Suppr超能文献

[儿童急性非淋巴细胞白血病的治疗进展(1968 - 1990年)]

[Evolution of the treatment of acute nonlymphoblastic leukemias in children (1968-1990)].

作者信息

Ortega Aramburu J J, Olive Oliveras T, Javier Manchón G, Bastida Vila P

机构信息

Servicio de Hematología, Hospital M-Infantil Vall d'Hebrón, Barcelona.

出版信息

An Esp Pediatr. 1991 Sep;35(3):157-63.

PMID:1741570
Abstract

Changes in treatment of ANLL in children over 23 years (1968-90) and advances made in the last ten years in a pediatric hematological unit are reported herein. Of 124 patients under 15 years of age, 18 of whom were infants, 118 were evaluable. Of these, 58 were treated before 1980 and, although complete remission (CR) was attained in 75%, the median duration was lower than 12 months and no patient survived in CR more than 6 years. From 1981 to 1987, 40 patients received one or two induction treatments followed by three consolidations and then blocks of sequential intensive chemotherapy for 12-15 months. CR was attained in 87.5% and event-free survival (EFS) was 22.5% at 8 years: 14% for those treated from 1981 to 1983 and 33% for those included in the ANLL-84 protocol. In 1988, a post-remission protocol with intensification therapy (two high-dose ARA-C treatments combined with mitoxantrone in the first and amsacrine in the second) followed by allogeneic or autologous bone marrow transplant (BMT) was initiated. Of 20 patients included, 17 reached CR (85%) and 16 underwent BMT. EFS of the 20 patients was 65% at 2 years and post-BMT relapse-free survival was 75%. These results are compared with those obtained separately with present intensive chemotherapy protocols and with BMT and it is concluded that intensification treatment followed by BMT (allogeneic or autologous) might constitute an advance in the treatment of children with ANLL.

摘要

本文报告了23年来(1968 - 1990年)儿童急性非淋巴细胞白血病(ANLL)治疗方法的变化以及过去十年在一家儿科血液科所取得的进展。在124例15岁以下患者中,18例为婴儿,118例可进行评估。其中,58例在1980年前接受治疗,尽管75%达到完全缓解(CR),但中位缓解期低于12个月,且无患者在CR状态下存活超过6年。1981年至1987年,40例患者接受了一或两次诱导治疗,随后进行三次巩固治疗,然后进行12 - 15个月的序贯强化化疗。8年时CR率达到87.5%,无事件生存率(EFS)为22.5%:1981年至1983年治疗的患者为14%,纳入ANLL - 84方案的患者为33%。1988年,启动了缓解后强化治疗方案(第一次为两种高剂量阿糖胞苷联合米托蒽醌治疗,第二次为联合安吖啶治疗),随后进行异基因或自体骨髓移植(BMT)。在纳入的20例患者中,17例达到CR(85%),16例接受了BMT。20例患者的2年EFS为65%,BMT后无复发生存率为75%。将这些结果与目前单独使用强化化疗方案和BMT所获得的结果进行了比较,得出结论:强化治疗后进行BMT(异基因或自体)可能是儿童ANLL治疗的一项进展。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验