Systematic review with meta-analysis: the efficacy of a second anti-TNF in patients with inflammatory bowel disease whose previous anti-TNF treatment has failed
- PMID: 25652884
- DOI: 10.1111/apt.13083
Systematic review with meta-analysis: the efficacy of a second anti-TNF in patients with inflammatory bowel disease whose previous anti-TNF treatment has failed
Abstract
Background: One-third of patients with Crohn's disease (CD) or ulcerative colitis (UC) receiving anti-TNFs do not respond to treatment, and a relevant proportion experience loss of response or intolerance.
Aim: To investigate the efficacy and safety of a second anti-TNF agent after primary/secondary failure or intolerance to a first drug.
Inclusion criteria: studies evaluating the efficacy of infliximab (IFX), adalimumab (ADA) and certolizumab-pegol (CZP) as the second anti-TNF in CD or UC.
Search strategy: Bibliographical searches (PubMed/Embase).
Data synthesis: percentage of response/remission; the meta-analysis was performed using the inverse variance method.
Results: We included 46 studies (37 CD, 8 UC, 1 pouchitis). The CD studies comprised 32 switching IFX→ADA, 4 IFX→CZP and 1 ADA→IFX. Overall, the second anti-TNF after the failure of IFX in CD induced remission in 43% and response in 63% of patients. The remission rate was higher when the reason to withdraw the first anti-TNF was intolerance (61%) than after secondary (45%) or primary failure (30%); response rates were, respectively, 72%, 62% and 53%. All UC studies switched IFX→ADA, six of them reporting remission rates ranging from 0% to 50%. Adverse events rate ranged from 0% to 81% in CD, most of them mild (serious adverse event 0-21%, discontinuation rate <20%).
Conclusions: The efficacy of a second anti-TNF in CD patients largely depends on the cause for switching. The remission rate is higher when the reason to withdraw the first anti-TNF is intolerance (61%), compared with secondary (45%) or primary failure (30%). Further studies of switch ADA→IFX are needed to evaluate this strategy. PROSPERO-registry-number: CRD42014012943.
© 2015 John Wiley & Sons Ltd.
Comment in
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Letter: tumour necrosis factor alpha blocker switching--a not so simple pharmacokinetic.Aliment Pharmacol Ther. 2015 Jun;41(12):1302. doi: 10.1111/apt.13212. Aliment Pharmacol Ther. 2015. PMID: 25968153 No abstract available.
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Letter: tumour necrosis factor alpha blocker switching--a not so simple pharmacokinetic. Authors' reply.Aliment Pharmacol Ther. 2015 Jun;41(12):1302-3. doi: 10.1111/apt.13222. Aliment Pharmacol Ther. 2015. PMID: 25968154 No abstract available.
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Letter: switching from one to another anti-tumour necrosis factor alpha agent, and the risks of an overlap of exposure.Aliment Pharmacol Ther. 2016 May;43(9):1019-20. doi: 10.1111/apt.13565. Aliment Pharmacol Ther. 2016. PMID: 27040168 No abstract available.
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Letter: switching from one to another anti-tumour necrosis factor alpha agent, and the risks of an overlap of exposure--authors' reply.Aliment Pharmacol Ther. 2016 May;43(9):1020. doi: 10.1111/apt.13579. Aliment Pharmacol Ther. 2016. PMID: 27040169 No abstract available.
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