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Comparative effectiveness of TNF inhibitors and tocilizumab with and without conventional synthetic disease-modifying antirheumatic drugs in a pan-European observational cohort of bio-naïve patients with rheumatoid arthritis
K. Lauper, D. Mongin, F. Iannone, EK. Kristianslund, TK. Kvien, DC. Nordström, K. Pavelka, M. Pombo-Suarez, Z. Rotar, MJ. Santos, C. Codreanu, G. Lukina, SL. Gale, M. John, Y. Luder, DS. Courvoisier, C. Gabay
Jazyk angličtina Země Spojené státy americké
Typ dokumentu srovnávací studie, časopisecké články, pozorovací studie, práce podpořená grantem
- MeSH
- antirevmatika terapeutické užití MeSH
- dospělí MeSH
- humanizované monoklonální protilátky terapeutické užití MeSH
- inhibitory TNF terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- registrace MeSH
- revmatoidní artritida farmakoterapie MeSH
- senioři MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Geografické názvy
- Evropa MeSH
OBJECTIVES: To compare treatment effectiveness in rheumatoid arthritis (RA) patients naïve to biological disease-modifying antirheumatic drugs (bDMARDs) treated with tocilizumab (TCZ) or TNF-inhibitor (TNFi) with (-combo) or without (-mono) conventional synthetic DMARDs (csDMARDs). METHODS: Patients with RA across 7 European registries, naïve to bDMARDs who initiated treatment with TCZ or TNFi from 2009 to 2016 were included. Drug retention rate was analyzed using Kaplan-Meier and Cox models, and CDAI over time by mixed models. The proportions of patients reaching CDAI low disease activity (LDA) and remission after one year were corrected for attrition. RESULTS: 6713 TNFi-combo, 3762 TNFi-mono, 646 TCZ-combo and 384 TCZ-mono were eligible. Crude median retention was 3.67 years (95%CI 3.41-3.83) for TNFi-combo, 4.14 (3.77-4.62) for TNFi-mono, 2.98 (2.76-3.34) for TCZ-combo and 3.63 years (3.34-5.03) for TCZ-mono. After adjustment for covariates, country and year of treatment initiation stratification, hazards of discontinuation were lower for TCZ-mono (0.60, 95% CI 0.52-0.69) and TCZ-combo (0.66, 95% CI 0.54-0.81) compared to TNFi-combo. Adjusted CDAI evolution was not significantly different between groups. CDAI LDA and remission corrected for attrition were similar between TCZ with or without csDMARDs and TNFi-combo. CONCLUSION: In routine care across 7 European countries, the adjusted drug retention, adjusted CDAI over time and attrition-corrected response proportion for RA patients were similar for bio-naïve patients if treated with TNFi-combo, TCZ-combo or TCZ-mono.
ARBITER Institute of Rheumatology Moscow Russian Federation
BioRx si University Medical Centre Ljubljana Ljubljana Slovenia
Center of Rheumatic Diseases University of Medicine and Pharmacy Bucharest Romania
Department of Rheumatology Diakonhjemmet Hospital Oslo Norway
F Hoffmann La Roche Basel Switzerland
Genentech South San Francisco CA United States
Geneva University Hospitals Division of Rheumatology 1205 Geneva Switzerland
GISEA University Hospital of Bari Bari Italy
Institut of Rheumatology Prague and Clinic of Rheumatology Charles University Prague Czech Republic
Rheumatology Department Hospital Garcia de Orta Almada Portugal
ROB FIN Helsinki University Hospital and Helsinki University Helsinki Finland
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- $a 10.1016/j.semarthrit.2019.06.020 $2 doi
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- $a Lauper, Kim $u Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland. Electronic address: kim.lauper@hcuge.ch
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- $a Comparative effectiveness of TNF inhibitors and tocilizumab with and without conventional synthetic disease-modifying antirheumatic drugs in a pan-European observational cohort of bio-naïve patients with rheumatoid arthritis / $c K. Lauper, D. Mongin, F. Iannone, EK. Kristianslund, TK. Kvien, DC. Nordström, K. Pavelka, M. Pombo-Suarez, Z. Rotar, MJ. Santos, C. Codreanu, G. Lukina, SL. Gale, M. John, Y. Luder, DS. Courvoisier, C. Gabay
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- $a OBJECTIVES: To compare treatment effectiveness in rheumatoid arthritis (RA) patients naïve to biological disease-modifying antirheumatic drugs (bDMARDs) treated with tocilizumab (TCZ) or TNF-inhibitor (TNFi) with (-combo) or without (-mono) conventional synthetic DMARDs (csDMARDs). METHODS: Patients with RA across 7 European registries, naïve to bDMARDs who initiated treatment with TCZ or TNFi from 2009 to 2016 were included. Drug retention rate was analyzed using Kaplan-Meier and Cox models, and CDAI over time by mixed models. The proportions of patients reaching CDAI low disease activity (LDA) and remission after one year were corrected for attrition. RESULTS: 6713 TNFi-combo, 3762 TNFi-mono, 646 TCZ-combo and 384 TCZ-mono were eligible. Crude median retention was 3.67 years (95%CI 3.41-3.83) for TNFi-combo, 4.14 (3.77-4.62) for TNFi-mono, 2.98 (2.76-3.34) for TCZ-combo and 3.63 years (3.34-5.03) for TCZ-mono. After adjustment for covariates, country and year of treatment initiation stratification, hazards of discontinuation were lower for TCZ-mono (0.60, 95% CI 0.52-0.69) and TCZ-combo (0.66, 95% CI 0.54-0.81) compared to TNFi-combo. Adjusted CDAI evolution was not significantly different between groups. CDAI LDA and remission corrected for attrition were similar between TCZ with or without csDMARDs and TNFi-combo. CONCLUSION: In routine care across 7 European countries, the adjusted drug retention, adjusted CDAI over time and attrition-corrected response proportion for RA patients were similar for bio-naïve patients if treated with TNFi-combo, TCZ-combo or TCZ-mono.
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- $a Kristianslund, Eirik K $u Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway
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- $a Santos, Maria J $u Rheumatology Department, Hospital Garcia de Orta, Almada, Portugal
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- $a Codreanu, Catalin $u Center of Rheumatic Diseases, University of Medicine and Pharmacy, Bucharest, Romania
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- $a Lukina, Galina $u ARBITER, Institute of Rheumatology, Moscow, Russian Federation
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- $a Gale, Sara L $u Genentech, South San Francisco, CA, United States
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- $a John, Markus $u F. Hoffmann-La Roche, Basel, Switzerland
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- $a Courvoisier, Delphine S $u Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland
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