Title: Plasma Exchange and Glucocorticoids in Severe ANCA-Associated Vasculitis
Author: Michael Walsh, M.D., Ph.D.,, Peter A. Merkel, M.D., M.P.H.,, Chen-Au Peh, F.R.A.C.P., Ph.D.,, Wladimir M. Szpirt, M.D.,, Xavier Puéchal, M.D., Ph.D.,, Shouichi Fujimoto, M.D., Ph.D.,, Carmel M. Hawley, M.B., B.S., M.Med.Sci.,, Nader Khalidi, M.D.,, Oliver Flomann, F.R.C.P., M.D.(Res),, Ron Wald, M.D.C.M., M.P.H.,, Louis P. Girard, M.D., M.B.T.,, Adeera Levin, M.D.,, Gina Gregorini, M.D.,, Lorraine Harper, F.R.C.P., Ph.D.,, William F. Clark, M.D.,, Christian Pagnoux, M.D., M.P.H.,, Ulrich Specks, M.D.,, Lucy Smyth, M.B., B.S.,, Vladimir Tesar, M.D., Ph.D.,, Toshiko Ito-Ihara, M.D., Ph.D.,, Janak Rashme de Zoysa, M.B., Ch.B.,, Wojciech Szczeklik, M.D., Ph.D.,, Luis Felipe Flores-Suárez, M.D., Ph.D.,, Simon Carette, M.D.,, Loc Guillevin, M.D.,, Charles D. Pusey, F.Med.Sci.,, Alina L. Casian, M.D.,, Biljana Brezina, M.Sc.,, Andrea Mazzetti, B.A.,, Carol A. McAlear, M.A.,, Elizabeth Broadhurst, B.Sc.,, Donna Reidlinger, M.P.H.,, Samir Mehta, M.Sc.,, Natalie Ives, M.Sc.,, and David R.W. Jayne, M.D.
More effective and safer treatments are needed for antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis.
We conducted a randomized trial with a 2-by-2 factorial design to evaluate the use of plasma exchange and two regimens of oral glucocorticoids in patients with severe ANCA-associated vasculitis (defined by an estimated glomerular filtration rate of <50 ml per minute per 1.73 m2 of body-surface area or diffuse pulmonary hemorrhage). Patients were randomly assigned to undergo plasma exchange (seven plasma exchanges within 14 days after randomization) or no plasma exchange (control group). Patients were also randomly assigned to follow either a standard-dose regimen or a reduced-dose regimen of oral glucocorticoids. Patients were followed for up to 7 years for the primary composite outcome of death from any cause or end-stage kidney disease (ESKD).
Death from any cause or ESKD occurred in 100 of 352 patients (28.4%) in the plasma-exchange group and in 109 of 352 patients (31.0%) in the control group (hazard ratio, 0.86; 95% confidence interval [CI], 0.65 to 1.13; P=0.27). The results were similar in subgroup analyses and in analyses of secondary outcomes. We also assessed the noninferiority of a reduced-dose regimen of glucocorticoids to a standard-dose regimen, using a noninferiority margin of 11 percentage points. Death from any cause or ESKD occurred in 92 of 330 patients (27.9%) in the reduced-dose group and in 83 of 325 patients (25.5%) in the standard-dose group (absolute risk difference, 2.3 percentage points; 90% CI, ?3.4 to 8.0), which met the criterion for noninferiority. Serious infections at 1 year were less common in the reduced-dose group than in the standard-dose group (incidence rate ratio, 0.69; 95% CI, 0.52 to 0.93), but other secondary outcomes were similar in the two groups.
Among patients with severe ANCA-associated vasculitis, the use of plasma exchange did not reduce the incidence of death or ESKD. A reduced-dose regimen of glucocorticoids was noninferior to a standard-dose regimen with respect to death or ESKD.