Department of Nephrology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Assistance Publique des Hôpitaux de Paris, Service de Néphrologie et Transplantation, Hôpital Universitaire Necker-Enfants Malades, Université de Paris, Paris, France.
Am J Transplant. 2021 Sep;21(9):3021-3033. doi: 10.1111/ajt.16504. Epub 2021 Feb 23.
Rituximab (RTX) therapy for primary focal segmental glomerulosclerosis recurrence after kidney transplantation (KT) has been extensively debated. We aimed to assess the benefit of adding RTX to plasmapheresis (PP), corticosteroids, and calcineurin inhibitors (standard of care, SOC). We identified 148 adult patients who received KT in 12/2004-12/2018 at 21 French centers: 109 received SOC (Group 1, G1), and 39 received immediate RTX along with SOC (Group 2, G2). In G1, RTX was introduced after 28 days of SOC in the event of failure (G1a, n = 19) or PP withdrawal (G1b, n = 12). Complete remission (CR) was achieved in 46.6% of patients, and partial remission (PR) was achieved in 33.1%. The 10-year graft survival rates were 64.7% and 17.9% in responders and nonresponders, respectively. Propensity score analysis showed no difference in CR+PR rates between G1 (82.6%) and G2 (71.8%) (p = .08). Following the addition of RTX (G1a), 26.3% of patients had CR, and 31.6% had PR. The incidence of severe infections was similar between patients treated with and without RTX. In multivariable analysis, infection episodes were associated with hypogammaglobulinemia <5 g/L. RTX could be used in cases of SOC failure or remission for early discontinuation of PP without increasing the risk of infection.
利妥昔单抗(RTX)治疗肾移植(KT)后原发性局灶节段性肾小球硬化(FSGS)复发已广泛讨论。我们旨在评估将 RTX 与血浆置换(PP)、皮质类固醇和钙调磷酸酶抑制剂(标准治疗,SOC)联合使用的益处。我们在 21 个法国中心确定了 148 名在 2004 年 12 月至 2018 年 12 月期间接受 KT 的成年患者:109 名患者接受 SOC(G1 组),39 名患者在 SOC 时立即接受 RTX(G2 组)。在 G1 组中,SOC 失败(G1a,n=19)或 PP 停药(G1b,n=12)后 28 天引入 RTX。46.6%的患者获得完全缓解(CR),33.1%的患者获得部分缓解(PR)。应答者和无应答者的 10 年移植物存活率分别为 64.7%和 17.9%。倾向评分分析显示 G1(82.6%)和 G2(71.8%)之间 CR+PR 率无差异(p=0.08)。在添加 RTX(G1a)后,26.3%的患者获得 CR,31.6%的患者获得 PR。接受和未接受 RTX 治疗的患者严重感染的发生率相似。多变量分析显示,感染发作与 <5 g/L 的低丙种球蛋白血症有关。SOC 失败或缓解时 RTX 可用于早期停用 PP,而不会增加感染风险。