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[Long-term efficacy of low-dose rituximab treatment in patients with primary membranous nephropathy].
Qi, Y; Jia, J Y; Gu, Q H; Zheng, Z F; Li, L N; Li, D; Jia, Z H; Xue, Y; Yan, T K.
Afiliação
  • Qi Y; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Jia JY; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Gu QH; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Zheng ZF; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Li LN; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Li D; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Jia ZH; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Xue Y; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
  • Yan TK; Department of Nephrology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Zhonghua Yi Xue Za Zhi ; 102(40): 3201-3206, 2022 Nov 01.
Article em Zh | MEDLINE | ID: mdl-36319174
Objective: To explore the long-term efficacy of low-dose rituximab (RTX) treatment in patients with primary membranous nephropathy (PMN). Methods: Patients with biopsy-proven PMN who received low-dose RTX as initial or second-line regimen from August 2018 to May 2020 in the Department of Nephrology, Tianjin Medical University General Hospital were respectively enrolled. The clinical parameters of patients were urinary protein>3.5 g/24 h, serum albumin<30 g/L and estimated glomerular filtration rate (eGFR)>20 ml·min-1·(1.73 m2)-1. The treatment response of patients with PMN was observed during follow-up, and the remission rate of patients with urinary protein<8 g/24 h or ≥8 g/24 h, anti-PLA2R antibody<150 RU/ml or ≥150 RU/ml, eGFR≥ 60 ml·min-1·(1.73 m2)-1 or<60 ml·min-1·(1.73 m2)-1 were analyzed, respectively. Results: A total of 40 patients were enrolled, including 26 males and 14 females, aged (53±15) years. There were 14 patients received RTX as initial treatment and 26 patients as second-line therapy. The total median dose of RTX in the first course was 800 (425, 1 075) mg. The overall remission rate at the 1st, 3rd, 6th, 12th and 24th months were 12.5% (5/40), 17.5% (7/40), 47.5% (19/40), 57.5% (23/40), 60% (24/40), respectively. The median overall response time was 6.0 (3.0, 7.5) months. Two cases relapsed. Patients with remission (n=24) had a higher level of baseline eGFR [(93.9±28.0) vs (62.4±28.1) ml·min-1·(1.73 m2)-1, P=0.001), and a lower level of both urinary protein [5.9 (5.0, 6.5) vs 11.7 (8.6, 15.5) g/24 h, P<0.001] and anti-PLA2R antibody level [73 (29, 132) vs 453 (182, 950) RU/ml, P=0.004] than those without remission (n=16) 24 month after treatment. There was no statistically significant difference in the remission rate between initial and second-line treatment (P=0.101). Moreover, patients had a higher remission rate in urinary protein<8 g/24 h group (21/26 vs 3/14, P<0.001), anti-PLA2R antibody<150 RU/ml group (16/19 vs 5/16, P=0.002) and eGFR ≥ 60 ml·min-1·(1.73 m2)-1 group (22/29 vs 2/11, P=0.003). Conclusions: Low-dose RTX treatment in PMN is effective during long-term follow-up, and has a lower recurrence rate. The results also suggest that it is more suitable for patients with baseline urinary protein<8 g/24 h, anti-PLA2R antibody<150 RU/ml and eGFR≥ 60 ml·min-1·(1.73 m2)-1.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Glomerulonefrite Membranosa Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: Zh Revista: Zhonghua Yi Xue Za Zhi Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Glomerulonefrite Membranosa Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: Zh Revista: Zhonghua Yi Xue Za Zhi Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China