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Hematopoietic stem cell transplantation with conditioning regimens containing melphalan in pediatric patients with acute lymphoblastic leukemia

机译:含美法仑的调理方案造血干细胞移植在小儿急性淋巴细胞白血病患者中的应用

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A multicenter comparative study was carried out to investigate the efficacy and safety of hematopoietic stem cell transplantation with conditioning regimens containing melphalan in pediatric patients with acute lymphoblastic leukemia. One hundred twenty three patients at a variety of remission stages were eligible for study participation. Eighty-nine were transplanted with allogeneic grafts and 34 patients with autologous grafts (23 cases with bone marrow and 11 cases with peripheral blood stem cells). Conditioning regimens used were as follows: (A) melphalan and busulfan for 40 patients, (B) melphalan, busulfan and TBI for 44 patients, (C) other regimens for 39 patients. To accelerate engraftment G-CSF (lenograstim) was administered as a 1-hour or 24-hour drip infusion daily at 5 micrograms/kg from day 5 until hematological recovery. The five year disease free survival (DFS) was 63% for 42 patients at CR 1, 41% for 41 patients at CR 2 and 33% for 40 patients at other stages. There was no significant difference in the DFS between allogeneic-transplantation and autologous-transplantation in all disease stages. In patients at remission stage for CR 1 and CR 2, the 5-year DFS by conditioning regimen was 63% for regimen (A), 54% for regimen (B) and 54% for regimens with melphalan and TBI. There was no significant difference in the DFS between the groups. Serious complications such as renal failure were observed in 11%, veno-occlusive disease in 9%, and interstitial pneumonia in 9%. The most dominating cause of death was relapse in the disease (48% of deaths) which was most commonly observed in autologous transplantation. Contrary to that, treatment related toxic death was the most frequent cause of deaths in allogeneic-transplantation.
机译:进行了一项多中心比较研究,以研究含美法仑的调理方案对小儿急性淋巴细胞白血病患者造血干细胞移植的疗效和安全性。 123个处于不同缓解阶段的患者有资格参加研究。异体移植89例,自体移植34例(骨髓23例,外周血干细胞11例)。使用的条件疗法如下:(A)美法仑和白消安40例,(B)美法仑,白消安和TBI 44例,(C)其他方案39例。为了加速植入,从第5天开始,以5微克/千克的剂量每天1小时或24小时滴注G-CSF(来诺格司亭)直至血液学恢复。在CR 1时有42例患者的5年无病生存率(DFS)为63%,在CR 2时为41%的患者为41%,其他阶段的40例为33%。在所有疾病阶段,同种异体移植和自体移植之间的DFS没有显着差异。在CR 1和CR 2缓解期的患者中,通过条件疗法的5年DFS方案(A)为63%,方案(B)为54%,美法仑和TBI方案为54%。两组之间的DFS没有显着差异。观察到严重的并发症,如肾功能衰竭(11%),静脉阻塞性疾病(9%)和间质性肺炎(9%)。死亡的最主要原因是疾病的复发(占死亡的48%),这是在自体移植中最常见的情况。与此相反,在异基因移植中,与治疗有关的毒性死亡是最常见的死亡原因。

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