2017
DOI: 10.1136/annrheumdis-2016-210713
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Efficacy of biological disease-modifying antirheumatic drugs: a systematic literature review informing the 2016 update of the EULAR recommendations for the management of rheumatoid arthritis

Abstract: ObjectivesTo update the evidence for the efficacy of biological disease-modifying antirheumatic drugs (bDMARDs) in patients with rheumatoid arthritis (RA) to inform European League Against Rheumatism (EULAR) Task Force treatment recommendations.MethodsMEDLINE, EMBASE and Cochrane databases were searched for phase III or IV (or phase II, if these studies were lacking) randomised controlled trials (RCTs) published between January 2013 and February 2016. Abstracts from the American College of Rheumatology and EUL… Show more

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Cited by 217 publications
(165 citation statements)
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“…This SLR is an update of the SLR performed previously for the corresponding 2013 update of the RA management recommendations 6. The results of this and two other SLRs2 3 provided the task force with the current state of evidence.…”
Section: Introductionmentioning
confidence: 90%
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“…This SLR is an update of the SLR performed previously for the corresponding 2013 update of the RA management recommendations 6. The results of this and two other SLRs2 3 provided the task force with the current state of evidence.…”
Section: Introductionmentioning
confidence: 90%
“…However, there are no important differences in efficacy across bDMARDs and tsDMARDs 2 3. Therefore, other aspects among which safety may have a more prominent place in decision-making 1.…”
Section: Introductionmentioning
confidence: 99%
“…The results of this and two other systematic literature reviews (SLRs)4 5 provided the task force with the current state of evidence.…”
Section: Introductionmentioning
confidence: 95%
“…Ремиссии через 6 мес от начала терапии стандартными базисными противо-воспалительными препаратами (БПВП), по данным рандомизированных контролируемых исследований (РКИ), достигают лишь 1,6-2,6% больных РА и 7,2-16% пациентов в группах, получающих помимо БПВП то-фацитиниб [2]. По данным РКИ С-EARLY [3], после 10-13 мес приема метотрексата (МТ) ремиссия по кри-териям Европейской антиревматической лиги (EULAR) была достигнута у 15%, а в группе получающих наряду с МТ цертолизумаба пэгол -у 29% больных РА. Извест-но, что 30-40% пациентов с РА, у которых отмечена не-эффективность МТ, не отвечают на ингибиторы фактора некроза опухоли α (ФНОα) [4].…”
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