scholarly journals High-Dose Rituximab and Early Remission in PLA2R1-Related Membranous Nephropathy

2019 ◽  
Vol 14 (8) ◽  
pp. 1173-1182 ◽  
Author(s):  
Barbara Seitz-Polski ◽  
Karine Dahan ◽  
Hanna Debiec ◽  
Alexandra Rousseau ◽  
Marine Andreani ◽  
...  

Background and objectivesDifferent rituximab protocols are used to treat membranous nephropathy. We compared two rituximab protocols in patients with membranous nephropathy.Design, setting, participants, & measurementsTwenty-eight participants from the NICE cohort received two infusions of 1-g rituximab at 2-week intervals, whereas 27 participants from the Prospective Randomized Multicentric Open Label Study to Evaluate Rituximab Treatment for Membranous Nephropathy (GEMRITUX) cohort received two infusions of 375 mg/m2 at 1-week interval. We measured serum rituximab levels and compared remission at month 6 and before any treatment modification and analyzed factors associated with remission and relapses.ResultsRemissions occurred in 18 (64%) versus eight (30%) from the NICE and GEMRITUX cohort (P=0.02) at month 6, respectively, and in 24 (86%) versus 18 (67%) participants (P=0.12) before treatment modification, respectively. Median time to remission was 3 [interquartile range (IQR), 3–9] and 9 [IQR, 6–12] months for NICE and GEMRITUX cohorts respectively (P=0.01). Participants from the NICE cohort had higher circulating level of rituximab and lower CD19 counts (3.3 µg/L [IQR, 0.0–10.8] versus 0.0 [IQR, 0.0–0.0] P<0.001 and 0.0 [IQR, 0.0–2.0] versus 16.5 [IQR, 2.5–31.0] P<0.001) at month 3, lower level of anti-PLA2R1 antibodies at month 6 (0.0 [IQR, 0.0–8.0] versus 8.3 [IQR, 0.0–73.5] P=0.03). In the combined study population, lower epitope spreading at diagnosis and higher rituximab levels at month 3 were associated with remissions at month 6 (13/26 (50%) versus 22/29 (76%) P=0.05 and 2.2 µg/ml [IQR, 0.0–10.9] versus 0.0 µg/ml [IQR, 0.0–0.0] P<0.001 respectively). All non-spreaders entered into remission whatever the protocol. Eight of the 41 participants who reached remission had relapses. Epitope spreading at diagnosis (8/8 (100%) versus 16/33 (48%) P=0.01) and incomplete depletion of anti-PLA2R1 antibodies at month 6 (4/8 (50%) versus 5/33 (9%) P=0.05) were associated with relapses.ConclusionsOur work suggests that higher dose rituximab protocol is more effective on depletion of B-cells and lack of epitope spreading is associated with remission of membranous nephropathy.

2004 ◽  
Vol 42 (02) ◽  
pp. 98-102 ◽  
Author(s):  
D. Anderson ◽  
N. Kato ◽  
K. Onomichi ◽  
H. Uchida ◽  
S. Shelley ◽  
...  

2011 ◽  
Vol 38 (10) ◽  
pp. 2186-2192 ◽  
Author(s):  
YOSHIAKI FURUYA ◽  
MASATAKA KUWANA

Objective.To evaluate the clinical benefits of the endothelin receptor antagonist bosentan on interstitial lung disease (ILD) in patients with systemic sclerosis (SSc) who are ineligible for cyclophosphamide (CYC) therapy.Methods.In this prospective open-label study, 9 patients with SSc and ILD received bosentan for 24 months. The main reasons for avoiding CYC included severely impaired lung function, long disease duration, and relapse after CYC treatment. Pulmonary function tests and Doppler echocardiograms were evaluated every 6 months, and high-resolution computed tomography (HRCT) was performed every 12 months. For an extended survival analysis, 17 historical controls who met the inclusion criteria at referral and had not used any immunosuppressive or antifibrotic agents thereafter were selected from the SSc database.Results.Two patients did not finish the study; one developed vasculitis requiring high-dose corticosteroids and another died of bacterial pneumonia. The remaining 7 patients tolerated bosentan and completed the study period. There were trends toward mildly reduced forced vital capacity, total lung capacity, and diffusing capacity for carbon monoxide over time. Two patients developed pulmonary hypertension during the 24-month period. HRCT scores for ground-glass opacity, pulmonary fibrosis, and honeycomb cysts gradually increased. In the extended study, there was no difference in cumulative survival rate between the bosentan-treated and historical control groups.Conclusion.The gradual worsening of pulmonary function and HRCT findings in patients treated with bosentan was consistent with the natural course of SSc-associated ILD. This study does not support the use of bosentan for SSc-associated ILD even when CYC treatment is inadvisable.


1996 ◽  
Vol 19 (4) ◽  
pp. 341-348 ◽  
Author(s):  
Richard B. Rosse ◽  
Kathie Kendrick ◽  
Maureen Fay-McCarthy ◽  
George D. Prell ◽  
Paul Rosenberg ◽  
...  

1995 ◽  
Vol 15 (1-2) ◽  
pp. 148
Author(s):  
Richard B. Rosse ◽  
Kathleen A. Kendrick ◽  
Maureen Fay-McCarthy ◽  
Joseph P. Collins ◽  
Paul B. Rosenberg ◽  
...  

2017 ◽  
Vol 27 ◽  
pp. S861 ◽  
Author(s):  
S.H. Horikoshi ◽  
I.M. Miura ◽  
S.Y. Yamamoto ◽  
O.A. Abe ◽  
M.I. Ito ◽  
...  

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