BURDEN OF DISEASE IN SYSTEMIC LUPUS ERYTHEMATOSUS PATIENTS TREATED WITH CORTICOSTEROIDS

Author(s)

Strand V1, Johnson J2, Vandeloo C3, Galateanu C3, Lobosco S2
1Biopharmaceutical Consultant, Portola Valley, CA, USA, 2Adelphi Real World Ltd, Macclesfield, UK, 3UCB Pharma, Brussels, Belgium

OBJECTIVES: Current treatments for systemic lupus erythematosus (SLE) include corticosteroids (CS), immunosuppressants (IM), antimalarials (AM) and biologics. SLE treatments, in particular CS, are associated with adverse effects which impact tolerability and treatment-burden. This study sought to assess the use of CS in SLE, and the burden associated with this treatment class. METHODS: Data were extracted from the Adelphi 2013 Lupus Disease-Specific Programme (a multinational survey of clinical practice). Physicians completed Patient Record Forms (PRFs) and underwent face-to-face interviews; patients self-reported data including the EQ-5D, Work Productivity & Activity Impairment Index for SLE (WPAI-Lupus) and Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) in Patient Self-Completion Records (PSCs). Patient eligibility was determined by physicians; disease activity and severity were based on physician and patient assessment. RESULTS: Data were collected from rheumatologists in the US (n=97), France (n=37) and Germany (n=35), including PRFs (550/200/207, respectively) and PSCs (303/109/149, respectively). 57%/84%/89% of patients in the US/France/Germany were receiving CS treatment. CS were perceived to be equal/superior to AM, IM and biologics in the ability to rapidly treat flare and pain but inferior in terms of safety/tolerability and inhibition of disease progression. More than half of patients had concerns regarding CS treatment, mainly due to side-effects and fear of long-term use. Patients receiving CS had greater resource use (increased IM/biologic use, greater physician consultation and hospitalisation) and worse HRQoL and activity impairment vs non-CS patients (EQ-5D=0.78 vs 0.87; FACIT-F=34.41 vs 39.56; WPAI=23.30 vs 13.22), but were also associated with worse clinical status (more ‘moderate severe’ SLE, more ‘deteriorating’ disease state, more rash/pain/flaring/depression, greater organ system involvement). CONCLUSIONS: Although a major component of SLE standard of care, clear unmet needs are associated with CS use regarding HRQoL and resource use.  Long-term safety and tolerability are also major areas of concern for both physicians and patients.

Conference/Value in Health Info

2014-05, ISPOR 2014, Palais des Congres de Montreal

Value in Health, Vol. 17, No. 3 (May 2014)

Code

PSY54

Topic

Patient-Centered Research

Topic Subcategory

Stated Preference & Patient Satisfaction

Disease

Systemic Disorders/Conditions

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