von Bueltzingsloewen A, Esperou-Bourdeau H, Souillet G, Demeocq F, Mechinaud-Lacroix F, Michel G, Sadoun A, Bernaudin F, Cornu G, Donadieu J
Hôpital d'Enfants, Nancy, France.
Bone Marrow Transplant. 1995 Oct;16(4):521-7.
A subgroup of children with ALL remains at high risk of relapse despite the administration of intensive chemotherapeutic protocols and may benefit from allogeneic BMT. The cytoreductive regimen used most often combines TBI with cyclophosphamide. Nevertheless, miscellaneous long-term sequelae have been consequent upon radiotherapy, especially in young children. This retrospective multicentric study analyzes the outcome of children with ALL under 4 years of age receiving an HLA-genoidentical BMT following a radiation-free preparative regimen. A busulfan-based regimen with cyclophosphamide or melphalan +/- etoposide +/- cytarabine was given to 21 children (median age: 28 months, range 6-48). Sixteen patients with initial poor prognostic factors were transplanted in first complete response (CR) and five patients in relapse or second CR. With a median follow-up of 47 months, the results show an overall 4-year DFS of 61.1%. Leukemic recurrence was observed in eight patients. The preparative regimen was well-tolerated and there were no transplant-related deaths. A busulfan-based BMT preparative regimen may be a therapeutic alternative to TBI-containing regimens in young children. Efforts are currently aimed at reducing the relapse rate in these children by optimizing the tumoricidal potential of chemotherapy and the graft-versus-leukemia effect of allogeneic BMT.
尽管采用了强化化疗方案,但仍有一部分急性淋巴细胞白血病(ALL)患儿复发风险很高,可能从异基因骨髓移植(BMT)中获益。最常使用的细胞减灭方案是将全身照射(TBI)与环磷酰胺联合使用。然而,放疗会导致各种长期后遗症,尤其是在幼儿中。这项回顾性多中心研究分析了4岁以下接受无辐射预处理方案的HLA基因相同BMT的ALL患儿的预后。21名儿童(中位年龄:28个月,范围6 - 48个月)接受了基于白消安的方案,联合环磷酰胺或美法仑+/-依托泊苷+/-阿糖胞苷。16名初始预后不良因素的患者在首次完全缓解(CR)时接受了移植,5名复发或第二次CR的患者接受了移植。中位随访47个月,结果显示4年总无病生存率(DFS)为61.1%。8名患者出现白血病复发。预处理方案耐受性良好,无移植相关死亡。基于白消安的BMT预处理方案可能是幼儿含TBI方案的一种治疗替代方案。目前的努力旨在通过优化化疗的杀瘤潜力和异基因BMT的移植物抗白血病效应来降低这些儿童的复发率。