Data di Pubblicazione:
2018
Abstract:
The advent of anti-tumour necrosis factor (TNF) drugs for rheumatoid arthritis (RA) or spondyloarthritis (SpA)
has revolutionised the approach to patientswith active disease who do not respond to conventional therapy. Although
there are differences in their structure,morphology, pharmacokinetic properties and activity, all anti-TNF
drugs ultimately neutralise the TNFα pathway of inflammation. However, despite their similar clinical efficacy,
there are disagreements concerning drug survival and safety, with systematic reviews and meta-analyses
confirming one result or the other. The fact that 20–30% of patients fail to respond to TNFα inhibitors indicates
the possibility of primary resistance or the development of an immune response to the drugs themselves,
which may act as antigens. The overall benefit of switching to another anti-TNF drug or a biological agent with
a different mechanism of action, may be a valuable option in individual patients. There are few data concerning
the use of anti-TNF drugs in patientswith SpA but it seems that there are fewer adverse advents and higher drug
survival in comparison with patients with RA.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
Anti-TNF drugs; Drug survival; Rheumatoid arthritis; Safety; Spondyloarthritis; Immunology and Allergy; Immunology
Elenco autori:
Rubbert-Roth, Andrea; Atzeni, Fabiola; Masala, Ignazio Francesco; Caporali, Roberto; Montecucco, Carlomaurizio; Sarzi-Puttini, Piercarlo
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