Hashmi Khalil Ullah, Khan Badshah, Ahmed Parvez, Raza Shahid, Hussain Iftikhar, Mahmood Ahsan, Iqbal Hamid, Malik Hamid Saeed, Anwar Masood
Armed Forces Bone Marrow Transplant Centre, Rawalpindi.
J Pak Med Assoc. 2005 Jun;55(6):234-8.
To evaluate the efficacy and toxicity profile of the combination of fludarabine, high dose cytarabine, idarubicin, and granulocyte colony stimulating factor in refractory relapsed cases of acute leukaemia, a study is being conducted at Armed Forces Bone Marrow Transplant Centre (AFBMTC) Rawalpindi since January 2003. Data up to June 2004 (early report) is being presented.
Twelve Patients with refractory/relapsed (Ref/Rel) acute leukaemia (AL) were treated with fludarabine 30 mg/m2 and cytosine arabinoside (AraC) Arac 2 g/m2 for 5 days, idarubicin 10 mg/m2 for 3 days, and granulocyte colony stimulating factor G-CSF 5 micro g/kg from day 0 till neutrophil recovery (ANC > 1.0 x 10(9)/1). Response was evaluated by bone marrow examination on day 20-post chemotherapy.
Patients included were refractory acute lymphoblastic leukaemia (ALL) (n=2), relapsed ALL (n = 3), refractory acute myeloid leukaemia (AML) (n = 3), secondary AML (n=2) relapsed AML (n = 1) and acute undifferentiated leukaemia (AUL) (n = 1). Complete remission (CR) was achieved in 8 (66.6%) patients. Three (25%) patients died of post chemotherapy complications and one patient failed to achieve remission. Out of 8 patients who achieved CR, 4 underwent allogeneic bone marrow transfusion (BMT), 1 is being evaluated for the same, 1 received idorubicin, AraC and etopuside (ICE) and high dose AraC, 1 did not receive further chemotherapy and 1 relapsed two months after remission. Seven patients are still in CR after a median follow up of 8 months (range 3-18). Major complications encountered were diarrhoea, mucositis, toxic ileus, transient hepatic toxicity, fungal and bacterial infections.
In our experience, FLAG-IDA is well tolerated and effective regimen in relapsed/refractory acute leukaemias. The toxicity is acceptable, enabling most patients to receive further treatment, including transplantation procedures.
为评估氟达拉滨、大剂量阿糖胞苷、伊达比星和粒细胞集落刺激因子联合应用于急性白血病难治性复发病例的疗效和毒性特征,自2003年1月起在拉瓦尔品第武装部队骨髓移植中心(AFBMTC)开展了一项研究。本文呈现了截至2004年6月的数据(早期报告)。
12例难治性/复发性(Ref/Rel)急性白血病(AL)患者接受治疗,氟达拉滨30mg/m²、阿糖胞苷(AraC)2g/m²,持续5天,伊达比星10mg/m²,持续3天,从第0天开始至中性粒细胞恢复(中性粒细胞绝对值>1.0×10⁹/L)给予粒细胞集落刺激因子G-CSF 5μg/kg。化疗后第20天通过骨髓检查评估疗效。
纳入患者包括难治性急性淋巴细胞白血病(ALL)(n = 2)、复发性ALL(n = 3)、难治性急性髓系白血病(AML)(n = 3)、继发性AML(n = 2)、复发性AML(n = 1)和急性未分化白血病(AUL)(n = 1)。8例(66.6%)患者达到完全缓解(CR)。3例(25%)患者死于化疗后并发症,1例患者未达到缓解。在达到CR的8例患者中,4例接受了异基因骨髓移植(BMT),1例正在评估,1例接受了伊达比星、阿糖胞苷和依托泊苷(ICE)以及大剂量阿糖胞苷治疗,1例未接受进一步化疗,1例缓解后2个月复发。中位随访8个月(范围3 - 18个月)后,7例患者仍处于CR状态。主要并发症包括腹泻、黏膜炎、中毒性肠麻痹、短暂性肝毒性、真菌和细菌感染。
根据我们的经验,FLAG-IDA方案在复发性/难治性急性白血病中耐受性良好且有效。毒性是可接受的,使大多数患者能够接受进一步治疗,包括移植手术。