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异常的血清游离轻链比值与生存期较差相关,且可能反映慢性淋巴细胞白血病患者的生物学亚组。

Abnormal serum free light chain ratios are associated with poor survival and may reflect biological subgroups in patients with chronic lymphocytic leukaemia.

作者信息

Pratt Guy, Harding Stephen, Holder Roger, Fegan Chris, Pepper Chris, Oscier David, Gardiner Anne, Bradwell Arthur R, Mead Graham

机构信息

CRUK Institute for Cancer Studies, University of Birmingham, Birmingham, UK.

出版信息

Br J Haematol. 2009 Jan;144(2):217-22. doi: 10.1111/j.1365-2141.2008.07456.x. Epub 2008 Nov 11.

Abstract

The measurement of immunoglobulin serum free light chains (sFLC) has prognostic significance in plasma cell dyscrasias but its role in chronic lymphocytic leukaemia (CLL) is unknown. This retrospective study from three UK hospitals analysed sFLC in 181 untreated/pre-treatment CLL patients and 78 treated CLL patients, with samples taken later in their disease. An abnormal sFLC ratio was significantly associated with poor overall survival for the 181 untreated/pre-treatment patients (P = 0.0001) and for all patients (P = 0.002), irrespective of cause of death. Using multivariate analysis (n = 194), four independent prognostic variables for overall survival were identified namely Zap-70 (P = 0.0001), beta2M (P = 0.01), IGHV mutation status (P = 0.017) and an abnormal sFLC ratio (P = 0.024). For CLL patients with unmutated IGHV genes, elevated kappa/lambda ratios were adversely prognostic. For patients with mutated IGHV genes, reduced kappa/lambda ratios were adversely prognostic and associated with the poor prognostic IGHV3-21, IGHV3-48 and IGHV3-53 subgroups, suggesting an abnormal sFLC ratio may reflect biological subgroups within CLL. Abnormal sFLC ratios need to be studied prospectively in CLL patients and the biological rationale for their abnormality investigated.

摘要

免疫球蛋白血清游离轻链(sFLC)的检测在浆细胞异常增殖性疾病中具有预后意义,但其在慢性淋巴细胞白血病(CLL)中的作用尚不清楚。这项来自英国三家医院的回顾性研究分析了181例未经治疗/治疗前的CLL患者和78例接受治疗的CLL患者的sFLC,样本取自疾病后期。对于181例未经治疗/治疗前的患者(P = 0.0001)和所有患者(P = 0.002),异常的sFLC比值与总体生存率差显著相关,无论死亡原因如何。使用多变量分析(n = 194),确定了四个总体生存的独立预后变量,即Zap-70(P = 0.0001)、β2M(P = 0.01)、IGHV突变状态(P = 0.017)和异常的sFLC比值(P = 0.024)。对于IGHV基因未突变的CLL患者,κ/λ比值升高预后不良。对于IGHV基因发生突变的患者,κ/λ比值降低预后不良,并与预后不良的IGHV3-21、IGHV3-48和IGHV3-53亚组相关,提示异常的sFLC比值可能反映了CLL中的生物学亚组。需要对CLL患者进行前瞻性研究sFLC比值异常情况,并研究其异常的生物学原理。

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