Inoki Yuta, Nishi Kentaro, Sato Mai, Ogura Masao, Kamei Koichi
Division of Nephrology and Rheumatology, National Center for Child Health and Development, 2-10-1, Okura, Setagaya-ku, Tokyo, 157-853, Japan.
Pediatr Nephrol. 2023 Feb;38(2):451-460. doi: 10.1007/s00467-022-05652-9. Epub 2022 Jun 24.
Hypogammaglobulinemia is a major adverse effect from rituximab. However, the association between rituximab-induced hypogammaglobulinemia and infection frequency is unknown.
Patients who received rituximab for complicated nephrotic syndrome between February 2006 and October 2020 were enrolled in this retrospective observational study. Infections requiring antibacterial or antiviral agents or hospitalization were identified, and the characteristics of infections were compared according to infection type.
One hundred and forty patients were enrolled. Fifty infection events were detected in 36 patients, 45 infection events in 32 patients required hospitalization, and 1 severe infection event required intensive care unit admission. In eight patients who developed severe hypogammaglobulinemia (serum IgG level < 200 mg/dL) for more than 1 year after rituximab treatment, eight infections occurred in six patients; six of these infections did not occur during the period of severe hypogammaglobulinemia. Febrile neutropenia accounted for 54.2% (13/24) of all infections among the patients with hypogammaglobulinemia. The incidence of infections was 0.028 (95% confidence interval = 0.017-0.448), 0.071 (95% [CI] = 0.041-0.114), and 0.096 (95% [CI] = 0.019-0.282) patient-years in patients with normal serum IgG levels and those with mild and severe hypogammaglobulinemia, respectively. Immunoglobulin replacement therapy was not administered to any patients except for the treatment of infection.
Our results showed no statistically significant association between hypogammaglobulinemia severity and infection rate. In addition, the frequency of infection was relatively low even in patients with severe hypogammaglobulinemia, suggesting that immunoglobulin replacement therapy may not be necessary for rituximab-treated patients with severe hypogammaglobulinemia. A higher resolution version of the Graphical abstract is available as Supplementary information.
低丙种球蛋白血症是利妥昔单抗的主要不良反应。然而,利妥昔单抗诱导的低丙种球蛋白血症与感染频率之间的关联尚不清楚。
本回顾性观察研究纳入了2006年2月至2020年10月期间因复杂性肾病综合征接受利妥昔单抗治疗的患者。确定需要使用抗菌或抗病毒药物或住院治疗的感染情况,并根据感染类型比较感染特征。
共纳入140例患者。36例患者发生了50次感染事件,32例患者的45次感染事件需要住院治疗,1例严重感染事件需要入住重症监护病房。在利妥昔单抗治疗后出现严重低丙种球蛋白血症(血清IgG水平<200mg/dL)超过1年的8例患者中,6例患者发生了8次感染;其中6次感染并非发生在严重低丙种球蛋白血症期间。发热性中性粒细胞减少症占低丙种球蛋白血症患者所有感染的54.2%(13/24)。血清IgG水平正常、轻度和重度低丙种球蛋白血症患者的感染发生率分别为0.028(95%置信区间=0.017-0.448)、0.071(95%[CI]=0.041-0.114)和0.096(95%[CI]=0.019-0.282)患者-年。除治疗感染外,未对任何患者进行免疫球蛋白替代治疗。
我们的结果显示低丙种球蛋白血症严重程度与感染率之间无统计学显著关联。此外,即使是严重低丙种球蛋白血症患者,感染频率也相对较低,这表明对于接受利妥昔单抗治疗的严重低丙种球蛋白血症患者,可能无需进行免疫球蛋白替代治疗。更高分辨率的图形摘要版本可作为补充信息获取。