and five CR with incomplete platelet recovery. Median times to neutrophil (>0.5 10⁹/L) and platelet (>20 10⁹/L) recovery were 29 days (23-32) and 36 days (28-48), respectively. Allogeneic transplantation was performed in the 11 responding patients within a median time of 4 months (3-10). Three mild and one moderate veno-occlusive disease (VOD) occurred after salvage and two moderate VOD after transplantation. Median and 2-year overall survival (OS) were 10 months and 42 %, respectively. For responders, estimated 2-year OS was 53 % (median OS not reached). This salvage regimen seems safe and effective in younger patients with AML in first relapse allowing allogeneic transplantation in CR2 for most patients.
目前,复发急性髓系白血病(AML)的挽救性治疗效果并不理想。我们回顾性评估了小剂量分次给予吉妥珠单抗奥佐米星(GO)联合标准 3+7 诱导方案治疗首次复发的年轻 AML 患者的疗效和毒性。挽救性方案包括 GO 3mg/m²,第 1、4 和 7 天;阿糖胞苷 200mg/m²,第 1-7 天;柔红霉素 60mg/m²或伊达比星 12mg/m²,第 1-3 天。2008 年 4 月至 2011 年 4 月期间,共有 14 例患者接受了治疗。中位年龄为 46 岁(29-58 岁),中位白细胞计数为 3.4×10⁹/L(0.9-19),中位首次完全缓解(CR)时间为 11 个月(1-42 个月)。所有患者先前均接受高剂量或中剂量阿糖胞苷作为巩固治疗。14 例患者均按计划接受挽救性治疗,其中 12 例使用柔红霉素,2 例使用伊达比星。总缓解率为 79%,其中 6 例为完全缓解,5 例为不完全血小板恢复的完全缓解。中性粒细胞(>0.5×10⁹/L)和血小板(>20×10⁹/L)恢复的中位时间分别为 29 天(23-32 天)和 36 天(28-48 天)。11 例有反应的患者在中位时间 4 个月(3-10 个月)内进行了异基因移植。挽救治疗后发生 3 例轻度和 1 例中度静脉阻塞性疾病(VOD),移植后发生 2 例中度 VOD。中位和 2 年总生存率(OS)分别为 10 个月和 42%。对于有反应的患者,估计 2 年 OS 为 53%(中位 OS 未达到)。该挽救性方案在首次复发的年轻 AML 患者中似乎是安全有效的,可使大多数患者在 CR2 时进行异基因移植。