All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a healthcare professional.
The Lupus Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the Lupus Hub cannot guarantee the accuracy of translated content. The Lupus Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The Lupus Hub is an independent medical education platform, supported through sponsorship from Autolus and Biogen. Funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.
Now you can support HCPs in making informed decisions for their patients
Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.
Find out more
Create an account to access:
Bookmark & personalize site content
Receive alerts for new content in your areas of interest
View lupus content recommended for you
Results from a retrospective, multicenter, propensity-matched cohort study comparing early belimumab plus standard of care (SoC) vs SoC alone in 182 adults with lupus nephritis (LN) were published in Rheumatology by Gatto et al. Patients (N = 182; n = 91 in each arm) were matched on baseline proteinuria, estimated glomerular filtration rate, histological class, and initial immunosuppression. The primary endpoint was complete renal response (CRR).
Key data: At 6 months, the CRR rate was significantly higher with belimumab + SoC vs SoC alone (35.9% vs 16.5%; odds ratio [OR], 2.81; 95% confidence interval [CI], 1.30–6.29; p = 0.005), with a shorter median time to CRR (5.64 vs 7.92 months; p < 0.01). At the time of CRR, glucocorticoid (GC) dose was significantly lower with belimumab + SoC vs SoC alone (5 vs 15 mg/day; p = 0.018). Independent predictors of earlier CRR were belimumab use (hazard ratio [HR], 1.70; 95% CI, 1.11–2.62; p = 0.016) and baseline proteinuria (HR, 0.89; 95% CI, 0.80–0.98; p = 0.019).
Key learning: Early belimumab integration into SoC accelerates CRR and reduces GC exposure in patients with LN. These real-world findings support upfront combination therapy, particularly in patients with high disease activity.
References
Please indicate your level of agreement with the following statements:
The content was clear and easy to understand
The content addressed the learning objectives
The content was relevant to my practice
I will change my clinical practice as a result of this content