Rituximab usage in systemic lupus erythematosus-associated antiphospholipid syndrome: A single-center experience.

Semin Arthritis Rheum

Department of Internal Medicine, Section of Rheumatology and Immunology, National Cheng Kung University Hospital, Tainan, Taiwan.

Published: August 2016

AI Article Synopsis

  • The study explores the effectiveness of rituximab in treating systemic lupus erythematosus (SLE)-associated antiphospholipid syndrome (APS) among hospitalized patients.
  • There were 63 cases of SLE-associated APS, with six patients receiving rituximab, showing no recurrence of thrombosis and a decline in lupus activity over an average follow-up of almost 40 months.
  • The findings suggest rituximab could be beneficial, prompting future research for larger trials to confirm its role in diverse patient populations.

Article Abstract

Objectives: Although the data from primary antiphospholipid syndrome (APS) suggests a beneficial effect of rituximab usage, its therapeutic role remains to be defined in systemic lupus erythematosus (SLE)-associated APS, a complex clinical situation with thrombotic events and lupus activity.

Methods: A single-center retrospective analysis of rituximab usages in APS was performed in 800 hospitalized SLE patients.

Results: There were 63 SLE-associated APS cases with 6 on rituximab therapy, all female aged 37.7 ± 9.0 years with 1 catastrophic and 16 thrombotic episodes. Therapeutic indications included warfarin failure despite the adequate target international normalized ratio with an average duration of 17.3 ± 11.2 months between the thrombotic recurrences. After the rituximab therapy, there was no relapse of thrombosis with a mean follow-up period of 39.3 ± 20.9 months, and a decrease in lupus activity (SLEDAI-2K, 9.7 ± 5.5 to 5.3 ± 2.2). Infection complications were observed, including episodes of bronchitis and urinary tract infection.

Conclusions: In this single-center study with largest case numbers and a long-term follow-up period, there were no recurrent thrombotic events after the rituximab therapy, implicating further consideration of large-scale trials enrolling more ethnic groups to evaluate its therapeutic role in SLE-associated APS patients.

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Source
http://dx.doi.org/10.1016/j.semarthrit.2016.02.002DOI Listing

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