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Rituximab therapy in patients with bullous pemphigoid: A retrospective study of 20 patients
Bullous pemphigoid (BP) is the most common autoimmune blistering disease requiring treatment with immunosuppressive medications; however, finding a therapy that has a sustained durable response and an acceptable side effect profile has been challenging. Our study aimed to evaluate the clinical outco...
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Published in: | Journal of the American Academy of Dermatology 2019-07, Vol.81 (1), p.179-186 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Bullous pemphigoid (BP) is the most common autoimmune blistering disease requiring treatment with immunosuppressive medications; however, finding a therapy that has a sustained durable response and an acceptable side effect profile has been challenging.
Our study aimed to evaluate the clinical outcomes of patients with BP treated with rituximab therapy at a single academic center.
A retrospective chart review was performed on 20 patients who received at least 1 dose of rituximab therapy, either as initial therapy for severe BP or as therapy for recalcitrant disease after having failed conventional immunotherapies.
Within our cohort, 75% of patients (n = 15) achieved remission an average of 169 days following rituximab therapy. There were no rituximab-related deaths and significantly fewer adverse events following rituximab therapy.
This study was limited by its retrospective nature, focus on a single academic center, and small sample size.
Use of rituximab therapy demonstrated high rates of remission, steroid-sparing activity, and an acceptable safety profile in our cohort of patients with severe BP or disease refractory to conventional therapies. |
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ISSN: | 0190-9622 1097-6787 |
DOI: | 10.1016/j.jaad.2019.03.049 |