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Volume 3, Issue 12, Pages 1167-1179 (December 2005)


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Advances in Gastrointestinal Pharmacotherapy

David C. Metz, Nimish Vakil§, Emmet B. Keeffe, Gary R. LichtensteinCorresponding Author Informationemail address

published online 21 November 2005.

The medical management of patients with gastrointestinal diseases is advancing rapidly. At a recent symposium held during Digestive Disease Week in Chicago in May of 2005, specific attention was given to the future prospects for medical management of 3 common gastrointestinal disease areas: antisecretory therapy, chronic hepatitis C, and inflammatory bowel disease. Antisecretory approaches include drug combinations including a proton pump inhibitor, potassium competitive acid blockers, and antigastrin agents. The latter two classes are still experimental, but the former combinations have potential to enhance the highly effective agents currently available. The focus of treatment advances in chronic hepatitis C in the immediate future is the discovery of more effective treatment regimens for nonresponders to prior therapy, who are becoming the largest group of patients seeking treatment of hepatitis C. The combination of peginterferon with ribavirin results in 6%–15% sustained virologic response rates in patients who were prior nonresponders to standard interferon plus ribavirin. Newer strategies to eradicate hepatitis C virus infection using different interferons, such as interferon alfacon-1 or higher doses of peginterferon, or long-term maintenance peginterferon, are undergoing study and show promise based on data from preliminary studies. Several immunomodulators have promise in inflammatory bowel disease, although the risk-benefit ratio and costs of therapy require evaluation. Nevertheless, the success of new biologics such as anti-TNFα agents augurs well for effective future therapies.

 Division of Gastroenterology, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania

 University of Wisconsin Medical School, Madison, Wisconsin

§ Marquette University College of Health Sciences, Milwaukee, Wisconsin

 Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California

Corresponding Author InformationAddress requests for reprints to: Gary R. Lichtenstein, MD, Division of Gastroenterology, 3rd Floor Ravdin, 3400 Spruce Street, Philadelphia, Pennsylvania 19104; fax: (215) 349-5915.

 Dr Metz has received grant support, been a Consultant for, and/or has served on the Speakers Bureau for Altana, TAP, AstraZeneca, Wyeth, Novartis, Santarus, Merck, and Pfizer. Dr Vakil has received research support or been a Consultant for Altana, AstraZeneca, Pfizer, TAP, Eisai, Orexo, Santarus, and Novartis. Dr Keeffe has received grant support from Roche, served on the Advisory Board for Roche and Intermune, and served on the Speakers Bureau for Roche and Schering. Dr Lichtenstein has received research support, been a Consultant for, and/or has served on the Speakers Bureau for Abbott, AstraZeneca, Axcan, Berlex, Celgene, Celltech, Centocor, Elan, Faro, Genetics Institute, Human Genome Sciences, Inkine, Intesco, ISIS, Millenium Pharmaceuticals, Otsuka, Proctor and Gamble, Prometheus Laboratories, Protein Design Labs, Protomed Scientific, Salix, Schering-Plough, Serono, Shire, Smith Kline Beecham, Solvay, Synta, UCB, and Wyeth. He has also received an honorarium from Falk Pharma.

PII: S1542-3565(05)00895-5


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