C5a receptor inhibitor avacopan in immunoglobulin A nephropathy-an open-label pilot study

被引:72
作者
Bruchfeld, Annette [1 ,2 ,3 ]
Magin, Hasan [2 ,3 ]
Nachman, Patrick [4 ]
Parikh, Samir [5 ]
Lafayette, Richard [6 ]
Potarca, Antonia [7 ]
Miao, Shichang [7 ]
Bekker, Pirow [7 ]
机构
[1] Linkoping Univ, Dept Hlth Med & Caring Sci, Linkoping, Sweden
[2] Karolinska Univ Hosp, Dept Renal Med, Stockholm, Sweden
[3] Karolinska Inst, CLINTEC, Stockholm, Sweden
[4] Univ Minnesota, Div Renal Dis & Hypertens, Minneapolis, MN USA
[5] Ohio State Univ, Dept Nephrol, Wexner Med Ctr, Columbus, OH 43210 USA
[6] Stanford Univ, Dept Nephrol, Palo Alto, CA 94304 USA
[7] ChemoCentryx, San Carlos, CA USA
关键词
avacopan; C5a receptor; C5a receptor inhibitor; complement; IgA nephropathy; proteinuria; IGA NEPHROPATHY; CORTICOSTEROIDS;
D O I
10.1093/ckj/sfab294
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Improvement of proteinuria as a marker for disease activity is associated with a better renal outcome in immunoglobulin A nephropathy (IgAN). Complement is an effector pathway in IgA-mediated kidney injury. Avacopan, a selective C5a receptor inhibitor, has previously shown efficacy in anti-neutrophil cytoplasmic antibody-associated vasculitis. The aim of this study was to evaluate the safety and efficacy of avacopan in patients with IgAN with persistent proteinuria despite a maximally tolerated dose of renin-angiotensin-aldosterone system blockade. The efficacy evaluation was based on the change in proteinuria. Methods This open-label pilot trial enrolled adult patients with biopsy-proven IgAN, urinary protein:creatinine ratio (UPCR) >1 g/g creatinine and an estimated glomerular filtration rate (eGFR) >60 mL/min/1.73 m(2) or >45 mL/min/1.73 m(2) if eGFR has not declined >10 mL/min/1.73 m(2) over the previous 24 weeks. If the UPCR remained at >1 g/g creatinine after an 8-week run-in period, patients started avacopan 30 mg twice daily. The primary efficacy endpoint was the change in the slope of the UPCR from the 8-week run-in period to the slope in the 12-week avacopan dosing period. Results A total of 10 of 15 screened patients entered the run-in period. Seven patients with a UPCR >1 g/g creatinine received avacopan. Six of seven patients had numerical improvement in the UPCR during the avacopan treatment period, three of whom had a numerical improvement of similar to 50% at week 12. At week 24, five of seven patients still showed numerical improvement in the UPCR compared with baseline. The urinary monocyte chemoattractant protein-1:creatinine ratio decreased numerically 30% by week 8, possibly reflecting the anti-inflammatory activity of avacopan. Avacopan was well tolerated. There was one serious adverse event of unstable angina, which was deemed to be unrelated to avacopan. Conclusions This short-term pilot study showed an improvement in the slope of the UPCR, with similar to 50% improvement in three of seven patients with IgAN. Longer avacopan treatment duration may be indicated for maximal benefit.
引用
收藏
页码:922 / 928
页数:7
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