Impact of belimumab therapy on the quality of life in patients with systemic lupus erythematosus: A cohort study

Author:

Prete Marcella1,Susca Nicola1,Leone Patrizia1ORCID,De Giacomo Andrea2,Bray Antonella1,Brunori Giuliano3,Favoino Elvira4,Perosa Federico4,Racanelli Vito5ORCID

Affiliation:

1. Department of Interdisciplinary Medicine, Internal Medicine Unit, “Aldo Moro” University of Bari Medical School, Bari, Italy

2. Department of Biomedical Sciences, Neuroscience, and Sense Organs, Child Neuropsychiatry Unit, “Aldo Moro” University of Bari Medical School, Bari, Italy

3. Nephrology and Dialysis, Santa Chiara Hospital, Trento, Italy

4. Department of Interdisciplinary Medicine, Rheumatological and Autoimmune Systemic Diseases Unit, “Aldo Moro” University of Bari Medical School, Bari, Italy

5. Centre for Medical Sciences, CISMed, Department of Internal Medicine, Santa Chiara Hospital, University of Trento, Trento, Italy

Abstract

Systemic lupus erythematosus (SLE) is a chronic and extremely disabling connective-tissue autoimmune disease with a tremendous impact on the quality of life (QoL). Belimumab, a B-lymphocyte-stimulator-specific inhibitor, is the first biologic drug approved as add-on therapy in patients with active, refractory auto-antibody-positive SLE. The impact of belimumab on the QoL of SLE patients was evaluated using a generic questionnaire short-form health survey 36 (SF-36) and the disease-specific questionnaire SLE-specific quality of life (SLEQoL). The Italian version of the SLEQoL and the SF-36 were administered to 46 SLE patients before and after 6 months of belimumab therapy. The control population consisted of 40 age-matched healthy individuals. The questionnaires were completed before and after belimumab treatment and the results were compared using the Wilcoxon signed-rank test. In addition, data from healthy controls and SLE patients were compared using the Mann–Whitney test. Dichotomous variables were compared using Fisher’s exact test. For SLE patients, the addition of belimumab to their therapeutic regimen significantly improved their health-related QoL (HRQoL), according to the results of the SF-36 and SLEQoL. The comparison of the data obtained before and after belimumab treatment showed a decrease in all six SLEQoL domains and an increase in all eight SF-36 domains. Moreover, treatment led to a reduction in the median prednisone dose, to 0 mg/day (IQR 0–4.5 mg/day). Before belimumab therapy, SLE patients had a worse HRQoL than the control group, based on both questionnaires, but after belimumab treatment the outcome scores between SLE patients and controls were similar, suggesting that belimumab therapy resulted in a strong improvement in HRQoL. These findings were supported by a decrease in the SELENA-SLEDAI score, a measure of disease activity. In addition to clinical remission and low disease activity, the goals of an innovative therapeutic strategy for SLE should include the attainment of a good HRQoL. Our study demonstrates that the combined use of the SF-36 and SLEQoL questionnaires can provide clinicians with a better understanding of the HRQoL of SLE patients.

Publisher

SAGE Publications

Subject

Rheumatology

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