异基因骨髓移植在首次缓解中拯救费城染色体阳性急性淋巴细胞白血病儿童:东京儿童癌症研究小组(TCCSG)研究L89-12和L92-13。

T. Mori, A. Manabe, M. Tsuchida, R. Hanada, H. Yabe, A. Ohara, T. Saito, S. Nakazawa
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引用次数: 24

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,来自大型研究的报道很少。我们评估了同种异体骨髓移植(alloo - bmt)治疗儿童这种类型白血病的疗效。化疗方案包括诱导期和非常强化的巩固,然后是再诱导期和晚期强化治疗。治疗方式的选择,如化疗、同种异体骨髓移植或自体移植由各研究所决定。根据治疗方案,主要终点是Ph(+) ALL患儿的结局。结果1989 - 1994年,在东京儿童癌症研究组(TCCSG)连续入选的741例ALL患者中,32例(4.3%)被诊断为Ph(+) ALL。30例(93.8%)患者完全缓解(CR)。在这30名患者中,有8名儿童在第一次CR中选择性地接受了alloo - bmt治疗。其中6名患者在诊断后的中位随访时间为58个月(范围48-105个月),持续缓解。1例患者死于复发,另1例患者死于移植物抗宿主病。在第一次CR中,3例接受自体骨髓移植或外周血干细胞移植治疗的患者随后复发。其余19例患者中,13例患者单独接受高危化疗,均在28个月内复发。一名患者被排除在分析之外,因为他接受了标准风险化疗直到复发。其他5名患者也被排除在分析之外,因为直到他们复发才检测到费城染色体。尽管接受了包括allo-BMT在内的治疗,但没有复发患者存活。在多变量分析中,只有allo-BMT仍然是预后良好的独立因素。结论在本研究中,治疗儿童Ph(+) ALL的唯一方法是allo-BMT,其结果似乎很有希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.
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.
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