Department of Lymphoma and Myeloma, Institute of Hematology and Blood Diseases Hospital, State Key Laboratory of Experimental Hematology, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, People's Republic of China.
Leuk Lymphoma. 2013 Jan;54(1):123-32. doi: 10.3109/10428194.2012.704033. Epub 2012 Sep 5.
The serum free light chain (sFlc) levels were measured for 122 Chinese patients with newly diagnosed symptomatic multiple myeloma (NDSMM), and κ/λ ratios (rFlc) were calculated. The data were analyzed for the roles of sFlc and rFlc in the diagnosis and prognosis of MM. Abnormal sFlc and/or rFlc were detected in 99.2% of patients, demonstrating that the FLC assay is much more sensitive than the commonly used methods. Baseline sFlc and rFlc successfully predicted the overall survival (OS). The median OS was not reached (NR) versus 23 months for the low sFLC group (sFLC-κ < 180 mg/L or sFLC-λ < 592.5 mg/L) and high sFLC group (sFLC-κ ≥ 180 mg/L or sFLC-λ ≥ 592.5 mg/L) (p = 0.001), and NR versus 21 months for the low rFLC group (0.04 ≤ rFLC ≤ 25) and high rFLC group (p < 0.001), respectively. Interestingly, the significant differences in OS between the low and high rFLC groups were not changed by bortezomib chemotherapy. In addition, patients were further stratified by three novel poor-prognosis factors (β(2)-microglobulin [β2-MG] > 3.5 mg/L, albumin [ALB] < 35 g/L, rFLC > 25 or rFLC < 0.04) that were developed from combination of the rFlc with the International Staging System (ISS): the low risk group (no factor), the low-intermediate risk group (one factor), the high-intermediate risk group (two factors) and the high risk group (three factors). The median OS for those groups was NR, NR, 24 months and 13 months, respectively (p < 0.05). In conclusion, the sFLC assay was highly sensitive in the diagnosis of MM in Chinese patients. The prognostic potential of the ISS may be improved with the addition of rFLC.
对 122 例新诊断有症状多发性骨髓瘤(NDSMM)中国患者进行了血清游离轻链(sFlc)水平检测,并计算了κ/λ 比值(rFlc)。分析 sFlc 和 rFlc 在 MM 诊断和预后中的作用。99.2%的患者检测到异常 sFlc 和/或 rFlc,表明 FLC 检测比常用方法更敏感。基线 sFlc 和 rFlc 成功预测了总生存期(OS)。低 sFLC 组(sFLC-κ<180mg/L 或 sFLC-λ<592.5mg/L)和高 sFLC 组(sFLC-κ≥180mg/L 或 sFLC-λ≥592.5mg/L)的中位 OS 未达到(NR)分别为 23 个月(p=0.001),低 rFLC 组(0.04≤rFLC≤25)和高 rFLC 组(p<0.001)的中位 OS 分别为 NR 和 21 个月。有趣的是,低 rFLC 组和高 rFLC 组之间 OS 的显著差异在硼替佐米化疗后并未改变。此外,根据三个新的预后不良因素(β(2)-微球蛋白[β2-MG]>3.5mg/L、白蛋白[ALB]<35g/L、rFLC>25 或 rFLC<0.04)对患者进一步分层,这些因素是从 rFlc 与国际分期系统(ISS)的结合中得出的:低危组(无因素)、低中危组(一个因素)、高中危组(两个因素)和高危组(三个因素)。这些组的中位 OS 分别为 NR、NR、24 个月和 13 个月(p<0.05)。总之,sFlc 检测在中国患者 MM 的诊断中具有很高的灵敏度。ISS 的预后潜力可能通过添加 rFlc 得到改善。