학술논문

Comparison of treatment options in adults with frequently relapsing or steroid-dependent minimal change disease.
Document Type
Article
Source
Nephrology Dialysis Transplantation. Oct2021, Vol. 36 Issue 10, p1821-1827. 7p.
Subject
*CALCINEURIN
*CYCLOPHOSPHAMIDE
*MYCOPHENOLIC acid
*RITUXIMAB
*DISEASE progression
Language
ISSN
0931-0509
Abstract
Background Studies comparing all treatment options for frequently-relapsing/steroid-dependent (FR/SD) minimal change disease (MCD) in adults are lacking. Methods Medical records of 76 adults with FR/SD MCD who were treated with corticosteroids as the first-line therapy were reviewed. Treatment options were compared for the time to relapse, change of therapy and progression (relapse on full-dose treatment). Results Second-line treatments included rituximab (RTX; n  = 13), mycophenolate mofetil (MMF; n  = 12), calcineurin inhibitors (CNI; n  = 26) and cyclophosphamide (CTX; n  = 16). During the second-line treatments, 48 (71.6%) patients relapsed at median 17 (range 2–100)  months. The majority of relapses occurred during dose tapering or off drug. Twenty of 65 (30.8%) changed therapy after the first relapse. The median time to relapse after the second line was 66 versus 28 months in RTX versus non-RTX groups (P = 0.170). The median time to change of treatment was 66 and 44 months, respectively (P = 0.060). Last-line treatment options included RTX (n  = 8), MMF (n  = 4), CNI (n  = 3) and CTX (n  = 2). Seven (41.2%) patients had a relapse during the last-line treatment at median 39 (range 5–112)  months. The median time to relapse was 48 versus 34 months in the RTX versus non-RTX groups (P = 0.727). One patient in the RTX group died presumably of heart failure. No major adverse event was observed. During the median follow-up of 81 (range 9–355)  months, no patients developed end-stage renal disease. Conclusions Relapse is frequent in MCD in adults. Patients treated with RTX may be less likely to require a change of therapy and more likely to come off immunosuppressive drugs. [ABSTRACT FROM AUTHOR]