Suppr超能文献

采用综合方法治疗儿童复发性急性淋巴细胞白血病的六年经验(ALL-REZ BFM 85)。BFM组的一项复发研究。

Six-year experience with a comprehensive approach to the treatment of recurrent childhood acute lymphoblastic leukemia (ALL-REZ BFM 85). A relapse study of the BFM group.

作者信息

Henze G, Fengler R, Hartmann R, Kornhuber B, Janka-Schaub G, Niethammer D, Riehm H

机构信息

Department of Hematology and Oncology, University Children's Hospital, Berlin, Germany.

出版信息

Blood. 1991 Sep 1;78(5):1166-72.

PMID:1878583
Abstract

Between April 1985 and March 1987 130 children and adolescents up to 18 years of age with first relapse of acute lymphoblastic leukemia (ALL) were registered on the stratified and randomized multicentric trial ALL-REZ BFM 85 designed for patients pretreated with intensive front-line therapies. Stratification criteria were time and site of relapse: bone marrow (BM) relapse on or up to 6 months after stopping front-line therapy (group A), BM relapse beyond 6 months after therapy (group B), and isolated extramedullary relapse at any time (group C). Treatment consisted of alternating courses of polychemotherapy including randomly administered high- or intermediate-dose methotrexate (HDMTX:12 g/m2 as 4-hour infusion; IDMTX: 1 g/m2 as 36-hour infusion). During maintenance therapy the patients received daily oral thioguanine and biweekly intravenous (IV) MTX. The overall second complete remission (CR) rate was 92% (groups A, B, and C: 88%, 92%, and 100%), and the probability of event-free survival (EFS) at 6 years is 0.31 +/- 0.04 (groups A, B, and C: 0.18 +/- 0.05, 0.30 +/- 0.07, and 0.72 +/- 0.11). HDMTX did not prove to be superior to IDMTX, which led to premature stopping of randomization. Risk factor analyses showed early relapse, particularly BM relapse within 18 months, and T-cell phenotype to be independent predictors of poor outcome. The incidence of central nervous system (CNS) relapses following BM relapse was 19%, indicating that reprophylaxis to the CNS with IV/intrathecal (IT) MTX was insufficient. For 17 children who received bone marrow transplantation in second CR from HLA-compatible siblings the EFS was 0.53 +/- 0.12 at 5 years. Their outcome was not influenced by the above-mentioned risk factors. With the proposed treatment regimen long-lasting second remissions can be achieved in about one third of patients even after intensive front-line treatment.

摘要

1985年4月至1987年3月期间,130名18岁及以下急性淋巴细胞白血病(ALL)首次复发的儿童和青少年被纳入了针对接受过强化一线治疗的患者设计的分层随机多中心试验ALL-REZ BFM 85。分层标准为复发时间和部位:在停止一线治疗后6个月内或6个月时发生骨髓(BM)复发(A组),治疗后6个月后发生BM复发(B组),以及在任何时间发生孤立的髓外复发(C组)。治疗包括交替进行的多药化疗疗程,其中随机给予高剂量或中剂量甲氨蝶呤(HDMTX:12 g/m²,4小时输注;IDMTX:1 g/m²,36小时输注)。在维持治疗期间,患者每日口服硫鸟嘌呤,并每两周静脉注射(IV)甲氨蝶呤。总体第二次完全缓解(CR)率为92%(A、B和C组分别为88%、92%和100%),6年无事件生存(EFS)概率为0.31±0.04(A、B和C组分别为0.18±0.05、0.30±0.07和0.72±0.11)。HDMTX并未被证明优于IDMTX,这导致随机分组提前终止。危险因素分析显示,早期复发,尤其是18个月内的BM复发,以及T细胞表型是预后不良的独立预测因素。BM复发后中枢神经系统(CNS)复发的发生率为19%,表明采用IV/鞘内(IT)甲氨蝶呤对CNS进行再预防是不足的。对于17名在第二次CR时接受来自HLA相合同胞的骨髓移植的儿童,5年EFS为0.53±0.12。他们的预后不受上述危险因素的影响。采用所建议的治疗方案,即使在强化一线治疗后,约三分之一的患者也能实现持久的第二次缓解。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验