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首页> 外文期刊>European Journal of Haematology >Long-term prognosis of childhood acute promyelocytic leukaemia with arsenic trioxide administration in induction and consolidation chemotherapy phases: A single-centre experience
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Long-term prognosis of childhood acute promyelocytic leukaemia with arsenic trioxide administration in induction and consolidation chemotherapy phases: A single-centre experience

机译:三氧化二砷在诱导和巩固化疗阶段对儿童急性早幼粒细胞白血病的长期预后:单中心经验

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摘要

Objectives: The efficacy of all-trans retinoic acid (ATRA) and arsenic trioxide (As2O3) as induction therapy for adult acute promyelocytic leukaemia (APL) has been documented in several clinical trials. However, the role of ATRA/As2O3 combination in induction and consolidation therapy in children remains unclear. Here, we report the efficacy of combined treatment with As2O3 and ATRA as induction and consolidation chemotherapy to treat newly diagnosed childhood APL. Methods: From 1998 to 2011, 43 children with newly diagnosed APL received induction and consolidation chemotherapy with ATRA and As2O3 (Protocol B). Rates of complete remission (CR), event-free survival (EFS), disease-free survival (DFS), and overall survival (OS) and drug toxicity were compared between children treated with Protocol B and 25 others treated previously with ATRA alone as induction chemotherapy (Protocol A). Results: Of 43 patients treated with Protocol B, 41 (95.4%) achieved CR (two died of intracranial haemorrhage on day 10 and 14). In contrast, only 20 (80%) of 25 patients treated with Protocol A achieved CR. Thus, the CR rate was significantly lower in patients receiving induction chemotherapy with Protocol A than in those treated with Protocol B (P = 0.045, χ2 = 6.508). Of the 41 patients who achieved CR on induction therapy with Protocol B, 40 also received consolidation therapy. Molecular relapse, but no overt morphological relapse, occurred in one patient at 25 months after diagnosis; this patient regained CR status with As2O3 treatment. With a median follow-up period of 75 months, estimated EFS, DFS and OS rates were 92.5 ± 4.2%, 97.1 ± 2.9% and 95.3 ± 3.2%, respectively, for Protocol B. In contrast, with a median follow-up of 127 months, the EFS, DFS and OS rates at 75 months were 70.4 ± 9.4%, 76.4 ± 9.2% and 70.4 ± 9.4%, respectively, for Protocol A. Thus, patients treated with Protocol A showed significantly lower EFS (P = 0.021) and OS (P = 0.007) rates than those treated with Protocol B. Conclusions: Application of As2O3 and ATRA as induction and consolidation chemotherapy resulted in excellent outcomes and improved long-term prognosis in children with newly diagnosed APL.
机译:目的:全反式维甲酸(ATRA)和三氧化二砷(As2O3)作为成人急性早幼粒细胞白血病(APL)诱导疗法的疗效已得到证实。但是,尚不清楚ATRA / As2O3组合在儿童诱导和巩固治疗中的作用。在这里,我们报告与As2O3和ATRA联合治疗作为诱导和巩固化疗治疗新诊断的儿童APL的功效。方法:1998年至2011年,对43例新诊断为APL的儿童进行了ATRA和As2O3(方案B)的诱导和巩固化疗。比较接受方案B治疗的儿童与之前接受单独ATRA治疗的其他25名儿童的完全缓解率(CR),无事件生存率(EFS),无病生存率(DFS),总生存率(OS)和药物毒性。诱导化疗(方案A)。结果:在接受B方案治疗的43例患者中,有41例(95.4%)达到了CR(2例在第10和14天死于颅内出血)。相反,接受方案A治疗的25例患者中只有20例(80%)达到了CR。因此,接受方案A诱导化疗的患者的CR率显着低于方案B治疗的患者(P = 0.045,χ2= 6.508)。在通过方案B的诱导疗法获得CR的41例患者中,有40例也接受了巩固治疗。诊断后25个月,一名患者发生了分子复发,但没有明显的形态学复发。该患者通过As2O3治疗恢复了CR状态。协议B的中位随访期为75个月,估计的EFS,DFS和OS发生率分别为92.5±4.2%,97.1±2.9%和95.3±3.2%。 127个月,方案A的75个月EFS,DFS和OS发生率分别为70.4±9.4%,76.4±9.2%和70.4±9.4%。因此,接受方案A治疗的患者的EFS显着降低(P = 0.021 )和OS(P = 0.007)的发生率均高于用方案B进行治疗的患者。结论:As2O3和ATRA作为诱导和巩固化疗的应用在新诊断为APL的儿童中获得了优异的疗效并改善了长期预后。

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