Digestive Health

18 November 2010

Biologic therapy limits long-term steroids

An "evolving concept" in the treatment of inflammatory bowel disease is to use biologic agents to obviate long-term treatment with steroids, according to new guidelines.


An "evolving concept" in the treatment of inflammatory bowel disease is to use biologic agents to obviate long-term treatment with steroids, according to new guidelines. However, not all patients with IBD require biologic therapy.

Those and numerous other recommendations are contained in a position statement from the World Congress of Gastroenterology and the European Crohn's and Colitis Organisation, published in the American Journal of Gastroenterology.

The guidelines address when to start biologic therapy for IBD, when to stop, which drug to choose, and how to predict response.

First-line biologic treatment

The lead author, Dr Geert R. D'Haens, with the Academic Medical Centre in Amsterdam, The Netherlands and colleagues advise that availability and patients preference, as well as reimbursement policies, guide the choice of first-line biologic treatment for Crohn's disease (CD). "Infliximab has the most extensive clinical trial data, but other biological agents (adalimumab, certolizumab pegol, and natalizumab) appear to have similar benefits in CD."

Indications for starting one of these agents include steroid-refractory, steroid-dependent, or complex fistulising CD. The authors also point out that "the combination of infliximab with azathioprine is better than monotherapy for induction of remission and mucosal healing up to 1 year in patients who are naive to both agents."

Anti-TNF agents

The likelihood of response to anti-TNF agents is higher in patients with early luminal CD than in those with long-standing disease, the panel states. Also, "Patients with a high CRP have a higher chance of achieving and maintaining response to biological therapy than patients with a low or normal CRP."

The document also lists several contraindications to anti-TNF treatment, including fibrostenotic CD without inflammation, uncontrolled infections, latent TB, and a history of malignancy, severe congestive heart failure, or demyelinating neurologic disease.

In their conclusion, Dr D'Haens and colleagues note, "Loss of response or intolerance to anti-TNF therapy can be managed by optimising dosing regimens, switching anti-TNF agents, or switching class. It is unclear whether these approaches are similarly effective."

They add, "It is also unclear when treatment can be stopped." (Reuters Health/ November 2010)

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