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慢性粒细胞白血病中衍生9号染色体缺失的异质性预后影响

Heterogeneous prognostic impact of derivative chromosome 9 deletions in chronic myelogenous leukemia.

作者信息

Kreil Sebastian, Pfirrmann Markus, Haferlach Claudia, Waghorn Katherine, Chase Andrew, Hehlmann Rüdiger, Reiter Andreas, Hochhaus Andreas, Cross Nicholas C P

机构信息

Wessex Regional Genetics Laboratory, University of Southampton, Salisbury, United Kingdom.

出版信息

Blood. 2007 Aug 15;110(4):1283-90. doi: 10.1182/blood-2007-02-074252. Epub 2007 Apr 24.

Abstract

Derivative chromosome 9 deletions are seen in 10% to 15% of patients with chronic myelogenous leukemia and have been associated with a poor prognosis; however, no studies have been performed in the context of a randomized clinical trial. We developed a DNA-based deletion screen and investigated 339 chronic phase patients treated with interferon-alpha as first-line therapy in 3 controlled German studies with a median observation time of 7 years. Deletions were detected in pretreatment DNA of 59 of 339 (17%) patients. Of these, 21 spanned the ABL/BCR junction and 38 were centromeric (n = 20) or telomeric (n = 18) of the breakpoint. There was no significant difference in overall survival between deleted and nondeleted patients. Patients with breakpoint-spanning deletions had poorer survival compared with patients without deletions (4.7 versus 7.8 years; P = .003), but this was not significant when censored at allogeneic stem cell transplantation (n = 129) or imatinib (n = 62) treatment in the first chronic phase (P = .078). Unexpectedly, deletions that did not span the breakpoint were associated with improved survival compared with cases without deletions (P = .001). Multiple Cox regression analysis indicated that deletion status (P = .007), age (P = .018), and spleen enlargement (P < .001) were significant independent indicators of survival and confirmed that only deletions spanning the ABL/BCR breakpoint were associated with an adverse prognosis (P = .039).

摘要

在10%至15%的慢性粒细胞白血病患者中可见衍生9号染色体缺失,且与预后不良相关;然而,尚未在随机临床试验背景下开展相关研究。我们开发了一种基于DNA的缺失筛查方法,并在3项德国对照研究中调查了339例接受α干扰素一线治疗的慢性期患者,中位观察时间为7年。在339例患者中的59例(17%)预处理DNA中检测到缺失。其中,21例缺失跨越ABL/BCR连接点,38例位于断点的着丝粒(n = 20)或端粒(n = 18)区域。缺失患者与未缺失患者的总生存期无显著差异。与未发生缺失的患者相比,断点跨越性缺失患者的生存期较差(4.7年对7.8年;P = 0.003),但在首个慢性期接受异基因干细胞移植(n = 129)或伊马替尼(n = 62)治疗时进行删失后,差异无统计学意义(P = 0.078)。出乎意料的是,与未发生缺失的病例相比,未跨越断点的缺失与生存期改善相关(P = 0.001)。多因素Cox回归分析表明,缺失状态(P = 0.007)、年龄(P = 0.018)和脾肿大(P < 0.001)是生存的显著独立指标,并证实只有跨越ABL/BCR断点的缺失与不良预后相关(P = 0.039)。

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