Ghazavi Farzaneh, Clappier Emmanuelle, Lammens Tim, Suciu Stefan, Caye Aurélie, Zegrari Samira, Bakkus Marleen, Grardel Nathalie, Benoit Yves, Bertrand Yves, Minckes Odile, Costa Vitor, Ferster Alina, Mazingue Françoise, Plat Geneviève, Plouvier Emmanuel, Poirée Marilyne, Uyttebroeck Anne, van der Werff-Ten Bosch Jutte, Yakouben Karima, Helsmoortel Hetty, Meul Magali, Van Roy Nadine, Philippé Jan, Speleman Frank, Cavé Hélène, Van Vlierberghe Pieter, De Moerloose Barbara
Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Belgium Center for Medical Genetics, Ghent University Hospital, Belgium.
Department of Genetics, Robert Debré Hospital, APHP, Paris, France Hematology University Institute, University Paris-Diderot, Paris, France.
Haematologica. 2015 Oct;100(10):1311-9. doi: 10.3324/haematol.2015.126953. Epub 2015 Jul 2.
DNA copy number analysis has been instrumental for the identification of genetic alterations in B-cell precursor acute lymphoblastic leukemia. Notably, some of these genetic defects have been associated with poor treatment outcome and might be relevant for future risk stratification. In this study, we characterized recurrent deletions of CD200 and BTLA genes, mediated by recombination-activating genes, and used breakpoint-specific polymerase chain reaction assay to screen a cohort of 1154 cases of B-cell precursor acute lymphoblastic leukemia uniformly treated according to the EORTC-CLG 58951 protocol. CD200/BTLA deletions were identified in 56 of the patients (4.8%) and were associated with an inferior 8-year event free survival in this treatment protocol [70.2% ± 1.2% for patients with deletions versus 83.5% ± 6.4% for non-deleted cases (hazard ratio 2.02; 95% confidence interval 1.23-3.32; P=0.005)]. Genetically, CD200/BTLA deletions were strongly associated with ETV6-RUNX1-positive leukemias (P<0.0001), but were also identified in patients who did not have any genetic abnormality that is currently used for risk stratification. Within the latter population of patients, the presence of CD200/BTLA deletions was associated with inferior event-free survival and overall survival. Moreover, the multivariate Cox model indicated that these deletions had independent prognostic impact on event-free survival when adjusting for conventional risk criteria. All together, these findings further underscore the rationale for copy number profiling as an important tool for risk stratification in human B-cell precursor acute lymphoblastic leukemia. This trial was registered at www.ClinicalTrials.gov as #NCT00003728.
DNA拷贝数分析对于识别B细胞前体急性淋巴细胞白血病中的基因改变具有重要作用。值得注意的是,其中一些基因缺陷与治疗效果不佳相关,可能与未来的风险分层有关。在本研究中,我们对由重组激活基因介导的CD200和BTLA基因的复发性缺失进行了特征分析,并使用断点特异性聚合酶链反应检测法对按照欧洲癌症研究与治疗组织儿童白血病协作组(EORTC-CLG)58951方案统一治疗的1154例B细胞前体急性淋巴细胞白血病病例进行了筛查。在56例患者(4.8%)中发现了CD200/BTLA缺失,在该治疗方案中,这与较差的8年无事件生存率相关[缺失患者为70.2%±1.2%,未缺失病例为83.5%±6.4%(风险比2.02;95%置信区间1.23 - 3.32;P = 0.005)]。从遗传学角度来看,CD200/BTLA缺失与ETV6-RUNX1阳性白血病密切相关(P<0.0001),但在没有任何当前用于风险分层的基因异常的患者中也被发现。在后者这群患者中,CD200/BTLA缺失的存在与较差的无事件生存率和总生存率相关。此外,多变量Cox模型表明,在调整传统风险标准后,这些缺失对无事件生存率具有独立的预后影响。总之,这些发现进一步强调了拷贝数分析作为人类B细胞前体急性淋巴细胞白血病风险分层重要工具的基本原理。该试验已在www.ClinicalTrials.gov上注册,编号为#NCT000037