机构地区:[1]中山大学附属第一医院血液科,广东广州510080 [2]广东省人民医院血液科,广东广州510080
出 处:《癌症》2004年第4期430-434,共5页Chinese Journal of Cancer
摘 要:背景与目的:三氧化二砷(arsenictrioxide,As2O3)治疗急性早幼粒细胞白血病作用机制与全反式维甲酸(all-transretinonicacid,ATRA)有所不同,前者主要是加速细胞的凋亡,后者是诱导细胞的分化。但两者均能抑制急性早幼粒细胞白血病组织因子(tissuefactor,TF)mRNA的转录,降低TF水平和促凝活性,从而改善患者的出凝血异常。本研究旨在探讨两药联合应用能否提高疗效及是否加重不良反应。方法:采用历史对照分组。2000年1月~2001年10月的22例急性早幼粒细胞白血病作为ATRA组,其中初治17例,复发5例;单用ATRA治疗,剂量为25mg/(m2·d),分两次口服,一个疗程最长不超过50天。2001年11月~2003年6月的急性早幼粒细胞白血病19例为联合治疗组,其中初治15例,复发4例,采用As2O3与ATRA联合治疗。治疗剂量为0.1%As2O3溶液10ml,加入5%葡萄糖溶液中静脉滴注,每天1次,持续4~6h,28天为一疗程,ATRA的剂量用法同前组。结果:ATRA治疗组22例中19例(初治16例,复发3例)获完全缓解,完全缓解率为86.4%。联合治疗组19例中17例(初治15例,复发2例)获完全缓解,缓解率为89.5%。病死率ATRA组为18.6%,共3例(1例初治,2例复发);联合治疗组为10.5%,共2例(均为复发者)。完全缓解率和病死率两组比较无统计学差异(P>0.05)。达到完全缓解的中位时间。BACKGROUND & OBJECTIVE: The mechanism of effect of arsenic t ri oxide on promyelocytic leukemia is different from that of all- trans retinoic a cid. Arsenic trioxide exerts its action by accelerating cell apoptosis, while al l- trans retinoic acid by inducing cell differentiation. However, both drugs ca n inhibit the transcription of tissue factor (TF) mRNA in acute promyelocytic le ukemia, and decrease TF level and coagulative activity to normalize coagulopathy . The objective of the study was to observe whether combination of the two drugs could improve efficacy or in contrary accentuate adverse reactions. METHODS: Tw o groups of patients with acute promyelocytic leukemia were included. Twenty- t wo patients (17 untreated cases and 5 relapsed cases) from January 2000 to Octob er 2001 in group Ⅰ were treated only with oral retinoic acid [25 mg/(m2· d) i n two divided doses] for less than 50 days. Ninteen cases (15 untreated cases an d 4 relapsed cases) from November 2001 to June 2003) in Group Ⅱ were treated w ith combination of arsenic trioxide and all- trans retinoic acid. 0.1% AS2O3 10 ml in 500 ml 5% glucose solution was given intravenously for 4 to 6 hours p er day for 28 days. The dosage of retinoic acid in group Ⅱ was the same as tha t in group Ⅰ . RESULTS: Nineteen of 22 cases in retinoic acid- treated group ( group Ⅰ )(16 untreated cases and 3 relapsed cases) achieved complete remission (CR). The CR rate was 86.4% . Seventeen of 19 cases in combination therapy grou p (group Ⅱ )(15 untreated cases and 2 relapsed cases) achieved CR. The CR rate was 89.5% . The death rates were 13.6% (3/22, 1 untreated case, 2 relapsed ca ses) in group Ⅰ and 10.5% (2/19, 2 relapsed cases) in group Ⅱ , respectivel y. The median time to CR was 23 days in group Ⅰ and 26 days in group Ⅱ , and the median time to normalization of coagulopathy was 7 days in group Ⅰ and 4 d ays in group Ⅱ . Significant differences were found between the two groups. No significant adverse reaction was obser
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