Loh Mignon L, Rubnitz Jeffrey E
Department of Pediatric Hematology-Oncology, University of California-San Francisco, San Francisco, California 94143-0519, USA.
Curr Opin Hematol. 2002 Jul;9(4):345-52. doi: 10.1097/00062752-200207000-00013.
This article presents the most recent insights into the biology, prognostic significance, and therapeutic approaches to TEL/AML1-positive leukemia. The TEL/AML1 fusion gene, also known as ETV6 /CBFA2, is the most commonly occurring gene rearrangement in pediatric acute lymphoblastic leukemia (ALL). Considerable controversy exists over its prognostic significance with currently available therapies. Differences in outcome may be explained by the differing intensities of various chemotherapy regimens, individual host responses to chemotherapy, or the hypothesis that relapsed TEL/AML1-positive leukemia represents an outgrowth of a secondary leukemia that shares a common initiating event with the first. Incorporating knowledge of this gene rearrangement into treatment decisions serves as a paradigm for translating molecular discoveries into clinically meaningful data to direct patient care and improve outcome.
本文介绍了对TEL/AML1阳性白血病的生物学特性、预后意义及治疗方法的最新见解。TEL/AML1融合基因,也称为ETV6/CBFA2,是小儿急性淋巴细胞白血病(ALL)中最常见的基因重排。关于其在现有治疗中的预后意义存在相当大的争议。结果的差异可能由各种化疗方案的强度不同、个体宿主对化疗的反应不同,或者复发性TEL/AML1阳性白血病代表与首次白血病有共同起始事件的继发性白血病的进展这一假说来解释。将这种基因重排的知识纳入治疗决策,为将分子发现转化为具有临床意义的数据以指导患者护理并改善结果提供了一个范例。