Hematology, Department of Precision and Translational Medicine, Azienda Ospedaliera Policlinico Umberto I, Sapienza University, Via Benevento 6, 00161, Rome, Italy.
Department of Statistical Sciences, Sapienza University, Rome, Italy.
Ann Hematol. 2019 Aug;98(8):1919-1925. doi: 10.1007/s00277-019-03724-9. Epub 2019 Jun 5.
The outcome of high-risk myelodysplastic syndrome (MDS) patients treated with 5-azacitidine (5-AZA) in the real-life setting remains largely unknown. We evaluated 110 MDS patients (IPSS intermediate 2/high) treated outside of clinical trials at a single institution between September 2003 and January 2017. Median duration of therapy was 9.5 cycles. The overall survival (OS) of the whole cohort was 66.1% at 1 year and 38.3% at 2 years. No differences in terms of OS were observed with regard to gender (p = 0.622) and age at baseline (< 65 years, 65-75, and > 75 years, p = 0.075). According to the IPSS-R, the very high-risk group had an inferior 2-year OS (17%) compared with intermediate-group patients (64%, p < 0.001). Transfusion independency at baseline was identified as a favorable prognostic factor on 1-year (66.8%) and 2-year OS (43.4%) (p < 0.001). After four cycles, the persistence of bone marrow blasts > 10% identified patients with a worse outcome, with a 2-year OS of 9.4% (p = 0.002). The occurrence of an infection during the first four cycles impacted on the 2-year OS (31.6% vs 58.3% in patients without infections, p = 0.032). Patients receiving at least 24 cycles of the drug have a 5-year OS of 38.2%. This analysis allowed to identify features at baseline or during treatment with 5-AZA associated with a different 2-year OS.
在真实环境中,接受 5-氮杂胞苷(5-AZA)治疗的高危骨髓增生异常综合征(MDS)患者的结局在很大程度上仍不清楚。我们评估了 2003 年 9 月至 2017 年 1 月期间在一家机构接受临床试验以外的 5-AZA 治疗的 110 例 MDS 患者(国际预后评分系统(IPSS)中危 2/高危)。中位治疗持续时间为 9.5 个周期。整个队列的总生存期(OS)在 1 年时为 66.1%,在 2 年时为 38.3%。在性别(p=0.622)和基线时的年龄(<65 岁、65-75 岁和>75 岁,p=0.075)方面,OS 无差异。根据 IPSS-R,极高危组的 2 年 OS(17%)低于中危组(64%,p<0.001)。基线时的输血独立性被确定为 1 年(66.8%)和 2 年 OS(43.4%)的有利预后因素(p<0.001)。在四个周期后,骨髓原始细胞>10%的持续存在确定了预后较差的患者,其 2 年 OS 为 9.4%(p=0.002)。在头四个周期中发生感染会影响 2 年 OS(无感染患者为 31.6%,感染患者为 58.3%,p=0.032)。接受至少 24 个周期药物治疗的患者 5 年 OS 为 38.2%。这项分析确定了基线或接受 5-AZA 治疗期间与不同 2 年 OS 相关的特征。