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免疫球蛋白重链可变区突变状态在 del(13q)慢性淋巴细胞白血病中的重要性。

Importance of immunoglobulin heavy chain variable region mutational status in del(13q) chronic lymphocytic leukemia.

机构信息

The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD 21287, USA.

出版信息

Leuk Lymphoma. 2011 Oct;52(10):1873-81. doi: 10.3109/10428194.2011.585529. Epub 2011 Aug 18.

Abstract

Among prognostic factors for chronic lymphocytic leukemia (CLL), immunoglobulin heavy chain variable region (IGHV) mutation status and DNA analysis appear to be the most important. However, there is limited clinical outcome information for patients with the favorable-risk del(13q) and poor-risk unmutated IGHV. We retrospectively screened all patients with CLL at our institution between 2004 and June 2010 for del(13q) who also had an IGHV analysis. Unmutated IGHV was found in 38/79 patients; age, Rai stage, prior therapy, and time to evaluation were similar to those for patients with mutated IGHV. Unmutated patients were nearly four times more likely to harbor additional chromosomal aberrations compared to mutated patients (p < 0.001). During a median follow-up of 4.5 years, unmutated patients were more likely to demonstrate Rai stage progression (69% vs. 31%, log-rank p < 0.001) and to receive treatment (5-year cumulative probability of treatment: 65% vs. 32%, p < 0.001). Patients with unmutated CLL also had a shorter overall survival (5-year survival probability: 72% vs. 100%, p < 0.001). When limiting analysis to the 47 patients with del(13q) as a sole chromosomal abnormality, the 13 (28%) unmutated patients were more likely to demonstrate Rai progression (p < 0.001), to receive treatment (p = 0.02), and to have a shorter overall survival (p = 0.13) than the 34 mutated patients. These data suggest that del(13q) conveys an indolent course only in patients with IGHV-mutated CLL.

摘要

在慢性淋巴细胞白血病 (CLL) 的预后因素中,免疫球蛋白重链可变区 (IGHV) 突变状态和 DNA 分析似乎最为重要。然而,对于具有有利风险的 del(13q)和不良风险的未突变 IGHV 的患者,其临床结果信息有限。我们回顾性筛选了 2004 年至 2010 年 6 月期间在我们机构就诊的所有 CLL 患者,这些患者均存在 del(13q)且IGHV 也有分析。在 79 例患者中发现了 38 例未突变的 IGHV;年龄、Rai 分期、既往治疗和评估时间与 IGHV 突变患者相似。与突变患者相比,未突变患者更有可能存在额外的染色体异常(p<0.001)。在中位随访 4.5 年期间,未突变患者更有可能出现 Rai 分期进展(69%比 31%,对数秩检验 p<0.001),且更有可能接受治疗(5 年累积治疗概率:65%比 32%,p<0.001)。未突变的 CLL 患者的总生存时间也较短(5 年生存率:72%比 100%,p<0.001)。当将分析仅限于作为唯一染色体异常的 47 例 del(13q)患者时,13 例(28%)未突变患者更有可能出现 Rai 进展(p<0.001),更有可能接受治疗(p=0.02),且总生存时间更短(p=0.13),而 34 例突变患者则没有。这些数据表明,del(13q)仅在 IGHV 突变的 CLL 患者中传递惰性病程。

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