Department of Hematology and INSERM U918, IRIB, Centre Henri Becquerel, Rouen, France.
Leuk Lymphoma. 2013 Sep;54(9):1898-907. doi: 10.3109/10428194.2013.767456. Epub 2013 Feb 18.
Elevated serum free light chains (FLCs) have been associated with an unfavorable prognosis in diffuse large B-cell lymphoma (DLBCL). The aim of this study was to determine the clinical relevance of a quantitative assessment of intact circulating immunoglobulin (Ig), using serum Ig heavy chain/light chain pair (HLC) measurements in patients with DLBCL. FLC and HLC were measured in 409 serum samples of patients with DLBCL included in the LNH03-B clinical trial program of the Groupe d'Etudes des Lymphomes de l'Adulte (GELA). Patients with an abnormal IgMκ/IgMλ ratio or an abnormal FLC ratio more frequently displayed adverse clinical characteristics. Patients with abnormal IgMκ/IgMλ ratios had inferior progression-free survival (PFS) and overall survival (OS) as compared to patients with a normal ratio in the overall cohort (5-year PFS 44.9% vs. 69.3%, p = 0.0003 and 5-year OS 50.8% vs. 78.1%, p = 0.0003) and in the R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) cohort (5-year OS 43.5% vs. 70.3%, p = 0.003). In multivariate analysis, including elevated FLC/HLC and International Prognostic Index (IPI), an abnormal IgMκ/IgMλ ratio (hazard ratio [HR] = 1.54, 95% confidence interval [CI] 1.03-2.3, p = 0.03) remained predictive of shorter progression-free survival. Gene expression profile experiments and immunohistochemistry indicate that this measurement is at least partially related to tumor cell secretion. Both elevated serum FLCs and an abnormal IgMκ/IgMλ ratio are associated with unfavorable outcomes in patients with DLBCL treated by R-CHOP.
血清游离轻链(FLC)升高与弥漫性大 B 细胞淋巴瘤(DLBCL)的不良预后相关。本研究旨在通过测定血清免疫球蛋白重链/轻链对(HLC)来确定定量评估完整循环免疫球蛋白(Ig)在 DLBCL 患者中的临床相关性。在 Groupe d'Etudes des Lymphomes de l'Adulte(GELA)的 LNH03-B 临床试验方案中,对 409 例 DLBCL 患者的血清样本进行了 FLC 和 HLC 检测。IgMκ/IgMλ 比值异常或 FLC 比值异常的患者更常表现出不良的临床特征。在整个队列中,与比值正常的患者相比,IgMκ/IgMλ 比值异常的患者无进展生存期(PFS)和总生存期(OS)更差(5 年 PFS 44.9% vs. 69.3%,p = 0.0003 和 5 年 OS 50.8% vs. 78.1%,p = 0.0003),在 R-CHOP(利妥昔单抗、环磷酰胺、多柔比星、长春新碱、泼尼松)队列中(5 年 OS 43.5% vs. 70.3%,p = 0.003)。在包括升高的 FLC/HLC 和国际预后指数(IPI)的多变量分析中,异常的 IgMκ/IgMλ 比值(风险比 [HR] = 1.54,95%置信区间 [CI] 1.03-2.3,p = 0.03)仍然是无进展生存期较短的预测因素。基因表达谱实验和免疫组化表明,该测定至少部分与肿瘤细胞分泌有关。在接受 R-CHOP 治疗的 DLBCL 患者中,血清 FLC 升高和 IgMκ/IgMλ 比值异常均与不良预后相关。