Dr. Ghosh’s Observed Future Directions
In the future, patients with moderately to severely active UC for whom conventional therapies are failing will benefit from having the option of either anti-TNF or anti-integrin biologic therapies. Further dose optimization of biologic therapies, therapeutic drug monitoring, and more flexible dosing may improve clinical efficacy in the future.28 The appropriate choice of therapy will depend on patient characteristics, patient preference, route of administration, physician expertise, and cost. In addition, the era of precision medicine will continue to evolve and bring with it the possibility of biomarker-guided therapeutic decisions.29
Whether patients with moderately to severely active UC should have to experience conventional treatment failure prior to becoming eligible for first-line biologics needs further investigation and may not turn out to be the case, given the unfavorable safety profiles of the first-line therapies, corticosteroids and thiopurines.8,30 Future development and availability of subcutaneously administered anti-integrin biologics may further expand the choice and suitability of these therapies as first-line biologics, as patient administration preferences are an important factor in therapeutic choice.31,32 Head-to-head comparison studies investigating effectiveness, safety, and patient preference involving anti-TNF and anti-integrin antibodies are needed.
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