Doubling the single-dose infusion rate of tocilizumab in rheumatoid arthritis is safe and efficacious.
| dc.contributor.author | Lindegaard, H M | |
| dc.contributor.author | Johansen, P | |
| dc.contributor.author | Gröndal, G | |
| dc.contributor.author | Jensen, E C | |
| dc.contributor.author | Juul, L | |
| dc.contributor.author | Schlemmer, A M | |
| dc.contributor.author | Agular, B | |
| dc.contributor.author | Hansen, Imj | |
| dc.date.accessioned | 2016-06-30T14:19:44Z | |
| dc.date.available | 2016-06-30T14:19:44Z | |
| dc.date.issued | 2016-07 | |
| dc.date.submitted | 2016 | |
| dc.identifier.citation | Doubling the single-dose infusion rate of tocilizumab in rheumatoid arthritis is safe and efficacious. 2016, 45 (4):262-6 Scand. J. Rheumatol. | en |
| dc.identifier.issn | 1502-7732 | |
| dc.identifier.pmid | 26727655 | |
| dc.identifier.doi | 10.3109/03009742.2015.1112030 | |
| dc.identifier.uri | http://hdl.handle.net/2336/615145 | |
| dc.description | To access publisher's full text version of this article click on the hyperlink at the bottom of the page | en |
| dc.description.abstract | To investigate the impact of enhanced infusion rate of tocilizumab on the occurrence of infusion reactions, overall safety, and efficacy in rheumatoid arthritis (RA). | |
| dc.description.abstract | We conducted a 24-week multicentre, open-label, randomized parallel group study comparing adverse event (AE) and effect profiles following tocilizumab IV 8 mg/kg every 4 weeks over 31 min vs. standard 60-min infusions in patients with RA and an inadequate clinical response to disease-modifying anti-rheumatic drugs (DMARDs) and/or tumour necrosis factor (TNF)-α inhibitors. | |
| dc.description.abstract | A total of 47 patients were enrolled in the study and randomized to fast infusions (n = 25) and controls (n = 22). Incidences of infusion reactions were similar between the two groups, neither of them leading to withdrawal. Likewise, the incidence of additional AEs did not differ between the treatment arms. Two serious adverse events (SAEs) were reported, in the control group. Four patients withdrew due to AEs, two from each arm. Efficacy at week 24 was comparable between groups. | |
| dc.description.abstract | In RA, monthly tocilizumab infusions of 8 mg/kg provided over 31 or 60 min during 24 weeks did not differ concerning safety or efficacy. | |
| dc.language.iso | en | en |
| dc.publisher | Taylor & Francis | en |
| dc.relation.url | http://dx.doi.org/ 10.3109/03009742.2015.1112030 | en |
| dc.relation.url | http://www.tandfonline.com/doi/pdf/10.3109/03009742.2015.1112030 | en |
| dc.rights | Archived with thanks to Scandinavian journal of rheumatology | en |
| dc.subject | Liðagigt | en |
| dc.subject | Lyfjameðferð | en |
| dc.subject | RHE12 | |
| dc.subject.mesh | Arthritis, Rheumatoid/drug therapy | en |
| dc.subject.mesh | Antibodies, Monoclonal, Humanized | en |
| dc.subject.mesh | Treatment Outcome | en |
| dc.subject.mesh | Safety | en |
| dc.subject.mesh | Antirheumatic Agents/therapeutic use | en |
| dc.title | Doubling the single-dose infusion rate of tocilizumab in rheumatoid arthritis is safe and efficacious. | en |
| dc.type | Article | en |
| dc.contributor.department | [ 1 ] Odense Univ Hosp, Dept Rheumatol, Sdr Blvd 29, DK-5000 Odense, Denmark [ 2 ] Holbaek Cent Hosp, Holbaek, Denmark [ 3 ] Landspitali Univ Hosp, Reykjavik, Iceland Organization-Enhanced Name(s) Landspitali National University Hospital [ 4 ] Frederiksberg Univ Hosp, Frederiksberg, Denmark [ 5 ] Gentofte Univ Hosp, Gentofte, Denmark [ 6 ] Aalborg Univ Hosp, Aalborg, Denmark [ 7 ] Roche AS, Hvidovre, Denmark [ 8 ] Svendborg Hosp, Svendborg, Denmark | en |
| dc.identifier.journal | Scandinavian journal of rheumatology | en |
| dc.rights.access | Landspitali Access - LSH-aðgangur | en |
| html.description.abstract | To investigate the impact of enhanced infusion rate of tocilizumab on the occurrence of infusion reactions, overall safety, and efficacy in rheumatoid arthritis (RA). | |
| html.description.abstract | We conducted a 24-week multicentre, open-label, randomized parallel group study comparing adverse event (AE) and effect profiles following tocilizumab IV 8 mg/kg every 4 weeks over 31 min vs. standard 60-min infusions in patients with RA and an inadequate clinical response to disease-modifying anti-rheumatic drugs (DMARDs) and/or tumour necrosis factor (TNF)-α inhibitors. | |
| html.description.abstract | A total of 47 patients were enrolled in the study and randomized to fast infusions (n = 25) and controls (n = 22). Incidences of infusion reactions were similar between the two groups, neither of them leading to withdrawal. Likewise, the incidence of additional AEs did not differ between the treatment arms. Two serious adverse events (SAEs) were reported, in the control group. Four patients withdrew due to AEs, two from each arm. Efficacy at week 24 was comparable between groups. | |
| html.description.abstract | In RA, monthly tocilizumab infusions of 8 mg/kg provided over 31 or 60 min during 24 weeks did not differ concerning safety or efficacy. |