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首次缓解期进行异基因骨髓移植可挽救费城染色体阳性急性淋巴细胞白血病患儿:东京儿童癌症研究组(TCCSG)的L89 - 12和L92 - 13研究

Allogeneic bone marrow transplantation in first remission rescues children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Tokyo Children's Cancer Study Group (TCCSG) studies L89-12 and L92-13.

作者信息

Mori T, Manabe A, Tsuchida M, Hanada R, Yabe H, Ohara A, Saito T, Nakazawa S

机构信息

Department of Pediatrics, Social Insurance Saitama Chuo Hospital, Tokyo, Japan.

出版信息

Med Pediatr Oncol. 2001 Nov;37(5):426-31. doi: 10.1002/mpo.1225.

Abstract

BACKGROUND

The prognosis of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph(+) ALL) is generally poor and reports from large studies are scarce. We evaluated the efficacy of allogeneic bone marrow transplantation (allo-BMT) for children with this type of leukemia.

PROCEDURE

The chemotherapy regimens consisted of an induction phase and very intensive consolidation followed by a reinduction phase and late intensification treatment. The selection of treatment modalities such as chemotherapy, allo-BMT, or autologous transplantation was made by each institute. The principal endpoint was the outcome of children with Ph(+) ALL according to the treatment options.

RESULTS

Thirty-two patients (4.3%) were diagnosed as Ph(+) ALL out of the 741 cases of ALL consecutively enrolled in two protocols of the Tokyo Children's Cancer Study Group (TCCSG) from 1989 to 1994. Thirty patients (93.8%) were induced into complete remission (CR). Of these 30 patients, eight children electively received allo-BMT in the first CR. Six of these patients are in continuous remission at a median follow-up of 58 (range 48-105) months after the diagnosis. One patient died following recurrence and another patient died of graft vs. host disease. Three patients treated with autologous BMT or peripheral blood stem cell transplantation in the first CR experienced a subsequent relapse. In the remaining 19 patients, 13 patients were treated with very high-risk chemotherapy alone and all relapsed within 28 months. One patient was excluded from the analysis because he was treated with standard-risk chemotherapy until relapse. The other five patients were also excluded from the analysis because Philadelphia chromosome was not detected until they relapsed. None of the relapsed patients survived in spite of treatment including allo-BMT. In multivariate analysis, only allo-BMT remained as an independent factor for good prognosis.

CONCLUSIONS

The only way to cure children with Ph(+) ALL was allo-BMT in this study and its outcome seemed promising.

摘要

背景

费城染色体阳性急性淋巴细胞白血病(Ph(+) ALL)的预后通常较差,且大型研究报告较少。我们评估了异基因骨髓移植(allo-BMT)对这类白血病患儿的疗效。

程序

化疗方案包括诱导期和强化巩固期,随后是再诱导期和晚期强化治疗。化疗、allo-BMT或自体移植等治疗方式的选择由各机构自行决定。主要终点是根据治疗方案确定的Ph(+) ALL患儿的治疗结果。

结果

在1989年至1994年连续纳入东京儿童癌症研究组(TCCSG)两项方案的741例ALL病例中,32例(4.3%)被诊断为Ph(+) ALL。30例(93.8%)诱导进入完全缓解(CR)。在这30例患者中,8名儿童在首次CR时选择性接受了allo-BMT。其中6例患者在诊断后的中位随访58个月(范围48 - 105个月)时持续缓解。1例患者复发后死亡,另1例患者死于移植物抗宿主病。3例在首次CR时接受自体BMT或外周血干细胞移植治疗的患者随后复发。在其余19例患者中,13例仅接受了高危化疗,均在28个月内复发。1例患者因在复发前接受标准风险化疗而被排除在分析之外。另外5例患者也被排除在分析之外,因为直到复发才检测到费城染色体。尽管包括allo-BMT在内进行了治疗,但复发患者无一存活。多因素分析中,只有allo-BMT是预后良好的独立因素。

结论

本研究中,治愈Ph(+) ALL患儿的唯一方法是allo-BMT且其结果似乎很有前景。

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