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Allogeneic and autologous bone marrow transplantation after consolidation therapy in high-risk acute myeloid leukemia in children. Towards a risk-oriented therapy | Haematologica

机译:儿童高危急性髓细胞白血病巩固治疗后的同种异体和自体骨髓移植。迈向风险导向疗法|血液学

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BACKGROUND AND OBJECTIVES: 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. DESIGN AND METHODS: 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. RESULTS: 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. INTERPRETATION AND CONCLUSIONS: 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.
机译:背景与目的:尽管在过去的十年中,儿童急性髓细胞性白血病(AML)的化疗有所改善,除了一组高风险患者(约三分之一)外,其他患者中有一半以上复发。这项研究的主要目的是在一系列高危(HR)AML儿童中进行两次强化巩固课程后,评估同种异体(allo-BMT)或自体(auto-BMT)骨髓移植获得的结果根据形态学和早期反应BFM标准。第二个目标是比较auto-BMT和allo-BMT的结果。设计与方法:从1988年4月到2001年5月,有79名(<15岁)新生AML儿童在单一机构中参加了前瞻性AML-88试验:50名(63%)被定为高危疾病,本研究的主题。经过1或2次诱导过程后,取决于早期反应和两次合并,具有HLA相同兄弟姐妹的患者接受同种BMT,所有其他患者接受自动BMT。适应方案为3岁以上儿童使用环磷酰胺和全身照射(TBI),年龄较小的儿童使用白消安和依托泊苷。在自体BMT中用mafosfamide清除骨髓,单独给予环孢素作为异体BMT中的移植物抗宿主病(GVHD)预防措施。结果:在化疗阶段结束时(诱导和巩固),在50例HR患者中,有46例(92%)在1例(n = 29),2例(n = 11)或3例(n = 6)课程;另外2人处于部分缓解(PR)状态,另有2人死亡。 CR或PR的48例患者接受了同种BMT(17)或自动BMT(31)。自动BMT接受者的血液学重建明显较慢。接受同种BMT的患者中有41%患有急性GVHD II-IV级。同种BMT的毒性死亡和复发率分别为5.9%和17.6%,而自体BMT的毒性死亡和复发率分别为3.2%和25.8%。同种BMT的移植后8年无事件生存率(EFS)为74.5%(54-96),而自体BMT则为74.2%(59-89)。所有系列(50例患者)的EFS和OS分别为71%(59-83)和73%(61-85),中位随访时间为7.2年。解释和结论:这项研究表明,只要给予了良好的支持治疗并降低了与移植相关的死亡率(TRM),在进行了两个疗程的强化巩固治疗后,通过同种或自动BMT可以对HR-AML患儿取得更好的结果。被最小化。

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