Section of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Turin, via Genova, 3, 10126, Turin, Italy,
Ann Hematol. 2014 Aug;93(8):1391-400. doi: 10.1007/s00277-014-2047-7. Epub 2014 Apr 6.
We evaluated a maintenance, post-remission treatment with low-dose chemotherapy plus differentiating agents on poor-prognosis acute myeloid leukemia (AML)/myelodysplastic syndrome (MDS) patients ineligible to allografting. Patients had either age over 60 and/or secondary AML, therapy-related AML, previous relapse, high-risk MDS. Forty-five patients received the maintenance therapy based on two alternated schedules: (a) 6-thioguanine + 13-cis retinoic acid + dihydroxylated vitamin D3 and (b) low-dose cytarabine + 6-mercaptopurine + all-trans retinoic acid + dihydroxylated vitamin D3. We compared their outcome, at a median follow-up of 52 months, to that of a matched population of 49 patients who stopped treatments after consolidation. Maintenance group had a lower relapse incidence (70.3 vs. 86.4 % at 5 years p = 0.007) and a longer disease-free survival (median 21.2 vs. 8.7 months, p = 0.017). The relapse reduction improved overall survival: median 40.4 months (35.9 % at 5 years) for maintenance group vs. 15.8 (14.2 % at 5 years) for controls (p = 0.005). At multivariate Cox analysis, both cytogenetic and maintenance therapies resulted independent outcome predictors for overall survival. Maintenance treatment also reduced minimal residual disease (detected by WT1 and CBFβ-MYH11) in five of eight evaluable patients. The present results suggest that our strategy of maintenance therapy might improve the outcome of poor-risk AML/MDS patients.
我们评估了低剂量化疗联合分化诱导剂维持治疗对不适合移植的预后不良的急性髓细胞白血病(AML)/骨髓增生异常综合征(MDS)患者的疗效。患者具有以下特征:年龄>60 岁和/或继发性 AML、治疗相关 AML、既往复发、高危 MDS。45 例患者接受了基于两种交替方案的维持治疗:(a)6-硫鸟嘌呤+13-顺式维甲酸+二羟维生素 D3 和(b)低剂量阿糖胞苷+6-巯基嘌呤+全反式维甲酸+二羟维生素 D3。我们比较了这些患者的结果,中位随访时间为 52 个月,并与 49 例巩固治疗后停止治疗的匹配患者的结果进行了比较。维持组的复发率较低(5 年时为 70.3% vs. 86.4%,p=0.007),无疾病生存时间较长(中位时间为 21.2 个月 vs. 8.7 个月,p=0.017)。复发减少改善了总生存:维持组的中位总生存时间为 40.4 个月(5 年时为 35.9%),而对照组为 15.8 个月(5 年时为 14.2%)(p=0.005)。多变量 Cox 分析显示,细胞遗传学和维持治疗均为总生存的独立预后预测因素。维持治疗还使 8 例可评估患者中的 5 例微小残留病(通过 WT1 和 CBFβ-MYH11 检测)减少。这些结果表明,我们的维持治疗策略可能改善高危 AML/MDS 患者的预后。