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作 者:张新华[1] 冉启杰[1] 周敏[1] 李菁媛[1] 王军[1] 徐彪[1] 宋森花[1] 马梅凌[1] 龚静[1] 刘龙龙[1] 谢红[1] 罗晓静[1]
出 处:《内科急危重症杂志》2014年第3期170-172,共3页Journal of Critical Care In Internal Medicine
摘 要:目的:观察改良CHG方案治疗初诊成人高白细胞性急性髓系白血病(HAML)的疗效及不良反应。方法:23例初诊成人HAML患者接受改良CHG方案化疗:高三尖杉酯碱(HHT)2mg/d,静脉滴注;阿糖胞苷(Ara—C)10mg/(m^2·d),皮下注射,1次/12h,共14d,化疗过程中,WBC〈10×10^9/L时予粒细胞集落刺激因子(G—CSF)300μg/d,皮下注射,直至中性粒细胞绝对值(ANC)≥1.5×10^9/L时停用。结果:15例(65.2%)获得完全缓解(CR),2例(8.7%)部分缓解(PR),总有效率(OR)73.9%。早期死亡2例,病死率8.7%。WBC计数降至10×10^9/L以下所需时间为6(4—10)d。化疗期间主要不良反应为骨髓抑制,表现为粒细胞缺乏及继发感染、出血。结论:改良CHG方案治疗初诊成人高白细胞性急性髓系白血病有效率高,不良反应可控制。Objective: To observe the efficacy and side effect of modified CHG regimen [ ( homoharringtonine ( HHT), cytosine arabinoside (Ara-C) and grannlocyte colony stimulating factor(G-CSF) ] for treatment of the newly diagnosed adult patients with hyperleukocytic acute myeloid leukemia (HAML). Methods: Twenty-three adult patients with HAML were treated with modified CHG regimen: HHT 2 mg/d intravenously; Ara-C 10mg/( m2 · d) hypodermically once 12 hours for 14 days; and G-CSF 300 μg/d hypodermically when WBC 〈 10 ×10^9/L until absolute nentrophil count (ANC) ≥ 1.5×10^9/L. Results: Fifteen cases (65.2%) achieved complete remission (CR), 2 cases (8.7%) partial remission (PR), the overall response rate (OR) was 73.9%. Two of them died and the early mortality was 8.7%. The WBC counts decreased below 10 ×10^9/L necessitated 6 (4 - 10) days of modified CHG treatments. The main adverse effect during the chemotherapy was myelosuppression, manifested as neutropenia with secondary infection and bleeding. Conclusions: The efficacy of modified CHG regimen for newly diagnosed adult patients with HAML is rather high and the side effects are controllable.
关 键 词:急性髓系白血病 高白细胞性 高三尖杉酯碱 阿糖胞苷 粒细胞集落刺激因子
分 类 号:R552[医药卫生—血液循环系统疾病]
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