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[IDA-FLAG(伊达比星、氟达拉滨、大剂量阿糖胞苷和粒细胞集落刺激因子)——治疗儿童和青少年复发性急性髓细胞白血病的有效治疗方案。一项初步研究的初步结果]

[IDA-FLAG (idarubicin, fludarabine, high dosage cytarabine and G-CSF)--an effective therapy regimen in treatment of recurrent acute myelocytic leukemia in children and adolescents. Initial results of a pilot study].

作者信息

Fleischhack G, Graf N, Hasan C, Ackermann M, Breu H, Zernikow B, Bode U

机构信息

Universitätskinderklinik Bonn.

出版信息

Klin Padiatr. 1996 Jul-Aug;208(4):229-35. doi: 10.1055/s-2008-1046478.

Abstract

Intensive chemotherapy has improved the prognosis of patients with AML. The success rate of relapse treatment correlates with the length of first remission. Thus early relapses and primarily refractory diseases have a grave prognosis. New chemotherapeutic regimens could be useful for those patients. Patients treated for newly diagnosed or relapsed AML with polychemotherapy regimen of the AML-BFM-studies containing induction, consolidation and high-dose cytarabine combined with mitoxantrone (HAM) and relapsed within 2 up to 31 months after the first CR entered a pilot trial, the so called IDA-FLAG regimen. This regimen includes G-CSF (day 0 up to ANC > 1000/microliter, 400 micrograms/m2.d), fludarabine (day 1-4, 30 mg/m2.d), high-dose cytarabine (day 1-4, 2000 mg/m2.d) and idarubicin (day 2-4, 12 mg/m2.d). 10 patients aged 1,8 to 28,1 years (mean = 9,6 years) having the first (n = 8) or second relapse (n = 1) of AML or an acute blastcrisis of myelodysplastic syndrome (n = 1) (FAB classification: M1/M2 = 3, M4/M5 = 5, M7 = 1, CMML = 1) received 14 courses. Overall, 7 patients achieved CR with a mean duration of 8,9 months (1-22 months), one patient showed a partial remission and two were nonresponders. 4 patients are in continuous CR for 7,5 to 22 months (mean = 13,2 months). 3 patients got a bone marrow transplantation (allogenic = 2, autologous = 1) in CR following this treatment. Toxicity was considerable, mainly bone marrow aplasia with leucopenia < 1000/microliter for 15 to 40 days (mean = 26,1 days), neutropenia < 500/microliter for 14 to 39 days (mean = 26,0 days) and thrombocytopenia < 30,000/microliter for 14 to 90 days (mean = 36,5 days). Further important side effects were fever, mucositis and pneumonia. One patient died from an fulminant aspergillus sepsis during long-term neutropenia. The sequential administration of G-CSF, fludarabine, cytarabine and idarubicin is effective in treatment of relapsed AML in childhood and an advisable option prior to allogenic or autologous bone marrow transplantation. With regard to the unfavorable prognosis of relapsed or refractory AML the toxicity of this regimen seems acceptable.

摘要

强化化疗改善了急性髓系白血病(AML)患者的预后。复发治疗的成功率与首次缓解期的长短相关。因此,早期复发和原发性难治性疾病的预后较差。新的化疗方案可能对这些患者有用。接受包含诱导、巩固和大剂量阿糖胞苷联合米托蒽醌(HAM)的AML - BFM研究多药化疗方案治疗新诊断或复发AML的患者,在首次完全缓解(CR)后2至31个月内复发,进入了一项试点试验,即所谓的IDA - FLAG方案。该方案包括粒细胞集落刺激因子(第0天至中性粒细胞绝对计数>1000/微升,400微克/平方米·天)、氟达拉滨(第1 - 4天,30毫克/平方米·天)、大剂量阿糖胞苷(第1 - 4天,2000毫克/平方米·天)和伊达比星(第2 - 4天,12毫克/平方米·天)。10例年龄在1.8至28.1岁(平均 = 9.6岁)的患者,患有AML的首次(n = 8)或第二次复发(n = 1)或骨髓增生异常综合征的急性原始细胞危象(n = 1)(FAB分类:M1/M2 = 3例,M4/M5 = 5例,M7 = 1例,慢性粒 - 单核细胞白血病 = 1例)接受了14个疗程的治疗。总体而言,7例患者达到CR,平均持续时间为8.9个月(1 - 22个月),1例患者显示部分缓解,2例无反应。4例患者持续CR 7.5至22个月(平均 = 13.2个月)。3例患者在该治疗后的CR期接受了骨髓移植(异基因 = 2例,自体 = 1例)

毒性相当大,主要是骨髓再生障碍,白细胞减少<1000/微升持续15至40天(平均 = 26.1天),中性粒细胞减少<500/微升持续十四至39天(平均 = 26.0天),血小板减少<30,000/微升持续14至90天(平均 = 36.5天)。其他重要的副作用是发热、黏膜炎和肺炎。1例患者在长期中性粒细胞减少期间死于暴发性曲霉菌败血症

粒细胞集落刺激因子、氟达拉滨、阿糖胞苷和伊达比星的序贯给药对儿童复发AML的治疗有效,并且是异基因或自体骨髓移植之前的一个可取选择。鉴于复发或难治性AML的预后不良,该方案的毒性似乎是可以接受的。

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