Original Article

Outcomes of rituximab therapy in refractory lupus: A meta-analysis

Volume 5 · Issue 2 Publish Date: September 3, 2019
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Fatma Alshaiki
Department of Medicine, East Jeddah Hospital, Jeddah, Saudi Arabia
Elaf Obaid
Department of Medicine, Umm Al-Qura University School of Medicine, Makkah, Saudi Arabia
Abdulqader Almuallim
Department of Medicine, Umm Al-Qura University School of Medicine, Makkah, Saudi Arabia
Rabab Taha
Department of Medicine, Dr. Sloiman Fakeeh Hospital, Jeddah, Saudi Arabia
Hadeel El-haddad
Department of Medicine, Dr. Sloiman Fakeeh Hospital, Jeddah, Saudi Arabia
Hani Almoallim
Department of Medicine, Umm Al-Qura University School of Medicine, Makkah; Department of Medicine, Dr. Sloiman Fakeeh Hospital, Jeddah; Alzaidi Chair of Research in Rheumatic Diseases, Umm Al-Qura University, Makkah, Saudi Arabia
Alshaiki, F., Obaid, E., Almuallim, A., Taha, R., El-haddad, H., & Almoallim, H. (2019). Outcomes of rituximab therapy in refractory lupus: A meta-analysis. European Journal of Rheumatology, 5(2), 118–126. https://doi.org/10.5152/eurjrheum.2018.17096
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Abstract

Abstract

 

Objective: Conventional treatment of systemic lupus erythematosus (SLE) and lupus nephritis (LN) is associated with damage accrual, hence increased morbidity rate. Off-label use of rituximab (RTX) has shown significant promise in this patient group; however, data are still controversial. We aimed to analyze the outcomes of RTX therapy in refractory lupus using a meta-analysis approach.

 

Methods: Electronic search of the medical literature was conducted using a combination of relevant keywords to retrieve studies on the safety and efficacy of RTX in SLE and LN patients. Results were screened against our inclusion and exclusion criteria and two reviewers independently extracted the data for analysis. Comprehensive meta-analysis software was used to pool the data from individual studies and provide summary effect estimates.

 

Results: Thirty-one studies that enrolled 1112 patients were finally eligible for the meta-analysis. The overall global, complete, and partial response rates to RTX therapy were 72%, 46%, and 32%, respectively. RTX significantly decreased Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and British Isles Lupus Activity Group (BILAG) scores (p<0.001). Prednisone dose was significantly reduced after RTX treatment in both SLE and LN groups (p<0.001), and proteinuria was lowered in SLE (p<0.001) than in LN patients (p=0.07). Infection and infusion-related reactions were the most common side effects.

 

Conclusion: RTX therapy in refractory SLE and LN patients proved clinical efficacy and favorable safety outcomes. Larger well-designed randomized clinical trials are warranted.

 

Cite this article as: Alshaiki F, Obaid E, Almuallim A, Taha R, El-haddad H, Almoallim H. Outcomes of rituximab therapy in refractory lupus: A meta-analysis. Eur J Rheumatol 2018; 5: 118-26.

Article Info
Published In
Journal European Journal of Rheumatology
Volume / Issue Volume 5 · Issue 2
Pages 118-126
History
Published Online September 3, 2019
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Affiliations
Fatma Alshaiki
Department of Medicine, East Jeddah Hospital, Jeddah, Saudi Arabia
Elaf Obaid
Department of Medicine, Umm Al-Qura University School of Medicine, Makkah, Saudi Arabia
Abdulqader Almuallim
Department of Medicine, Umm Al-Qura University School of Medicine, Makkah, Saudi Arabia
Rabab Taha
Department of Medicine, Dr. Sloiman Fakeeh Hospital, Jeddah, Saudi Arabia
Hadeel El-haddad
Department of Medicine, Dr. Sloiman Fakeeh Hospital, Jeddah, Saudi Arabia
Hani Almoallim
Department of Medicine, Umm Al-Qura University School of Medicine, Makkah; Department of Medicine, Dr. Sloiman Fakeeh Hospital, Jeddah; Alzaidi Chair of Research in Rheumatic Diseases, Umm Al-Qura University, Makkah, Saudi Arabia
Cite this Article
Alshaiki, F., Obaid, E., Almuallim, A., Taha, R., El-haddad, H., & Almoallim, H. (2019). Outcomes of rituximab therapy in refractory lupus: A meta-analysis. European Journal of Rheumatology, 5(2), 118–126. https://doi.org/10.5152/eurjrheum.2018.17096
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