GOLIMUMAB IMPROVES QUALITY OF LIFE AND OTHER PATIENT-REPORTED OUTCOMES IN PATIENTS WITH RHEUMATOID ARTHRITIS, IN REAL-WORLD CONDITIONS

Author(s)

Psaltis D1, Settas L2, Georgiadis A3, Koukli E4, Bounas A5, Haratsis I6, Petrikkou E6, Kalogiannaki E7, Sidiropoulos P7, Vassilopoulos D8
1Private Practice, Serres, Greece, 2Private practice, Thessaloniki, Greece, 3Private Practice, Ioannina, Greece, 4Private Practice, Athens, Greece, 5Private Practice, Patras, Greece, 6Medical Affairs, Merck Sharp & Dohme Pharmaceutical, Industrial and Commercial SA, Alimos, Greece, 7Department of Rheumatology, Clinical Immunology and Allergy, University of Crete, Heraklion, Crete, Greece, 82nd Department of Internal Medicine and Laboratory, Hippokration General Hospital, Athens, Greece

Presentation Documents

OBJECTIVES

:
To assess the impact of golimumab on quality-of-life (QoL) and other patient-reported outcomes in patients with rheumatoid arthritis (RA) in real-world settings.

METHODS

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GO-Q was an observational, prospective, 12-month study conducted in Greece, in naïve to golimumab patients with moderate-to-severe active RA; patients previously treated with >1 biologic (b)DMARDs or switching anti-TNFs were excluded. Primary endpoint: the impact of golimumab on QoL at 3/6/12 months, by the EQ-5Q-3L questionnaire. Other endpoints assessed the impact of golimumab on disease activity (Disease Activity Score for 28 joints with erythrocyte sedimentation rate [DAS28-ESR]), physical function (Health Assessment Questionnaire–Disability Index [HAQ-DI]), and work productivity/activity impairment (by Work Productivity and Activity Impairment questionnaire [WPAI] for RA), at 3/6/12 months respectively. Non-parametric tests were used for all comparisons.

RESULTS

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A total of 145 patients were enrolled (age and disease duration [mean±sd]: 54.6±12.2 and 4.6±5.1 years, respectively). At baseline, 78.6% of patients were bDMARD-naïve, 87.6% had received conventional synthetic (cs)DMARDs and 77.2% corticosteroids. During follow-up, golimumab was mostly (99.4%) administered in the 50mg once-monthly dose, plus background csDMARDs. Improvements in EQ-5D-3L UK index scores from baseline to 3/6/12 months were: 0.21±0.24, 0.28±0.25, 0.38±0.30, respectively (p<0.001, all comparisons). DAS28-ESR scores improved from baseline to 3/6/12 months; mean±sd scores were 5.4±0.9, 4.1±1.2, 3.7±1.2 and 3.2±1.1, respectively (p<0.001, all comparisons). Of patients attending the 12-month visit, 27.3% and 54.6% achieved DAS28-ESR<2.6 (remission) and DAS28-ESR≤3.2 (low disease activity). Improvements were observed in HAQ-DI and WPAI scores from baseline to 3/6/12 months (p<0.001, all comparisons). Mean adherence rate to golimumab was 90.3%; non-significant difference in adherence rates for bDMARD-naïve vs. -experienced (p=0.152). Healthcare resources for RA-related reasons were utilised by >93.2% of pts.

CONCLUSIONS

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In real-world settings, patients with RA receiving golimumab over 12 months experienced significant improvements in QoL, physical function and work productivity/activity impairment.

Conference/Value in Health Info

2019-11, ISPOR Europe 2019, Copenhagen, Denmark

Code

PBI83

Topic

Economic Evaluation, Patient-Centered Research

Topic Subcategory

Patient-reported Outcomes & Quality of Life Outcomes, Work & Home Productivity - Indirect Costs

Disease

Systemic Disorders/Conditions

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