Bassan R, Cortelazzo S, Rambaldi A, Cornelli P, Borleri G, Bellavita P, Biondi A, Barbui T
Divisione di Ematologia, Ospedali Riuniti, Bergamo, Italy.
Bone Marrow Transplant. 1995 May;15(5):791-3.
The prognosis of AML patients who fail autologous BMT and lack a donor for a salvage allogeneic BMT is very poor. We administered an alternative drug treatment including autologous PBSC transplant to a child who relapsed with AML 4 years after a mafosfamide-purged and TBI-containing BMT for second remission AML. Treatment comprised induction-consolidation with 'short' ICE courses (idarubicin-Ara C-etoposide for 2 days), high-dose CY plus G-CSF with collection of CD34+ PBSC and myeloablative treatment with high-dose mitoxantrone/BEAM supported by autologous PBSC reinfusion. The outcome was complete response, lasting 24 months. The patient died in remission of drug-related cardiotoxicity. This report emphasizes the possibility of a secondary AML after mafosfamide-purge autologous BMT, and documents the feasibility of an autologous PBSC transplant in such a high risk setting.
对于自体骨髓移植失败且缺乏供体进行挽救性异基因骨髓移植的急性髓系白血病(AML)患者,预后非常差。我们对一名儿童进行了包括自体外周血干细胞移植在内的替代药物治疗,该儿童在接受马磷酰胺清除和含全身照射(TBI)的骨髓移植以治疗第二次缓解期AML 4年后复发。治疗包括用“短程”ICE方案(伊达比星-阿糖胞苷-依托泊苷,为期2天)进行诱导巩固治疗、高剂量环磷酰胺加粒细胞集落刺激因子(G-CSF)并采集CD34+外周血干细胞,以及在自体外周血干细胞回输支持下用高剂量米托蒽醌/卡莫司汀、依托泊苷、阿糖胞苷、美法仑(BEAM)进行清髓治疗。结果是完全缓解,持续了24个月。患者死于与药物相关的心脏毒性缓解期。本报告强调了马磷酰胺清除自体骨髓移植后发生继发性AML的可能性,并记录了在这种高风险情况下进行自体外周血干细胞移植的可行性。