Hématologie Adulte, Hôpital Saint-Louis, APHP, Université Paris Diderot, 1 Avenue Claude Vellefaux 75010, Paris, France.
Department of Oncology, Division of Haematology, AOU Città Della Salute E Della Scienza Di Torino, Turin, Italy.
Ann Hematol. 2023 Apr;102(4):761-768. doi: 10.1007/s00277-023-05119-3. Epub 2023 Feb 11.
Hyperleukocytosis is associated with a significant early mortality rate in patients with acute myeloid leukemia (AML). To date, no controlled trial has ever evaluated a strategy to reduce this risk, and the initial management of these patients remains heterogeneous worldwide. The aim of the present study was to evaluate the influence of a short course of intravenous dexamethasone on the early outcomes of patients with hyperleukocytic AML with white blood cell (WBC) count above 50 × 10/L. Clinical and biological data of all consecutive patients (1997-2017) eligible for intensive chemotherapy from a single center were retrospectively collected. A total of 251 patients with a median age of 51 years and a median WBC count of 120 × 10/L were included, 95 of whom received dexamethasone. Patients treated with dexamethasone had higher WBC count and a more severe disease compared with those who did not, and they presented more often with leukostasis and hypoxemia, resulting in a more frequent need for life-sustaining therapies (p < 0.001). To account for these imbalances, patients were compared after adjusting for a propensity score, which included all variables with a prognostic influence in the overall cohort. In the matched cohort, dexamethasone was associated with lower early death (OR = 0.34, p = 0.0026) and induction failure rate (OR = 0.44, p = 0.02) and better overall survival (HR = 0.60, p = 0.011), with no impact on relapse risk (cHR = 0.73, p = 0.39). The overall survival benefit was confirmed among all tested subgroups. This study suggests that dexamethasone administration is safe and associated with a lower risk of induction mortality in patients with hyperleukocytic AML and deserves prospective evaluation.
高白细胞血症与急性髓系白血病(AML)患者的早期死亡率显著相关。迄今为止,尚无对照试验评估降低这种风险的策略,这些患者的初始治疗在全球范围内仍然存在差异。本研究旨在评估短期静脉内地塞米松治疗白细胞计数高于 50×10/L 的高白细胞性 AML 患者的早期结局的影响。回顾性收集了来自单一中心的所有符合强化化疗条件的连续患者(1997-2017 年)的临床和生物学数据。共纳入 251 例中位年龄为 51 岁、中位白细胞计数为 120×10/L 的患者,其中 95 例接受地塞米松治疗。与未接受地塞米松治疗的患者相比,接受地塞米松治疗的患者白细胞计数更高,疾病更严重,更常出现白细胞淤滞和低氧血症,因此更需要维持生命的治疗(p<0.001)。为了弥补这些不平衡,在调整了对整个队列有预后影响的所有变量的倾向评分后,对患者进行了比较。在匹配队列中,地塞米松与早期死亡率降低(OR=0.34,p=0.0026)和诱导失败率降低(OR=0.44,p=0.02)相关,总生存率更好(HR=0.60,p=0.011),但对复发风险无影响(cHR=0.73,p=0.39)。在所有测试的亚组中均证实了总生存率的获益。本研究表明,地塞米松的应用是安全的,并可降低高白细胞性 AML 患者诱导死亡率的风险,值得进一步前瞻性评估。