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Prognostic value of the serum free light chain ratio in newly diagnosed myeloma: proposed incorporation into the international staging system

机译:血清游离轻链比率在新诊断的骨髓瘤中的预后价值:建议纳入国际分期系统

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摘要

To determine if the serum free light chain (FLC) ratio has prognostic value in patients with symptomatic multiple myeloma (MM), baseline serum samples from a well-characterized cohort of 790 newly diagnosed MM patients were tested with the FLC assay. FLC ratio was calculated as κ/λ (reference range 0.26–1.65). On the basis of the distribution of values, a cutpoint κ/λ FLC ratio of <0.03 or >32 was chosen for further analysis. Overall survival was significantly inferior in patients with an abnormal FLC ratio of <0.03 or >32 (n=479) compared with those with an FLC ratio between 0.03 and 32 (n=311), with median survival of 30 versus 39 months, respectively. We incorporated abnormal FLC ratio with the International Staging System (ISS) risk factors (that is, albumin <3.5 g/dl and serum β2-microglobulin ≥3.5 g/l), to create a risk stratification model with improved prognostic capabilities. Patients with 0, 1, 2 or 3 adverse risk factors had significantly different overall survival, with median survival times of 51, 39, 30 and 22 months, respectively (P<0.001). These findings suggest that the serum FLC ratio at initial diagnosis is an important predictor of prognosis in myeloma, and can be incorporated into the ISS for improved risk stratification.
机译:为了确定症状性多发性骨髓瘤(MM)患者的血清游离轻链(FLC)比率是否具有预后价值,使用FLC分析法测试了特征明确的790名新诊断MM患者队列中的基线血清样品。 FLC比值计算为κ/λ(参考范围0.26-1.65)。根据值的分布,选择了<0.03或> 32的临界点κ/λFLC比值进行进一步分析。 FLC比率<0.03或> 32(n = 479)的患者的总生存期显着低于FLC比率在0.03和32之间的患者(n = 311),中位生存期分别为30个月和39个月。我们将异常FLC比率与国际分期系统(ISS)风险因素(即白蛋白<3.5 g / dl和血清β2-微球蛋白≥3.5g / l)合并在一起,以建立具有改善的预后能力的风险分层模型。具有0、1、2或3个不利危险因素的患者的总生存期显着不同,中位生存时间分别为51、39、30和22个月(P <0.001)。这些发现表明,最初诊断时的血清FLC比率是骨髓瘤预后的重要预测指标,可以将其纳入ISS中以改善风险分层。

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