Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Aug 20;2(1):e000105.
doi: 10.1136/lupus-2015-000105. eCollection 2015.

Characteristics of azathioprine use and cessation in a longitudinal lupus cohort

Affiliations

Characteristics of azathioprine use and cessation in a longitudinal lupus cohort

Lucy Croyle et al. Lupus Sci Med. .

Abstract

Objective: Guidelines for azathioprine (AZA) use in systemic lupus erythematosus (SLE), including indications for initiation and cessation, are lacking. Clinical decision-making could be improved if reasons for cessation of AZA treatment were standardised.

Methods: We determined the characteristics of AZA use in a cohort of patients with SLE and evaluated reasons for AZA cessation. Patients with SLE in a single centre had longitudinal recording of disease activity (Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI)-2k), laboratory investigations and treatment from 2007 to 2012.

Results: Of 183 patients studied, 67 used AZA on at least one occasion. There was no significant difference between AZA users and non-users in age or American College of Rheumatology criteria. Compared with those not treated with AZA, patients treated with AZA had higher disease activity (time-adjusted mean SLEDAI 5.2±0.3 vs 3.8±0.3, p=0.0028) and damage (Systemic Lupus International Collaborating Clinics (SLICC)-SDI 1.6±0.3 vs 1.2±0.1, p=0.0445), and were more likely to have a positive dsDNA (p=0.0130) and receive glucocorticoids (p<0.0001). AZA therapy was ceased in 30/67 (45%) patients. The predominant reasons for cessation were treatment de-escalation 14 (47%), treatment failure 12 (40%) and toxicity 3 (10%). AZA was switched to mycophenolate mofetil (MMF) in 9/12 (75%) of treatment failures, and this choice was strongly associated with active lupus nephritis.

Conclusions: AZA toxicity was uncommon, and many patients ceased therapy in the context of treatment de-escalation. However, the frequent development of active lupus nephritis requiring MMF suggests the need to distinguish refractoriness, under-treatment and non-adherence to AZA in patients with SLE. These findings suggest that future studies of AZA metabolite measurement could prove valuable in the management of SLE.

Keywords: DMARDs (synthetic); Disease Activity; Systemic Lupus Erythematosus; Treatment.

PubMed Disclaimer

References

    1. Okon LG, Werth VP. Cutaneous lupus erythematosus: diagnosis and treatment. Best Pract Res Clin Rheumatol 2013;27:391–404. doi:10.1016/j.berh.2013.07.008 - DOI - PMC - PubMed
    1. Janssens P, Arnaud L, Galicier L et al. . Lupus enteritis: from clinical findings to therapeutic management. Orphanet J Rare Dis 2013;8:67 doi:10.1186/1750-1172-8-67 - DOI - PMC - PubMed
    1. American College of Rheumatology guidelines for screening, treatment, and management of lupus nephritis. 2012:797–808. - PMC - PubMed
    1. Bertsias G, Ioannidis JPA, Boletis J et al. . EULAR recommendations for the management of systemic lupus erythematosus. Report of a Task Force of the EULAR Standing Committee for International Clinical Studies Including Therapeutics; 2008:195–205. - PubMed
    1. Pego-Reigosa JM, Cobo-Ibáñez T, Calvo-Alén J et al. . Efficacy and safety of nonbiologic immunosuppressants in the treatment of nonrenal systemic lupus erythematosus: a systematic review. Arthritis Care Res 2013;65:1775–85. doi:10.1002/acr.22035 - DOI - PubMed

LinkOut - more resources