Efficacy, safety, and predictors of response to infliximab therapy for ulcerative colitis: A Korean multicenter retrospective study. Issue 12 (December 2013)
- Record Type:
- Journal Article
- Title:
- Efficacy, safety, and predictors of response to infliximab therapy for ulcerative colitis: A Korean multicenter retrospective study. Issue 12 (December 2013)
- Main Title:
- Efficacy, safety, and predictors of response to infliximab therapy for ulcerative colitis: A Korean multicenter retrospective study
- Authors:
- Lee, Kang‐Moon
Jeen, Yoon Tae
Cho, Ju Yeon
Lee, Chang Kyun
Koo, Ja‐Seol
Park, Dong Il
Im, Jong Pil
Park, Soo Jung
Kim, You Sun
Kim, Tae Oh
Lee, Suck‐Ho
Jang, Byung Ik
Kim, Ji Won
Park, Young Sook
Kim, Eun‐Soo
Choi, Chang Hwan
Kim, Hyo Jong - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12324-sec-0001" sec-type="section"> <title>Background/Aims</title> <p>Infliximab is currently used for the treatment of moderate‐to‐severe ulcerative colitis (UC) with an inadequate response to conventional agents. The efficacy and safety of infliximab in Korean patients with UC were assessed.</p> </sec> <sec id="jgh12324-sec-0002" sec-type="section"> <title>Methods</title> <p>This was a retrospective multicenter study including all adult patients who received at least one infliximab infusion for UC. Short‐ and long‐term clinical outcomes and adverse events of infliximab therapy were evaluated, and predictors of response were identified.</p> </sec> <sec id="jgh12324-sec-0003" sec-type="section"> <title>Results</title> <p>A total of 134 UC patients were included. The indications for infliximab therapy were acute severe UC in 28%, steroid‐dependency in 38%, and steroid‐refractoriness in 33%, respectively. The rates of clinical response and remission were 87% and 45% at week 8. In multivariate analysis, we found significant predictors of clinical remission at week 8: immunomodulator‐naïve (odds ratio [OR] = 4.89, 95% confidence interval [CI]: 1.44–16.66, <italic>P</italic> = 0.01), hemoglobin ≥ 11.5 g/dL (OR = 4.47, 95% CI: 1.48–13.45, <italic>P</italic> = 0.008), C‐reactive protein ≥ 3 mg/dL (OR = 4.77, 95% CI: 1.43–15.94, <italic>P</italic> = 0.01), and response at week 2 (OR = 20.54, 95% CI: 2.40–175.71,<abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12324-sec-0001" sec-type="section"> <title>Background/Aims</title> <p>Infliximab is currently used for the treatment of moderate‐to‐severe ulcerative colitis (UC) with an inadequate response to conventional agents. The efficacy and safety of infliximab in Korean patients with UC were assessed.</p> </sec> <sec id="jgh12324-sec-0002" sec-type="section"> <title>Methods</title> <p>This was a retrospective multicenter study including all adult patients who received at least one infliximab infusion for UC. Short‐ and long‐term clinical outcomes and adverse events of infliximab therapy were evaluated, and predictors of response were identified.</p> </sec> <sec id="jgh12324-sec-0003" sec-type="section"> <title>Results</title> <p>A total of 134 UC patients were included. The indications for infliximab therapy were acute severe UC in 28%, steroid‐dependency in 38%, and steroid‐refractoriness in 33%, respectively. The rates of clinical response and remission were 87% and 45% at week 8. In multivariate analysis, we found significant predictors of clinical remission at week 8: immunomodulator‐naïve (odds ratio [OR] = 4.89, 95% confidence interval [CI]: 1.44–16.66, <italic>P</italic> = 0.01), hemoglobin ≥ 11.5 g/dL (OR = 4.47, 95% CI: 1.48–13.45, <italic>P</italic> = 0.008), C‐reactive protein ≥ 3 mg/dL (OR = 4.77, 95% CI: 1.43–15.94, <italic>P</italic> = 0.01), and response at week 2 (OR = 20.54, 95% CI: 2.40–175.71, <italic>P</italic> = 0.006). Long‐term clinical response and remission rates were 71% and 52%, respectively, and mucosal healing was the only factor influencing long‐term response. Adverse events related to infliximab occurred in 15% of patients, and most of them were mild and transient.</p> </sec> <sec id="jgh12324-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Infliximab is effective and safe in the treatment of active UC in Korea. No history of previous immunomodulator use and high baseline C‐reactive protein are independent predictors of good response.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of gastroenterology and hepatology. Volume 28:Issue 12(2013:Dec.)
- Journal:
- Journal of gastroenterology and hepatology
- Issue:
- Volume 28:Issue 12(2013:Dec.)
- Issue Display:
- Volume 28, Issue 12 (2013)
- Year:
- 2013
- Volume:
- 28
- Issue:
- 12
- Issue Sort Value:
- 2013-0028-0012-0000
- Page Start:
- 1829
- Page End:
- 1833
- Publication Date:
- 2013-12
- Subjects:
- Gastroenterology -- Periodicals
Digestive organs -- Diseases -- Periodicals
Liver -- Diseases -- Periodicals
Gastroenterology -- Periodicals
Liver Diseases -- Periodicals
616.33 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1440-1746 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/jgh ↗ - DOI:
- 10.1111/jgh.12324 ↗
- Languages:
- English
- ISSNs:
- 0815-9319
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4987.615000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3350.xml