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Incidence of hypogammaglobulinemia in patients receiving rituximab and the use of intravenous immunoglobulin for recurrent infections

机译:接受利妥昔单抗的患者发生低血球蛋白血症的发生率,以及静脉注射免疫球蛋白用于复发性感染

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摘要

Background: Rituximab has altered the treatment approach to B-cell malignancies and other diseases. Reports consider that rituximab had limited impact on serum immunoglobulins. However, anecdotes suggest that rituximab can cause symptomatic hypogammaglobulinemia. This retrospective study examined the relationship among rituximab, hypogammaglobulinemia, and treatment of symptomatic hypogammaglobulinemia with intravenous immune globulin (IVIG). Methods: Patients with serial quantitative serum immunoglobulin (SIgG) concentrations before and subsequent to rituximab administration at Memorial Sloan-Kettering Cancer Center were identified. Information regarding rituximab administration, SIgG concentrations, frequency of infection, and administration of IVIG were recorded. Results: Between December 1998 and April 2009, 211 patients with B-cell lymphoma treated with rituximab and with serial SIgG concentrations were identified. One hundred seventy-nine (85%) patients had normal SIgG before rituximab, 32 (15%) had low SIgG. After rituximab use, hypogammaglobulinemia was identified in 38.54% of patients with initially normal SIgG. The risk was greater in patients who received maintenance rituximab. Symptomatic hypogammaglobulinemia that prompted IVIG administration developed in 6.6% of patients. Conclusions: In this data set, rituximab administration was associated with a high frequency of hypogammaglobulinemia, particularly symptomatic hypogammaglobulinemia, among patients who received multiple courses of rituximab. Baseline and periodic monitoring of SIgGs is appropriate in patients who receive rituximab.
机译:背景:利妥昔单抗改变了B细胞恶性肿瘤和其他疾病的治疗方法。报告认为利妥昔单抗对血清免疫球蛋白的影响有限。然而,轶事表明利妥昔单抗可引起症状性低血球蛋白血症。这项回顾性研究探讨了利妥昔单抗,低球蛋白球蛋白血症和有症状的低球蛋白球蛋白血症合并静脉注射免疫球蛋白(IVIG)的关系。方法:确定在纪念斯隆-凯特琳癌症中心接受利妥昔单抗治疗前后有连续定量血清免疫球蛋白(SIgG)浓度的患者。记录有关利妥昔单抗给药,SIgG浓度,感染频率和IVIG给药的信息。结果:在1998年12月至2009年4月之间,确定了211例接受利妥昔单抗治疗并伴有一系列SIgG浓度的B细胞淋巴瘤患者。 179名(85%)患者在利妥昔单抗之前SIgG正常,32名(15%)患者SIgG较低。使用利妥昔单抗后,在38.54%最初SIgG正常的患者中发现了低丙种球蛋白血症。接受维持性利妥昔单抗治疗的患者的风险更大。 6.6%的患者发生了提示IVIG给药的症状性低丙种球蛋白血症。结论:在该数据集中,接受多疗程利妥昔单抗的患者中,利妥昔单抗的给药与高频率的低球蛋白球蛋白血症,尤其是有症状的低球蛋白球蛋白血症相关。对接受利妥昔单抗的患者进行SIgG的基线和定期监测是合适的。

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