Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.
Department of Public Health, Wrocław Medical University, Wrocław, Poland.
Hematology. 2021 Dec;26(1):556-564. doi: 10.1080/16078454.2021.1956182.
Azacitidine (AZA) is the standard of care for higher-risk myelodysplastic syndrome (HR-MDS) patients ineligible for intensive therapy. Clinical outcome discrepancies reported in clinical trials and real-life settings stimulate the search for new prognostic factors.
We retrospectively evaluated 315 MDS, 20-30% blast acute myeloid leukemia (AML) and chronic myelomonocytic leukemia (CMML) patients treated with azacitidine in 12 centers cooperating within the Polish Adult Leukemia Group (PALG).
The median number of AZA cycles was 7 (1-69) and 24% patients received fewer than 4 cycles (early failure, EF). Serum albumin level was an independent predictor of EF occurrence. Complete remission (CR) was obtained in 20% and partial remission (PR) in 12% of patients. Hematologic improvement - erythroid (HI-E), neutrophil (HI-N), or platelet (HI-P) was achieved in 51%, 36%, and 48% of patients, respectively. No factors significantly predicted CR or PR in the multivariate analysis. For HI-E and HI-P, lower LDH level predicted response. Median survival was 15 (13-19) months. Lower serum albumin level, serious infection and receiving <4 AZA cycles independently predicted a worse overall survival (OS) ( < 0.05).
Serum albumin assessment before azacitidine treatment can help to identify patients with higher risk of early failure and worse clinical outcome.
阿扎胞苷(AZA)是不适合强化治疗的高危骨髓增生异常综合征(HR-MDS)患者的标准治疗方法。临床试验和实际治疗环境中报告的临床结果差异促使人们寻找新的预后因素。
我们回顾性评估了 12 个波兰成人白血病组(PALG)合作中心的 315 例 MDS、20-30%原始细胞急性髓系白血病(AML)和慢性髓单核细胞白血病(CMML)患者,这些患者接受了 AZA 治疗。
AZA 周期的中位数为 7(1-69),24%的患者接受的周期少于 4 个(早期失败,EF)。血清白蛋白水平是 EF 发生的独立预测因子。20%的患者获得完全缓解(CR),12%的患者获得部分缓解(PR)。分别有 51%、36%和 48%的患者出现血液学改善-红细胞(HI-E)、中性粒细胞(HI-N)或血小板(HI-P)。多变量分析未发现 CR 或 PR 的显著预测因素。对于 HI-E 和 HI-P,较低的 LDH 水平预测有反应。中位生存时间为 15(13-19)个月。较低的血清白蛋白水平、严重感染和接受<4 个 AZA 周期独立预测总生存期(OS)更差(<0.05)。
在接受 AZA 治疗之前评估血清白蛋白水平可以帮助识别早期失败风险较高和临床结局较差的患者。