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Results of 58872 and 58921 trials in acute myeloblastic leukemia and relative value of chemotherapy vs allogeneic bone marrow transplantation in first complete remission: the EORTC Children Leukemia Group report

机译:EORTC儿童白血病小组报告:急性完全粒细胞白血病的58872和58921试验结果以及化学疗法与同种异体骨髓移植相对于首次完全缓解的相对价值

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摘要

The first EORTC (European Organization of Research and Treatment of Cancer) acute myeloblastic leukemia (AML) pilot study (58872) was conducted between January 1988 and December 1991. Out of 108 patients, 78% achieved complete remission (CR), and event-free survival (EFS) and survival rates (s.e., %) at 7 years were 40 (5) and 51% (6%), respectively. It indicated that mitoxantrone could be substituted for conventional anthracyclines in the treatment of childhood AML without inducing cardiotoxicity. The aim of the next EORTC 58921 trial was to compare the efficacy and toxicity of idarubicin vs mitoxantrone in initial chemotherapy courses, further therapy consisting of allogeneic bone marrow transplantation (alloBMT) in patients with an HLA-compatible sibling donor or chemotherapy in patients without a donor. Out of 177 patients, recruited between October 1992 and December 2002, 81% reached CR. Overall 7-year EFS and survival rates were 49 (4) and 62% (4%), respectively. Out of 145 patients who received the first intensification, 39 had a sibling donor. In patients with or without a donor, the 7-year disease-free survival (DFS) rate was 63 (8) and 57% (5%) and the 7-year survival rate was 78 (7) and 65% (5%), respectively. Patients with favorable, intermediate and unfavorable cytogenetic features had a 5-year EFS rate of 57, 45 and 45% and a 5-year survival rate of 89, 67 and 53%, respectively.
机译:1988年1月至1991年12月进行了第一项EORTC(欧洲癌症研究和治疗组织)急性粒细胞性白血病(AML)初步研究(58872)。在108例患者中,有78%达到了完全缓解(CR),并且7年的免费生存(EFS)和生存率(se,%)分别为40(5)和51%(6%)。这表明米托蒽醌可以替代常规蒽环类药物治疗儿童AML,而不会引起心脏毒性。下一次EORTC 58921试验的目的是比较伊达比星与米托蒽醌在初始化疗过程中的疗效和毒性,对具有HLA相容性同胞供体的患者进行同种异体骨髓移植(alloBMT)的进一步治疗,或对未接受过HLA治疗的患者进行化学治疗捐赠者。在1992年10月至2002年12月期间招募的177例患者中,有81%达到了CR。总体7年EFS和生存率分别为49(4)和62%(4%)。在接受第一次强化治疗的145位患者中,有39位有同胞供体。在有或没有供体的患者中,7年无病生存率(DFS)分别为63(8)和57%(5%),7年生存率分别为78(7)和65%(5%) ), 分别。具有良好,中度和不利细胞遗传学特征的患者的5年EFS率分别为57%,45%和45%,5年生存率分别为89%,67%和53%。

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