首页> 外文期刊>Acta Haematologica >Clinical value of absolute lymphocyte counts before bortezomib-dexamethasone therapy in relapsed multiple myeloma patients.
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Clinical value of absolute lymphocyte counts before bortezomib-dexamethasone therapy in relapsed multiple myeloma patients.

机译:硼替佐米-地塞米松治疗前复发性多发性骨髓瘤患者绝对淋巴细胞计数的临床价值。

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A high absolute lymphocyte count (ALC) at diagnosis is known as a surrogate marker of favorable prognosis in newly diagnosed multiple myeloma (MM). Recent studies showed tumor sensitization and enhanced cytotoxicity of bortezomib. We hypothesized that a high ALC before bortezomib treatment would contribute to tumor sensitization and activated cytotoxicity of bortezomib in relapsed MM. Ninety-seven relapsed MM patients who underwent bortezomib-dexamethasone (Vel-Dex) therapy were analyzed. Median follow-up duration was 21 months and median age was 61 years. Complete response (CR) and very good partial response (VGPR) after 2 cycles of Vel-Dex therapy were higher in the high-ALC group (>or=1.1 x 10(9)/l) (CR + VGPR 50.0% in the high-ALC group vs. 10.4% in the low-ALC group, p = 0.001), and stable disease (SD) rate was lower in the high-ALC group (SD 11.8% in the high-ALC group vs. 44.8% in the low-ALC group, p < 0.001). In the univariate analysis, the low-ALC group before therapy was associated with shorter progression-free survival (PFS) [hazard ratio (HR), 2.780; 95% confidence interval (95% CI) 1.703-4.536, p < 0.001]. Multivariate analysis revealed that a low ALC represented an independent predictive factor for PFS (HR 1.937, 95% CI 1.168-3.212, p = 0.010). A low ALC just before Vel-Dex therapy was associated with a poor prognosis in relapsed MM.
机译:诊断时高的绝对淋巴细胞计数(ALC)被认为是新诊断的多发性骨髓瘤(MM)预后良好的替代指标。最近的研究显示了硼替佐米的肿瘤敏感性和增强的细胞毒性。我们假设在硼替佐米治疗之前较高的ALC将有助于复发性MM中的肿瘤敏感性和硼替佐米的活化细胞毒性。分析了接受硼替佐米-地塞米松(Vel-Dex)治疗的97例复发MM患者。中位随访时间为21个月,中位年龄为61岁。高ALC组在2个周期的Vel-Dex治疗后的完全缓解(CR)和非常好的部分缓解(VGPR)较高(>或= 1.1 x 10(9)/ l)(CR + VGPR为50.0%高ALC组比低ALC组的10.4%,p = 0.001),高ALC组的稳定疾病(SD)发生率较低(高ALC组的SD 11.8%,高ALC组的44.8%低ALC组,p <0.001)。在单因素分析中,治疗前的低ALC组与较短的无进展生存期(PFS)相关[危险比(HR)为2.780; 95%置信区间(95%CI)1.703-4.536,p <0.001]。多变量分析显示,低ALC代表PFS的独立预测因素(HR 1.937,95%CI 1.168-3.212,p = 0.010)。 Vel-Dex治疗之前的低ALC与复发性MM预后不良有关。

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