Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Cancer Med. 2019 Sep;8(11):5108-5115. doi: 10.1002/cam4.2418. Epub 2019 Jul 19.
In acute myeloid leukemia (AML), myelodysplasia-related changes contribute to a poor prognosis. This retrospective, propensity score-matched study analyzed 108 newly diagnosed AML patients with features of myelodysplasia syndrome (MDS) (aged 14-60 years) from 2014 to 2018, who received either idarubicin and cytarabine (IA) or decitabine, idarubicin and cytarabine (DAC+IA), and compared efficacy and toxicity between the two regimens. After propensity score matching, there were 54 patients in each group. The rate of complete remission (CR) was higher in the DAC+IA group than in the IA group (85.2% vs 68.5%, P = .040) after the first course, and toxicities were comparable in both groups. Multivariate analysis indicated that the combination with DAC was independent factor for CR rate after the first induction therapy (OR = 2.978, 95% CI:1.090-8.137, P = .033). Subgroup analysis showed a CR advantage for DAC+IA (vs IA) for patients of intermediate-high risk status according to National Comprehensive Cancer Network prognostic stratification. In conclusion, DAC+IA is therefore offered as a new induction choice for newly diagnosed AML patients with features of MDS, aged <60 years old, especially in intermediate-high risk status.
在急性髓系白血病(AML)中,与骨髓增生异常相关的改变导致预后不良。本回顾性、倾向评分匹配研究分析了 2014 年至 2018 年间 108 例年龄在 14-60 岁之间新诊断为具有骨髓增生异常综合征(MDS)特征的 AML 患者,他们接受了阿糖胞苷和伊达比星(IA)或地西他滨、阿糖胞苷和伊达比星(DAC+IA)治疗,并比较了两种方案的疗效和毒性。在倾向评分匹配后,每组各有 54 例患者。DAC+IA 组的完全缓解(CR)率高于 IA 组(首次疗程后 85.2% vs 68.5%,P=0.040),且两组的毒性相当。多因素分析表明,联合 DAC 是首次诱导治疗后 CR 率的独立因素(OR=2.978,95%CI:1.090-8.137,P=0.033)。亚组分析显示,根据国家综合癌症网络预后分层,对于年龄<60 岁、中高危状态的患者,DAC+IA(vs IA)具有 CR 优势。总之,DAC+IA 为新诊断为具有 MDS 特征的 AML 患者提供了新的诱导选择,年龄<60 岁,尤其是中高危状态的患者。