Citation

BibTex format

@article{Masoud:2018:rheumatology/key042,
author = {Masoud, S and McAdoo, SP and Bedi, R and Cairns, T and Lightstone, L},
doi = {rheumatology/key042},
journal = {Rheumatology},
pages = {1156--1161},
title = {Ofatumumab for B cell depletion in patients with systemic lupus erythematosus who are allergic to rituximab},
url = {http://dx.doi.org/10.1093/rheumatology/key042},
volume = {57},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - ObjectiveB 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.MethodsA single-centre retrospective case series of 16 patients were treated with ofatumumab for SLE between 2012 and 2015.ResultsOfatumumab 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.ConclusionIn this pre-treated cohort with long-standing SLE, ofatumumab was a well-tolerated, safe and effective alternative to rituximab for B cell–depletion therapy.
AU - Masoud,S
AU - McAdoo,SP
AU - Bedi,R
AU - Cairns,T
AU - Lightstone,L
DO - rheumatology/key042
EP - 1161
PY - 2018///
SN - 1462-0324
SP - 1156
TI - Ofatumumab for B cell depletion in patients with systemic lupus erythematosus who are allergic to rituximab
T2 - Rheumatology
UR - http://dx.doi.org/10.1093/rheumatology/key042
VL - 57
ER -