Abstract | AIMS: To compare the efficacy and the safety of low-dose (3.5 mg/kg) or standard-dose (5 mg/kg) of infliximab (IFX) for induction and maintenance treatment in Chinese patients with intestinal Behcet's disease (BD), and to identify potential predictors to corticosteroid-free clinical remission at week 30. METHODS: A prospective trial was conducted in 20 patients with moderate-to-severe active intestinal BD, followed up for 30 weeks. Ileocolonoscopic examinations were done at baseline and week 14. A logistic regression model was used to assess the predictors of corticosteroid-free remission at week 30. RESULTS: As the primary end point, steroid-free remission at week 30 was observed in 40% and 60% of patients who received low and standard doses of IFX, respectively (P>0.371). As the secondary end point, the mucosal healing (MH) rates at week 14 were found to be 60% for both low and standard doses of IFX. The clinical response rates at week 14 and 30 were also similar in both groups. Only MH at week 14 predicted steroid-free clinical remission at week 30. CONCLUSIONS: Low-dose of IFX is effective and safe for induction and maintenance therapy in patients with active intestinal BD. MH at week 14 predicted clinical remission at week 30.
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Authors | Jun Zou, Da-Nian Ji, Yan Shen, Jian-Long Guan, Song-Bai Zheng |
Journal | Annals of clinical and laboratory science
(Ann Clin Lab Sci)
Vol. 47
Issue 2
Pg. 171-177
(Mar 2017)
ISSN: 1550-8080 [Electronic] United States |
PMID | 28442519
(Publication Type: Clinical Trial, Journal Article)
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Copyright | © 2017 by the Association of Clinical Scientists, Inc. |
Chemical References |
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Topics |
- Adolescent
- Adult
- Aged
- Asian People
- Behcet Syndrome
(drug therapy, pathology)
- Demography
- Dose-Response Relationship, Drug
- Endpoint Determination
- Female
- Humans
- Infliximab
(administration & dosage, adverse effects, therapeutic use)
- Intestinal Mucosa
(pathology)
- Male
- Middle Aged
- Remission Induction
- Treatment Outcome
- Wound Healing
- Young Adult
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