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
. 2021 Nov;8(1):e000538.
doi: 10.1136/lupus-2021-000538.

2021 DORIS definition of remission in SLE: final recommendations from an international task force

Affiliations

2021 DORIS definition of remission in SLE: final recommendations from an international task force

Ronald F van Vollenhoven et al. Lupus Sci Med. 2021 Nov.

Erratum in

Abstract

Objective: To achieve consensus on a definition of remission in SLE (DORIS).

Background: Remission is the stated goal for both patient and caregiver, but consensus on a definition of remission has been lacking. Previously, an international task force consisting of patient representatives and medical specialists published a framework for such a definition, without reaching a final recommendation.

Methods: Several systematic literature reviews were performed and specific research questions examined in suitably chosen data sets. The findings were discussed, reformulated as recommendations and voted on.

Results: Based on data from the literature and several SLE-specific data sets, a set of recommendations was endorsed. Ultimately, the DORIS Task Force recommended a single definition of remission in SLE, based on clinical systemic lupus erythematosus disease activitiy index (SLEDAI)=0, Evaluator's Global Assessment <0.5 (0-3), prednisolone 5 mg/day or less, and stable antimalarials, immunosuppressives, and biologics.

Conclusion: The 2021 DORIS definition of remission in SLE is recommended for use in clinical care, education, and research including clinical trials and observational studies.

Keywords: healthcare; lupus erythematosus; outcome assessment; systemic; therapeutics.

PubMed Disclaimer

Conflict of interest statement

Competing interests: RFvV has received research and educational support (grants) from BMS, GSK, Lilly, Pfizer, Roche and UCB; and reimbursement for consultancy and/or speaking from AbbVie, AstraZeneca, Biogen, Biotest, BMS, Galapagos, Gilead, GSK, Janssen, Pfizer, Sanofi, Servier, UCB and Vielabio. RC—GSK, Alexion, Eli Lilly, AstraZeneca, Termo-Fisher and Rubió. BAP-E—GSK and Janssen. MFU-G received research grants from Janssen and Pfizer. LA acted as a consultant for Alexion, Amgen, AstraZeneca, BMS, GSK, Janssen-Cilag, LFB, Lilly, Menarini France, Medac, Novartis, Pfizer, Roche-Chugaï and UCB. CG—personal fees for honoraria from consultancy work from the Center for Disease Control, AstraZeneca, MGP, Sanofi and UCB; and personal fees for speaker’s bureau from UCB. HBo—unrestricted grants from Bristol-Myers Squibb and Roche; consultant for Bristol-Myers Squibb, Roche, Novartis, Medimmune and Union Chimique Belge; speaker for Bristol-Myers Squibb and Novartis; member of the advisory board of Bristol-Myers Squibb, Novartis and Sanofi. MI—consultations from GSK and Amgen. DJ—AstraZeneca, Aurinia, BMS, Boehringer-Ingelheim, Chemocentryx, Chugai, CSL, GSK, Infla-RX, Janssen, Novartis, Roche/Genentech, Takeda and Vifor. AK—honoraria from Bristol-Myers Squibb, KGaA, GlaxoSmithKline, Janssen Cilag and Lilly Deutschland. ML—receipts from GSK for advisory boards and sponsoring of investigator-initiated study. MN—research support from Actelion, AstraZeneca, BMS, GSK, Janssen and UCB; and honoraria from Actelion, Boehringer Ingelheim, Eli Lilly, GSK, Janssen, Pfizer and UCB. AT—consultation/speaker fees from UCB, GSK, Novartis and Janssen.

References

    1. van Vollenhoven R. Treat-to-target in rheumatoid arthritis - are we there yet? Nat Rev Rheumatol 2019;15:180–6. 10.1038/s41584-019-0170-5 - DOI - PubMed
    1. Zhang AD, Kavanaugh A. Treat to target in psoriatic arthritis. Rheum Dis Clin North Am 2019;45:505–17. 10.1016/j.rdc.2019.07.002 - DOI - PubMed
    1. van Vollenhoven RF, Mosca M, Bertsias G, et al. . Treat-to-target in systemic lupus erythematosus: recommendations from an international Task force. Ann Rheum Dis 2014;73:958–67. 10.1136/annrheumdis-2013-205139 - DOI - PubMed
    1. van Vollenhoven R, Voskuyl A, Bertsias G, et al. . A framework for remission in SLE: consensus findings from a large international Task force on definitions of remission in SLE (DORIS). Ann Rheum Dis 2017;76:554–61. 10.1136/annrheumdis-2016-209519 - DOI - PubMed
    1. Ugarte-Gil MF, Mendoza Pinto C, Pons-Estel G. AB0448 IMPACT OF REMISSION ON DAMAGE ACCRUAL IN SYSTEMIC LUPUS ERYTHEMATOSUS (SLE) PATIENTS: A SYSTEMATIC LITERATURE REVIEW (SLR). Ann Rheum Dis 2020;79:1518–22. 10.1136/annrheumdis-2020-eular.2037 - DOI

Publication types

MeSH terms