TY - JOUR
T1 - Targeting DORIS Remission and LLDAS in SLE
T2 - A Review
AU - Parra Sánchez, Agner R.
AU - van Vollenhoven, Ronald F.
AU - Morand, Eric F.
AU - Bruce, Ian N.
AU - Kandane-Rathnayake, Rangi
AU - Weiss, Gudrun
AU - Tummala, Raj
AU - Al-Mossawi, Hussein
AU - Sorrentino, Alessandro
N1 - Funding Information: Medical writing support and editorial assistance was provided by Tamsin Brown, MSc, of JK Associates Inc., part of Fishawack Health. This support was funded by AstraZeneca. Funding Information: Agner R. Parra Sánchez has received grant/research support (institutional grants) from AstraZeneca; received support for attending meetings and/or travel from Amsterdam UMC. The work of ARPS is supported by the European Union’s Horizon 2020 research and innovation program (“ARCAID”; www.arcaid-h2020.eu ; grant agreement nr. 847551). Ronald F. van Vollenhoven has received grant/research support from Bristol Myers Squibb (BMS) and UCB; received support for educational programs from AstraZeneca, Galapagos, MSD, Novartis, Pfizer, Roche, Sanofi, and UCB; received consulting fees from AbbVie, AstraZeneca, Biogen, BMS, Galapagos, Janssen, Pfizer, and UCB; and received speaking fees and/or honoraria from AbbVie, AstraZeneca, BMS, Galapagos, GlaxoSmithKline (GSK), Janssen, Pfizer, and UCB. Eric F. Morand has received grant support from AbbVie, Amgen, AstraZeneca, Biogen, BMS, Eli Lilly and Company, EMD Serono, Genentech, GSK, Janssen, and UCB Pharma; received consulting fees from AbbVie, Amgen, AstraZeneca, Biogen, BMS, Eli Lilly and Company, EMD Serono, Genentech, GSK, Janssen, Novartis, Servier, Wolf, and Zenas; received speaking fees and/or honoraria from AstraZeneca, Biogen, BMS, EMD Serono, and Gilead; received support for attending meetings and/or travel from AstraZeneca; and served in a leadership or fiduciary role as Board Director at Rare Voices Australia. Ian N. Bruce is a National Institute for Health Research (NIHR) Senior Investigator and is funded by the NIHR Manchester Biomedical Research Centre (NIHR 203308). His institution has received research grants from GSK and Genzyme/Sanofi and consultancy fees from GSK, UCB, Eli Lilly, BMS, Merck Serono, Aurinia and IL-TOO. Dr Bruce has received speaker fees from GSK, AstraZeneca and UCB; he also participated on a Data Safety Monitoring Board or Advisory Board for AstraZeneca and Merck Serono. Rangi Kandane-Rathnayake declares that there is no conflict of interest. Gudrun Weiss, Raj Tummala, and Hussein Al-Mossawi are all employees of and may hold stock in AstraZeneca. Alessandro Sorrentino is an employee of AstraZeneca and holds stock in Abbott, Galapagos, Gilead, and Moderna. Funding Information: Medical writing support and editorial assistance was provided by Tamsin Brown, MSc, of JK Associates Inc., part of Fishawack Health. This support was funded by AstraZeneca. Publisher Copyright: © 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Remission is the established therapeutic goal for patients with systemic lupus erythematosus (SLE) and is currently defined by the widely adopted Definition Of Remission In SLE (DORIS) criteria. Attainment of remission is rare in the clinical setting, thus an alternative, pragmatic treatment target of low disease activity, as defined by the Lupus Low Disease Activity State (LLDAS), provides a less stringent and more attainable treatment goal for a wider proportion of patients compared with DORIS remission. Randomized controlled trials and real-world analyses have confirmed the positive clinical benefits of achieving either DORIS remission or LLDAS. The treat-to-target (T2T) approach utilizes practical clinical targets to proactively tailor individual treatment regimens. Studies in other chronic inflammatory diseases using the T2T approach demonstrated significantly improved clinical outcomes and quality-of-life measures compared with established standard of care. However, such trials have not yet been performed in patients with SLE. Here we review the evolution of DORIS remission and LLDAS definitions and the evidence supporting the positive clinical outcomes following DORIS remission or LLDAS attainment, before discussing considerations for implementation of these outcome measures as potential T2T objectives. Adoption of DORIS remission and LLDAS treatment goals may result in favorable patient outcomes compared with established standard of care for patients with SLE.
AB - Remission is the established therapeutic goal for patients with systemic lupus erythematosus (SLE) and is currently defined by the widely adopted Definition Of Remission In SLE (DORIS) criteria. Attainment of remission is rare in the clinical setting, thus an alternative, pragmatic treatment target of low disease activity, as defined by the Lupus Low Disease Activity State (LLDAS), provides a less stringent and more attainable treatment goal for a wider proportion of patients compared with DORIS remission. Randomized controlled trials and real-world analyses have confirmed the positive clinical benefits of achieving either DORIS remission or LLDAS. The treat-to-target (T2T) approach utilizes practical clinical targets to proactively tailor individual treatment regimens. Studies in other chronic inflammatory diseases using the T2T approach demonstrated significantly improved clinical outcomes and quality-of-life measures compared with established standard of care. However, such trials have not yet been performed in patients with SLE. Here we review the evolution of DORIS remission and LLDAS definitions and the evidence supporting the positive clinical outcomes following DORIS remission or LLDAS attainment, before discussing considerations for implementation of these outcome measures as potential T2T objectives. Adoption of DORIS remission and LLDAS treatment goals may result in favorable patient outcomes compared with established standard of care for patients with SLE.
KW - DORIS remission
KW - LLDAS
KW - Low disease activity
KW - Remission
KW - Systemic lupus erythematosus
KW - Treat-to-target approach
UR - http://www.scopus.com/inward/record.url?scp=85173726892&partnerID=8YFLogxK
U2 - https://doi.org/10.1007/s40744-023-00601-w
DO - https://doi.org/10.1007/s40744-023-00601-w
M3 - Review article
C2 - 37798595
SN - 2198-6576
VL - 10
SP - 1459
EP - 1477
JO - Rheumatology and therapy
JF - Rheumatology and therapy
IS - 6
ER -