About this trial
Lupus Low Disease Activity State (LLDAS) study is an international, multi-centre prospective study, developed by the Asia Pacific Lupus Collaboration (APLC) to investigate whether the attainment of LLDAS is associated with improved outcomes in patients with Systemic Lupus Erythematosus (SLE).
SLE, or lupus, is the archetypal multisystem autoimmune disease, with an estimated incidence of 5-50 cases per 100,000 people. Patients with SLE, usually young women, suffer a marked loss of life expectancy, and severe morbidity, due to a heterogeneous range of clinical manifestations caused by autoimmune-mediated inflammation of multiple organs. The most severe manifestations of SLE are the accrual of irreversible organ damage, especially renal and central nervous system (CNS) involvement. As there is no effective targeted monotherapy for SLE, patients also suffer severe toxicity from the use of glucocorticoids and broad-spectrum immunosuppressive therapies. Despite combination therapy with current drugs, many studies show that the majority of patients suffer inadequate disease control and inexorably accrue permanent organ damage over time.
The diversity of clinical features of active SLE has made quantification of disease activity problematic. Although there are a number of published systems in use to measure SLE disease activity, there are widely acknowledged problems with these instruments. Published definitions of remission are so stringent that they are met by less than 5% of patients. This lead to the realisation that rather than lupus remission, a lupus low disease activity state target may be more feasible, and that patients with low disease activity are more homogeneous than patients with active disease. Thus, the development of a definition of lupus low disease activity, which is feasible and has face validity, escapes the complexity of attempts to quantify heterogeneous states of active disease.
In this study, the investigators will prospectively collect longitudinal data on consecutive SLE patients at each centre to evaluate the LLDAS definition. Protection from organ damage accrual as the primary endpoint.
Eligibility criteria
Qualifiers
All patients have to meet either the 1997 American College of Rheumatology (ACR) Modified Classification Criteria for SLE, with at least four of the 11 items; or alternatively, fulfil the Systemic Lupus International Collaborating Clinics (SLICC) 2012 Classification Criteria, with at least four of the 17 items (at least one clinical and one immunological criterion) or with lupus nephritis in the presence of at least one immunological criteria. Patients can be either newly diagnosed or longstanding lupus patients.
Disqualifiers
Patients less than 18 years of age and patients who are unable to consent are excluded from the study.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Monash University
Lead sponsor
Flinders Medical Centre, Adelaide, AUSTRALIA
Collaborator
St. Vincent's Hospital, Melbourne, AUSTRALIA
Collaborator
Royal Adelaide Hospital
Collaborator
The University of New South Wales
Collaborator
People's Hospital, Peking University Health Science Center, Beijing, CHINA
Collaborator
Peking University First Hospital
Collaborator
The University of Hong Kong
Collaborator
University of Padjadjaran, Bandung, INDONESIA
Collaborator
Tokyo Women's Medical University, JAPAN
Collaborator
University of Occupational and Environmental Health, JAPAN
Collaborator
Keio University, JAPAN
Collaborator
Hanyang University Seoul Hospital
Collaborator
University of Santo Tomas Hospital, Philippines
Collaborator
National University Hospital, Singapore
Collaborator
Tan Tock Seng Hospital
Collaborator
Chang Gung Memorial Hospital
Collaborator
Taichung Veterans General Hospital
Collaborator
Chiang Mai University Hospital, THAILAND
Collaborator
Middlemore Hospital, New Zealand
Collaborator
North Shore Hospital, Auckland, NEW ZEALAND
Collaborator
Auckland District Health Board
Collaborator
Teaching Hospital Kandy, SRI LANKA
Collaborator
University of the Philippines
Collaborator