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Ofatumumab for B cell depletion in patients with systemic lupus erythematosus who are allergic to rituximab.

Authors :
Masoud, Sherry
McAdoo, Stephen P
Bedi, Rachna
Cairns, Thomas D
Lightstone, Liz
Source :
Rheumatology; Jul2018, Vol. 57 Issue 7, p1156-1161, 6p, 1 Chart, 1 Graph
Publication Year :
2018

Abstract

Objective. B cell depletion, most commonly with rituximab, is an evolving therapeutic approach in SLE. Infusion reactions after rituximab are common, and may prevent re-treatment in patients who previously demonstrated beneficial response. We have used ofatumumab, a fully humanized anti-CD20 mAb, as an alternative B cell-depleting agent in patients with SLE who are rituximab-intolerant due to severe infusion reactions. Methods. A single-centre retrospective case series of 16 patients were treated with ofatumumab for SLE between 2012 and 2015. Results. Ofatumumab infusion was well tolerated in 14/16 patients, in whom the median age was 34 (range 19-55) and the median duration of SLE 9.2 years (0.6-28.5). The cohort was heavily pre-treated, with 50% having prior CYC exposure, and a median cumulative dose of prior rituximab 4 g (1-6). Twelve patients were treated for LN, one for extra-renal flare and one for remission maintenance. B cell-depletion was achieved in 12/14 patients, with comparable reconstitution kinetics to a previous cohort treated with rituximab at our centre, and was associated with improvements in serological markers of disease activity, including ANA, anti-dsDNA antibody and complement levels. Half of the patients with LN achieved renal remission by 6 months. Progressive disease that was unresponsive to augmented immunosuppression with CYC was seen in five patients. During long-term follow-up (median 28 months), five grade III infections were reported, and there were no malignancies or deaths. Conclusion. In this pre-treated cohort with long-standing SLE, ofatumumab was a well-tolerated, safe and effective alternative to rituximab for B cell-depletion therapy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14620324
Volume :
57
Issue :
7
Database :
Complementary Index
Journal :
Rheumatology
Publication Type :
Academic Journal
Accession number :
130313433
Full Text :
https://doi.org/10.1093/rheumatology/key042