2007
DOI: 10.1136/gut.2006.103564
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Risks and benefits of biologic therapy for inflammatory bowel diseases

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2007
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Cited by 76 publications
(50 citation statements)
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“…Among the most important side effects of the therapy are increased risk for infections and development of malignancies (8,9). However, in clinical practice, acute infusion reactions are the most frequent cause that limits the use of this biologic therapy in children (10).…”
Section: Introductionmentioning
confidence: 99%
“…Among the most important side effects of the therapy are increased risk for infections and development of malignancies (8,9). However, in clinical practice, acute infusion reactions are the most frequent cause that limits the use of this biologic therapy in children (10).…”
Section: Introductionmentioning
confidence: 99%
“…There were no reports of lymphoma development or tuberculosis, but a serious opportunistic infection of the oligodendrocytes by the JC virus called progressive multifocal leukoencephalopathy was reported in 3 out of 3,819 patients treated with the monoclonalantibody natalizumab with, among them, 1 in a Crohn’s disease patient [83, 85]. At present, there is no useful screening strategy available to screen for or to prevent JC virus infection and treatment is available for patients with multiple sclerosis under strict surveillance [53]. …”
Section: Treatment Adverse Eventsmentioning
confidence: 99%
“…Infections requiring antimicrobial agents are seen in 32% of patients, but severe infections in only 4% of the patients in clinical trials [53]. Opportunistic infections, particularly tuberculosis reactivation, have been described within the first 3 months after initiation of therapy, leading to recommendations for tuberculosis screening (purified protein derivative skin test and chest X-ray) prior to infliximab treatment [54].…”
Section: Treatment Adverse Eventsmentioning
confidence: 99%
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“…The chimeric monoclonal antibody infliximab and the human monoclonal antibody adalimumab have proven similar therapeutic efficacy in patients with IBD and have therefore both been approved for the induction and maintenance of remission in IBD patients in most parts of Europe [2,3]. However, about 50% of IBD patients do not respond to treatment with an anti-TNF antibody and there are no reliable predictors for therapeutic success [4,5]. Moreover, anti-TNF therapy may induce severe side effects (opportunistic infections, allergic reactions, skin disorders and lupus-like autoimmunity) and result in a high economic burden, with costs equaling nearly EUR 25,000/patient per year [6].…”
Section: Introductionmentioning
confidence: 99%