Tavil Betul, Aytac Selin, Balci Yasemin Isik, Unal Sule, Kuskonmaz Barıs, Yetgin Sevgi, Gurgey Aytemiz, Tuncer Murat, Gumruk Fatma, Uckan Duygu, Cetin Mualla
Pediatric Hematology Unit, Ihsan Dogramacı Children's Hospital, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Pediatr Hematol Oncol. 2010 Oct;27(7):517-28. doi: 10.3109/08880018.2010.493578.
Fludarabine, cytarabine, granulocyte colony-stimulating factor (G-CSF), and idarubicin (FLAG-IDA) regimen has been proven to be a potentially useful chemotherapy regimen for relapsed or poor-prognosis childhood leukemia. The aim of the study was to evaluate complete remission (CR) rate, toxicity, and overall survival of children with poor-prognosis acute leukemia who received the FLAG-IDA regimen. Furthermore, the authors investigated the children who achieved CR following FLAG-IDA treatment regarding their eligibility for allogeneic hematopoietic stem cell transplantation (HSCT). Between January 2002 and April 2007, 25 children with poor-prognosis acute leukemia were treated with FLAG-IDA regimen in our center. Of the 25 children (16 AML, 9 ALL) with poor-prognosis acute leukemia, 7 (28.0%) received 1 cycle, 17 (68.0%) received 2 cycles, and 1 (4%) received 3 cycles of FLAG or FLAG-IDA regimen. After 44 cycles of FLAG-IDA or FLAG regimen, 10/25 (40%) children were nonresponders, 15/25 (60.0%) showed CR. Five (20%) of these patients in CR who underwent allogeneic HSCT are still in remission. The remaining 20 (80.0%) children were lost due to infection or relapse of the primary diseases. The overall survival of patients who are still alive and underwent allogeneic HSCT (mean: 40.6 ± 4.7, median: 40, range: 34-46 months) was longer than that of patients (mean: 5.5 ± 4.3, median: 4, range: 1-15 months) who did not undergo allogeneic HSCT. The CR rate was quite high in the present study using the FLAG-IDA regimen, and the authors believe this regimen is a possible option prior to allogeneic HSCT in children with poor-prognosis acute leukemia.
氟达拉滨、阿糖胞苷、粒细胞集落刺激因子(G-CSF)和伊达比星(FLAG-IDA)方案已被证明是一种对复发或预后不良的儿童白血病可能有效的化疗方案。本研究的目的是评估接受FLAG-IDA方案治疗的预后不良急性白血病患儿的完全缓解(CR)率、毒性和总生存率。此外,作者还调查了接受FLAG-IDA治疗后达到CR的患儿进行异基因造血干细胞移植(HSCT)的适宜性。2002年1月至2007年4月,本中心对25例预后不良的急性白血病患儿采用FLAG-IDA方案进行治疗。在这25例预后不良的急性白血病患儿(16例急性髓系白血病,9例急性淋巴细胞白血病)中,7例(28.0%)接受了1个周期的治疗,17例(68.0%)接受了2个周期的治疗,1例(4%)接受了3个周期的FLAG或FLAG-IDA方案治疗。在进行了44个周期的FLAG-IDA或FLAG方案治疗后,25例患儿中有10例(40%)无反应,15例(60.0%)显示CR。这些CR患者中有5例(20%)接受了异基因HSCT,目前仍处于缓解状态。其余20例(80.0%)患儿因感染或原发性疾病复发而失访。仍存活且接受异基因HSCT的患者的总生存期(平均:40.6±4.7个月,中位数:40个月,范围:34-46个月)长于未接受异基因HSCT的患者(平均:5.5±4.3个月,中位数:4个月,范围:1-15个月)。在本研究中,使用FLAG-IDA方案的CR率相当高,作者认为该方案是预后不良的急性白血病患儿进行异基因HSCT前的一种可能选择。