Ortega Juan J, Díaz de Heredia Cristina, Olivé Teresa, Bastida Pilar, Llort Anna, Armadans Lluís, Torrabadella Marta, Massuet Lluís
Servicio de Hematologia y Oncologia, Area Infantil, Hospital Universitari Vall d'Hebron, Passeig Vall d'Hebron 119, 08035 Barcelona, Spain.
Haematologica. 2003 Mar;88(3):290-9.
Although chemotherapy in childhood acute myeloid leukemia (AML) has improved in the last decade, except for a group of better-risk patients (approximately one third), more than half the other patients relapse. The main objective of this study was to evaluate the results obtained with bone marrow transplants, either allogeneic (allo-BMT) or autologous (auto-BMT), following two intensive consolidation courses in a series of children with high-risk (HR) AML according to morphologic and early-response BFM criteria. A second objective was to compare the results of auto-BMT with those of allo-BMT.
From April 1988 to May 2001, 79 children (< 15 years old) with de novo AML entered the prospective AML-88 trial in a single institution: 50 (63%) were qualified as having high-risk disease and are the subject of this study. After 1 or 2 induction courses, depending on early response, and two consolidations, patients with an HLA-identical sibling received an allo-BMT and all the others an auto-BMT. The conditioning regimen was cyclophosphamide and total body irradiation (TBI) in children over 3 years old and busulfan and etoposide in younger children. Bone marrow was purged with mafosfamide in auto-BMT and cyclosporine alone was given as graft-versus-host disease (GVHD) prophylaxis in allo-BMT.
At the end of the chemotherapy phase (induction and consolidation ), 46 of the 50 HR patients (92%) had attained complete remission (CR) after one (n=29), two (n=11) or three (n=6) courses; 2 more were in partial remission (PR) and 2 had died. The 48 patients in CR or PR received either an allo-BMT (17) or an auto-BMT (31). Hematologic reconstitution was significantly slower in auto-BMT recipients. Forty-one percent of patients who received allo-BMT suffered acute GVHD grades II-IV. Toxic deaths and relapse rates were 5.9% and 17.6%, respectively, in allo-BMT and 3.2% and 25.8%, respectively, in auto-BMT. Post-transplant 8-year event-free survival (EFS) was 74.5% (54-96) in allo-BMT and 74.2% (59-89) in auto-BMT. EFS and OS in all the series (50 patients) were 71% (59-83) and 73% (61-85), respectively, with a median follow-up of 7.2 years.
This study indicates that improved results in children with HR-AML can be obtained by either allo- or auto-BMT performed after two courses of intensive consolidation therapy provided good supportive therapy is given and reduced transplant -related mortality (TRM) is minimized.
尽管在过去十年中儿童急性髓系白血病(AML)的化疗有所改善,但除了一组风险较低的患者(约三分之一)外,超过半数的其他患者会复发。本研究的主要目的是评估在一系列根据形态学和早期反应BFM标准判定为高危(HR)AML的儿童中,接受两个强化巩固疗程后进行异基因(allo - BMT)或自体(auto - BMT)骨髓移植的结果。第二个目的是比较auto - BMT和allo - BMT的结果。
从1988年4月至2001年5月,79例(<15岁)新发AML儿童进入一家机构的前瞻性AML - 88试验:50例(63%)被判定为患有高危疾病,是本研究的对象。根据早期反应进行1或2个诱导疗程以及两个巩固疗程后,有 HLA 相同同胞的患者接受allo - BMT,其他所有患者接受auto - BMT。3岁以上儿童的预处理方案为环磷酰胺和全身照射(TBI),年幼儿童为白消安和依托泊苷。自体骨髓移植中用马磷酰胺清除骨髓,异基因骨髓移植中仅给予环孢素预防移植物抗宿主病(GVHD)。
在化疗阶段(诱导和巩固)结束时,50例HR患者中有46例(92%)在1个(n = 29)、2个(n = 11)或3个(n = 6)疗程后达到完全缓解(CR);另外2例为部分缓解(PR),2例死亡。48例CR或PR患者接受了allo - BMT(17例)或auto - BMT(31例)。自体骨髓移植受者的血液学重建明显较慢。接受allo - BMT的患者中有41%发生II - IV级急性GVHD。异基因骨髓移植的毒性死亡和复发率分别为5.9%和17.6%,自体骨髓移植分别为3.2%和25.8%。移植后8年无事件生存率(EFS)在allo - BMT中为74.5%(54 - 96),在auto - BMT中为74.2%(59 - 89)。所有系列(50例患者)的EFS和总生存率(OS)分别为71%(59 - 83)和73%(61 - 85),中位随访时间为7.2年。
本研究表明,对于HR - AML儿童,在两个强化巩固疗程后进行allo - BMT或auto - BMT,并给予良好的支持治疗且将与移植相关的死亡率(TRM)降至最低,可取得更好的结果。