Suppr超能文献

成人急性淋巴细胞白血病

Adult acute lymphoblastic leukemia.

作者信息

Jabbour Elias J, Faderl Stefan, Kantarjian Hagop M

机构信息

Department of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Mayo Clin Proc. 2005 Nov;80(11):1517-27. doi: 10.4065/80.11.1517.

Abstract

Much progress has been made in understanding the biology of and therapy for acute lymphoblastic leukemia (ALL). This progress has translated into the recognition of several subgroups of ALL and the institution of risk-adapted therapies. New therapies are emerging based on the definition of specific cytogenetic-molecular abnormalities. Changes in the pathologic classification of ALL have led to therapeutic consequences. Adaptation of successful treatment strategies in children with ALL has resulted in similar complete remission rates in adults. Prognosis has Improved especially in mature B-cell ALL and T-cell lineage ALL. However, regardless of ALL subgroup, long-term survival in adults is still inferior to that in children. Development of new drugs and agents tailored to subset-specific cytogenetic-molecular characteristics is vital to the therapeutic success in adult ALL.

摘要

在理解急性淋巴细胞白血病(ALL)的生物学特性及治疗方面已取得了很大进展。这一进展已转化为对ALL几个亚组的认识以及风险适应性治疗的实施。基于特定细胞遗传学-分子异常的定义,新的治疗方法正在涌现。ALL病理分类的变化已产生了治疗上的影响。将儿童ALL成功的治疗策略应用于成人,已使成人的完全缓解率相近。预后尤其在成熟B细胞ALL和T细胞系ALL中有所改善。然而,无论ALL亚组如何,成人的长期生存率仍低于儿童。开发针对亚组特异性细胞遗传学-分子特征的新药和药物对于成人ALL的治疗成功至关重要。

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