High-Throughput Screening and Drug Discovery Laboratory, Nemours Center for Childhood Cancer Research, A.I. duPont Hospital for Children , Wilmington, DE , USA.
Front Oncol. 2013 Jul 8;3:170. doi: 10.3389/fonc.2013.00170. eCollection 2013.
Despite dramatic advances in the treatment of pediatric leukemia over the past 50 years, there remain subsets of patients who respond poorly to treatment. Many of the high-risk cases of childhood leukemia with the poorest prognosis have been found to harbor specific genetic signatures, often resulting from chromosomal rearrangements. With increased understanding of the genetic and epigenetic makeup of high-risk pediatric leukemia has come the opportunity to develop targeted therapies that promise to be both more effective and less toxic than current chemotherapy. Of particular importance is an understanding of the interconnections between different targets within the same cancer, and observations of synergy between two different targeted therapies or between a targeted drug and conventional chemotherapy. It has become clear that many cancers are able to circumvent a single specific blockade, and pediatric leukemias are no exception in this regard. This review highlights the most promising approaches to new drugs and drug combinations for high-risk pediatric leukemia. Key biological evidence supporting selection of molecular targets is presented, together with a critical survey of recent progress toward the discovery, pre-clinical development, and clinical study of novel molecular therapeutics.
尽管在过去的 50 年中,儿科白血病的治疗取得了显著进展,但仍有一些患者对治疗反应不佳。许多预后最差的儿童白血病高危病例都存在特定的遗传特征,这些特征通常是由染色体重排引起的。随着对高危儿科白血病的遗传和表观遗传构成的理解不断加深,人们有机会开发出靶向治疗方法,这些方法有望比目前的化疗更有效、毒性更小。特别重要的是要了解同一癌症中不同靶点之间的相互联系,以及两种不同的靶向治疗方法或靶向药物与传统化疗之间的协同作用。事实已经很清楚,许多癌症能够规避单一的特定阻断,儿科白血病在这方面也不例外。这篇综述强调了高危儿科白血病新药和药物组合最有前途的方法。本文提出了支持选择分子靶点的关键生物学证据,并对新型分子治疗药物的发现、临床前开发和临床研究的最新进展进行了批判性调查。