Infant leukaemia: clinical, biological and therapeutic advances.

Matteo Luciani, Ippolita Rana, Valecia Pansini, Mauzilio Caniglia, Valentina Coletti, Alice Maraschini, Alessandra Lombardi, Giulio De Rossi
{"title":"Infant leukaemia: clinical, biological and therapeutic advances.","authors":"Matteo Luciani, Ippolita Rana, Valecia Pansini, Mauzilio Caniglia, Valentina Coletti, Alice Maraschini, Alessandra Lombardi, Giulio De Rossi","doi":"10.1111/j.1651-2227.2006.tb02416.x","DOIUrl":null,"url":null,"abstract":"<p><strong>Unlabelled: </strong>Infant acute lymphoid leukaemia (IALL) represents a distinct subset with an extremely poor response to therapy, despite major progress in the treatment of childhood leukaemia. However, several studies have shown that, even in this generally considered homogeneous group, a distinction could be made with regard to prognosis. The outcome of IALL patients with ALL-1/MLL rearrangements at the 11q23 cytogenetic band, early pre-B immunophenotype, high WBC count and age below 6 mo is significantly worse than in patients without these characteristics, and current therapies appear inadequate in a significant number of cases. Therefore, an international protocol (Interfant 99) was recently started, using a more aggressive approach, which included lymphoid- and myeloid-specific drugs, and indications for stem-cell transplantation. We reviewed the clinical characteristics of the disease, the results of several recent international clinical trials, and our experience with 16 infants with acute lymphoid leukaemia diagnosed and treated at our institution.</p><p><strong>Conclusion: </strong>It is extremely important to stratify patients for prognosis, taking into account clinical and biological variables with independent prognostic value. The aim is to select more adequate, risk-adapted, therapeutic strategies which also consider related or unrelated bone marrow transplant consolidation for patients with very poor prognosis.</p>","PeriodicalId":76973,"journal":{"name":"Acta paediatrica (Oslo, Norway : 1992). Supplement","volume":"95 452","pages":"47-51"},"PeriodicalIF":0.0000,"publicationDate":"2006-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta paediatrica (Oslo, Norway : 1992). Supplement","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/j.1651-2227.2006.tb02416.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Unlabelled: Infant acute lymphoid leukaemia (IALL) represents a distinct subset with an extremely poor response to therapy, despite major progress in the treatment of childhood leukaemia. However, several studies have shown that, even in this generally considered homogeneous group, a distinction could be made with regard to prognosis. The outcome of IALL patients with ALL-1/MLL rearrangements at the 11q23 cytogenetic band, early pre-B immunophenotype, high WBC count and age below 6 mo is significantly worse than in patients without these characteristics, and current therapies appear inadequate in a significant number of cases. Therefore, an international protocol (Interfant 99) was recently started, using a more aggressive approach, which included lymphoid- and myeloid-specific drugs, and indications for stem-cell transplantation. We reviewed the clinical characteristics of the disease, the results of several recent international clinical trials, and our experience with 16 infants with acute lymphoid leukaemia diagnosed and treated at our institution.

Conclusion: It is extremely important to stratify patients for prognosis, taking into account clinical and biological variables with independent prognostic value. The aim is to select more adequate, risk-adapted, therapeutic strategies which also consider related or unrelated bone marrow transplant consolidation for patients with very poor prognosis.

婴儿白血病:临床、生物学和治疗进展。
未标记:尽管儿童白血病的治疗取得了重大进展,但婴儿急性淋巴细胞白血病(IALL)是一个对治疗反应极差的独特亚群。然而,一些研究表明,即使在这个通常被认为是同质的群体中,也可以在预后方面做出区分。11q23细胞遗传带ALL-1/MLL重排、早期b前免疫表型、高WBC计数和年龄小于6个月的IALL患者的预后明显差于没有这些特征的患者,并且目前的治疗方法在相当数量的病例中显得不足。因此,最近开始了一项国际协议(interant 99),采用了一种更积极的方法,包括淋巴细胞和骨髓特异性药物,以及干细胞移植的适应症。我们回顾了该疾病的临床特征,最近几项国际临床试验的结果,以及我们在我院诊断和治疗的16例急性淋巴性白血病婴儿的经验。结论:考虑具有独立预后价值的临床和生物学变量,对患者进行预后分层极为重要。目的是为预后非常差的患者选择更充分、更适合风险的治疗策略,同时考虑相关或不相关的骨髓移植巩固。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信