The effects of golimumab on patient centric outcomes amongst rheumatoid arthritis patients in Greece. The GO-Q study.

Dimitrios Psaltis, Loukas Settas, Athanasios Georgiadis, Eftichia Koukli, Andreas Bounas, Achilleas Livieratos, Evangelia Petrikkou, Heleni Kalogiannaki, Argyro Repa, Dimitrios Vassilopoulos, Prodromos Sidiropoulos
Author Information
  1. Dimitrios Psaltis: Private Practice, Serres, Greece. ORCID
  2. Loukas Settas: University of Thessaloniki, Thessaloniki, Greece.
  3. Athanasios Georgiadis: Private Practice, Ioannina, Greece. ORCID
  4. Eftichia Koukli: Private Practice, Athens, Greece.
  5. Andreas Bounas: OLYMPION"-General Clinic of Patra, Patras, Greece.
  6. Achilleas Livieratos: MSD Pharmaceutical, Industrial and Commercial S.A., Medical Affairs, Athens, Greece. ORCID
  7. Evangelia Petrikkou: MSD Pharmaceutical, Industrial and Commercial S.A., Medical Affairs, Athens, Greece.
  8. Heleni Kalogiannaki: Department of Rheumatology, Clinical Immunology and Allergy, University of Crete Medical School, Heraklion, Greece.
  9. Argyro Repa: Department of Rheumatology, Clinical Immunology and Allergy, University of Crete Medical School, Heraklion, Greece. ORCID
  10. Dimitrios Vassilopoulos: 2nd Department of Medicine and Laboratory Clinical Immunology-Rheumatology Unit, Hippokration General Hospital, National and Kapodistrian University of Athens School of Medicine, Athens, Greece. ORCID
  11. Prodromos Sidiropoulos: Department of Rheumatology, Clinical Immunology and Allergy, University of Crete Medical School, Heraklion, Greece. sidiropp@uoc.gr. ORCID

Abstract

This study aimed at assessing the impact of golimumab on health-related quality of life (HRQoL) and other patient-reported outcomes (PROs) in patients with rheumatoid arthritis (RA) in real-world settings. GO-Q was an observational, prospective, 12-month study, which recruited patients with moderate-to-severely active RA initiating golimumab treatment per label in rheumatology clinics and private practices. Primary endpoint was the change in PROs [EuroQol-5 Dimensions-3 Levels (EQ-5D-3L) questionnaire, Health Assessment Questionnaire Disease Index (HAQ-DI), and Work Productivity and Activity Index for RA (WPAI:RA)] after 12 months of treatment. Other endpoints included Disease Activity Score for 28 joints with erythrocyte sedimentation rate (DAS28-ESR), healthcare resource utilization, and golimumab adherence. Changes in continuous variables from baseline were evaluated with the paired t test. One hundred forty-five patients were recruited. The mean [standard deviation (SD)] EQ-5D-3L index increased significantly at 12 months versus baseline [from 0.427 (0.206) to 0.801 (0.229); p < 0.0001], with changes as early as 3 and 6 months (both p < 0.0001). Accordingly, there were statistically significant changes in all WPAI:RA domains from baseline to 3, 6, and 12 months (p < 0.0001). Patients' function improved gradually from the third month until the end of follow-up (p < 0.0001 for all time-points). Thirty (27.3%) and 60 (54.6%) patients achieved remission (DAS28-ESR < 2.6) and low disease activity (DAS28-ESR ≤ 3.2), respectively, at 12 months. Adherence rate to golimumab was high (mean [SD] 90.3% (7.5) at 12 months). In patients with moderate-to-severely active RA, golimumab significantly improved HRQoL, physical function, and work productivity and activity, with improvements in disease activity over 12 months in real-world settings.

Keywords

References

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MeSH Term

Antibodies, Monoclonal
Antirheumatic Agents
Arthritis, Rheumatoid
Greece
Humans
Patient-Centered Care
Prospective Studies
Quality of Life
Severity of Illness Index
Treatment Outcome

Chemicals

Antibodies, Monoclonal
Antirheumatic Agents
golimumab

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