Gao Shuang, Cui Zhao, Wang Xin, Zhang Yi-Miao, Wang Fang, Cheng Xu-Yang, Meng Li-Qiang, Zhou Fu-de, Liu Gang, Zhao Ming-Hui
Renal Division, Peking University First Hospital, Beijing, China.
Institute of Nephrology, Peking University, Beijing, China.
Front Med (Lausanne). 2021 May 20;8:663680. doi: 10.3389/fmed.2021.663680. eCollection 2021.
Rituximab has become one of the first-line therapies for the treatment of moderate and high-risk primary membranous nephropathy (pMN). We retrospectively reviewed 95 patients with pMN who received rituximab therapy and focused on the therapeutic effects and safety of this therapy in a Chinese cohort. Ninety-five consecutive patients with pMN diagnosed by kidney biopsy received rituximab and were followed up for >6 months. Four weekly doses of rituximab (375 mg/m) was adopted as the initial administration. Repeated single infusions were administrated to maintain B cell depletion levels of <5 cells/mL. A total of 91 patients completed rituximab therapy with the total dose of 2.4 (2.0, 3.0) g; 64/78 (82.1%) patients achieved anti-PLA2R antibody depletion in 6.0 (1.0, 12.0) months; 53/91 (58.2%) patients achieved clinical remission in 12.0 (6.0, 24.0) months, including complete remission in 18.7% of patients and partial remission in 39.6% of patients. Multivariate logistic regression analysis showed that severe proteinuria (OR = 1.22, = 0.006) and the persistent positivity of anti-PLA2R antibodies (OR = 9.00, = 0.002) were independent risk factors for no-remission. The remission rate of rituximab as an initial therapy was higher than rituximab as an alternative therapy (73.1 vs. 52.3%, = 0.038). Lastly, 45 adverse events occurred in 37 patients, but only one patient withdrew from treatment due to severe pulmonary infection. Rituximab is a safe and effective treatment option for Chinese patients with pMN, especially as an initial therapy.
利妥昔单抗已成为治疗中高危原发性膜性肾病(pMN)的一线疗法之一。我们回顾性分析了95例接受利妥昔单抗治疗的pMN患者,重点关注该疗法在中国人群中的治疗效果和安全性。95例经肾活检确诊的连续性pMN患者接受了利妥昔单抗治疗,并进行了超过6个月的随访。初始给药采用每周4次剂量的利妥昔单抗(375 mg/m²)。重复单次输注以维持B细胞耗竭水平<5个细胞/mL。共有91例患者完成利妥昔单抗治疗,总剂量为2.4(2.0,3.0)g;64/78(82.1%)例患者在6.0(1.0,12.0)个月时抗PLA2R抗体耗竭;53/91(58.2%)例患者在12.0(6.0,24.0)个月时达到临床缓解,其中18.7%的患者完全缓解,39.6%的患者部分缓解。多因素logistic回归分析显示,重度蛋白尿(OR = 1.22,P = 0.006)和抗PLA2R抗体持续阳性(OR = 9.00,P = 0.002)是未缓解的独立危险因素。利妥昔单抗作为初始治疗的缓解率高于作为替代治疗的缓解率(73.1%对52.3%,P = 0.038)。最后,37例患者发生了45次不良事件,但仅有1例患者因严重肺部感染退出治疗。利妥昔单抗对于中国pMN患者是一种安全有效的治疗选择,尤其是作为初始治疗。