Wang Fang, Jia Jin-Song, Wang Jing, Zhao Ting, Jiang Qian, Jiang Hao, Zhu Hong-Hu
Peking University People's Hospital, Peking University Institute of Hematology, Beijing 100044, China; Peking University International Hospital, Department of Hematology, Beijing, 102206, China.
Peking University People's Hospital, Peking University Institute of Hematology, Beijing 100044, China.
Leuk Res. 2017 Oct;61:84-88. doi: 10.1016/j.leukres.2017.09.006. Epub 2017 Sep 14.
We aimed to compare the kinetics of white blood cell (WBC) and explore predictive factors of leukocytosis in non-high-risk acute promyelocytic leukemia (APL), with oral arsenic plus all-trans retinoic acid (ATRA) or intravenous arsenic trioxide (ATO) plus ATRA as a first-line treatment.
The absolute count, doubling time and peak time of WBC were analyzed in 64 newly diagnosed non-high-risk APL patients who were treated with different induction regimens containing either oral Realgar-indigo naturalis formula (RIF) (n=35) or ATO (n=29). The end points were the dynamic changes of the WBC counts during induction. The time points started at day 1 and were selected over 3-day intervals for 28days.
Among the 64 included patients, the median initial and peak WBC counts were 1.78×10/L (range 0.31-9.89) and 12.16×10/L (range 1.56-80.01), respectively. The incidence of differentiation syndrome was 9.38%. The dynamic changes in leukocytosis showed a single peak wave in all the patients, and the median time to peak was 10 (range 2-26) days. A higher WBC count was observed in the RIF group than in the ATO group after 10days of treatment (9.22×10/L vs. 4.10×10/L, p=0.015). Patients with the peak WBC count >10×10/L had a shorter WBC doubling time compared to patients with a lower peak WBC (RIF group 4days vs. 7days, p=0.001; ATO group 4.5days vs. 23days, p=0.002). Univariate and multivariable analyses showed that the doubling time of WBC is an independent factor for the peak WBC count.
Different kinetics of WBC proliferation were observed during induction with oral arsenic plus ATRA and ATO plus ATRA. The doubling time of WBC is an important independent factor for predicting the peak WBC count.
我们旨在比较非高危急性早幼粒细胞白血病(APL)患者接受口服砷剂联合全反式维甲酸(ATRA)或静脉注射三氧化二砷(ATO)联合ATRA作为一线治疗时白细胞(WBC)的动力学变化,并探讨白细胞增多症的预测因素。
分析了64例新诊断的非高危APL患者的WBC绝对计数、倍增时间和峰值时间,这些患者接受了含口服雄黄-青黛方(RIF)(n = 35)或ATO(n = 29)的不同诱导方案治疗。终点为诱导期间WBC计数的动态变化。时间点从第1天开始,每3天选取一次,共28天。
在纳入的64例患者中,初始WBC计数中位数和峰值分别为1.78×10⁹/L(范围0.31 - 9.89)和12.16×10⁹/L(范围1.56 - 80.01)。分化综合征的发生率为9.38%。所有患者白细胞增多症的动态变化均显示为单峰波,峰值出现的中位时间为10天(范围2 - 26天)。治疗10天后,RIF组的WBC计数高于ATO组(9.22×10⁹/L对4.10×10⁹/L,p = 0.015)。与峰值WBC较低的患者相比,峰值WBC计数>10×10⁹/L的患者WBC倍增时间更短(RIF组4天对7天,p = 0.001;ATO组4.5天对23天,p = 0.002)。单因素和多因素分析表明,WBC倍增时间是预测峰值WBC计数的独立因素。
口服砷剂联合ATRA和ATO联合ATRA诱导治疗期间观察到不同的WBC增殖动力学变化。WBC倍增时间是预测峰值WBC计数的重要独立因素。