Loh Mignon L, Goldwasser Meredith A, Silverman Lewis B, Poon Wing-Man, Vattikuti Shashaank, Cardoso Angelo, Neuberg Donna S, Shannon Kevin M, Sallan Stephen E, Gilliland D Gary
Department of Pediatrics, Comprehensive Cancer Center, University of California, San Francisco, CA 94143, USA.
Blood. 2006 Jun 1;107(11):4508-13. doi: 10.1182/blood-2005-08-3451. Epub 2006 Feb 21.
In a retrospective analysis, we previously reported that children whose leukemia cells harbored the TEL/AML1 gene rearrangement have excellent outcomes. From 1996 to 2000, we conducted a prospective study to determine the incidence and outcomes of children with TEL/AML1-positive acute lymphoblastic leukemia (ALL). Children with newly diagnosed ALL were treated on DFCI ALL Consortium Protocol 95-01. Patients were risk stratified primarily by current National Cancer Institute (NCI)-Rome risk criteria. With a median follow-up of 5.2 years, the 5-year event-free survival for TEL/AML1-positive patients was 89% compared with 80% for TEL/AML1-negative B-precursor patients (P = .05). The 5-year overall survival rate was 97% among TEL/AML-positive patients compared with 89% among TEL/AML1-negative patients (P = .03). However, in a multivariable analysis, risk group (age and leukocyte count at diagnosis) and asparaginase treatment group, but not TEL/AML1 status, were found to be independent predictors of outcome. We conclude that TEL/AML1-positive patients have excellent outcomes, confirming our previous findings. However, factors such as age at diagnosis and presenting leukocyte count should be taken into consideration when treating this group of patients.
在一项回顾性分析中,我们之前报告过白血病细胞携带TEL/AML1基因重排的儿童预后良好。1996年至2000年,我们开展了一项前瞻性研究,以确定TEL/AML1阳性急性淋巴细胞白血病(ALL)患儿的发病率和预后情况。新诊断为ALL的患儿按照DFCI ALL协作组方案95-01进行治疗。患者主要根据当前美国国立癌症研究所(NCI)-罗马风险标准进行风险分层。中位随访5.2年,TEL/AML1阳性患者的5年无事件生存率为89%,而TEL/AML1阴性B前体患者为80%(P = 0.05)。TEL/AML阳性患者的5年总生存率为97%,TEL/AML1阴性患者为89%(P = 0.03)。然而,在多变量分析中,发现风险组(诊断时的年龄和白细胞计数)和天冬酰胺酶治疗组而非TEL/AML1状态是预后的独立预测因素。我们得出结论,TEL/AML1阳性患者预后良好,证实了我们之前的发现。然而,在治疗这组患者时应考虑诊断时的年龄和就诊时的白细胞计数等因素。