PMID- 32920717 OWN - NLM STAT- MEDLINE DCOM- 20210929 LR - 20210929 IS - 1573-2568 (Electronic) IS - 0163-2116 (Linking) VI - 66 IP - 9 DP - 2021 Sep TI - Adding Thiopurine After Loss of Response to Infliximab Versus Early Combination in Treating Crohn's Disease: A Retrospective Study. PG - 3124-3131 LID - 10.1007/s10620-020-06600-z [doi] AB - BACKGROUND: Although combining thiopurine with infliximab (IFX) is considered to improve the clinical efficacy of IFX when treating Crohn's disease (CD), it also increases the risk of adverse events (AEs). We compared the efficacy and safety of delayed thiopurine addition after loss of response (LOR) to IFX with the efficacy and safety of an earlier combination of thiopurine and IFX. METHODS: This retrospective study analyzed patients with CD who started IFX as a first-line biologic at Kyushu University Hospital between June 2002 and July 2018. Patients were assigned to either the early-combination (EC) group, who started IFX and thiopurine simultaneously, or the late-combination (LC) group, who were treated with IFX alone until they developed LOR. We compared the cumulative IFX continuation rates and AE incidence between the two groups. RESULTS: One hundred seventy-six patients were enrolled in this study; 49 were enrolled in the EC group, and 127 were enrolled in the LC group. Disease activity at baseline did not significantly differ between the groups, nor did the cumulative IFX continuation rates differ between the groups (P = 0.30); however, the AE rate was significantly higher in the EC group than in the LC group (38.7% vs. 21.2%; P = 0.02). The severe AE rate was also higher in the EC group than in the LC group (18.3% vs 3.1%; P = 0.001). CONCLUSION: Considering the risk-benefit balance, delayed addition of thiopurine after LOR to IFX might be an alternative strategy when using IFX to treat CD. CI - (c) 2020. Springer Science+Business Media, LLC, part of Springer Nature. FAU - Zeze, Keizo AU - Zeze K AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Hirano, Atsushi AU - Hirano A AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Torisu, Takehiro AU - Torisu T AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. torisut@intmed2.med.kyushu-u.ac.jp. FAU - Esaki, Motohiro AU - Esaki M AD - Division of Gastroenterology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan. FAU - Moriyama, Tomohiko AU - Moriyama T AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Umeno, Junji AU - Umeno J AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Kawasaki, Keisuke AU - Kawasaki K AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Fujioka, Shin AU - Fujioka S AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Fuyuno, Yuta AU - Fuyuno Y AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Matsuno, Yuichi AU - Matsuno Y AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. FAU - Kitazono, Takanari AU - Kitazono T AD - Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. LA - eng PT - Journal Article DEP - 20200913 PL - United States TA - Dig Dis Sci JT - Digestive diseases and sciences JID - 7902782 RN - 0 (Antimetabolites) RN - 0 (Biological Products) RN - B72HH48FLU (Infliximab) RN - E7WED276I5 (Mercaptopurine) RN - MRK240IY2L (Azathioprine) SB - IM CIN - Dig Dis Sci. 2021 Sep;66(9):2851-2852. PMID: 33128112 MH - Adult MH - Antimetabolites/administration & dosage/adverse effects MH - *Azathioprine/administration & dosage/adverse effects MH - Biological Products/administration & dosage/adverse effects MH - *Crohn Disease/diagnosis/drug therapy/epidemiology MH - Drug Monitoring/methods MH - Drug Synergism MH - *Drug Therapy, Combination/adverse effects/methods MH - *Drug-Related Side Effects and Adverse Reactions/diagnosis/etiology MH - Female MH - Humans MH - *Infliximab/administration & dosage/adverse effects MH - Japan/epidemiology MH - Male MH - *Mercaptopurine/administration & dosage/adverse effects MH - Retrospective Studies MH - Risk Assessment MH - Treatment Outcome OTO - NOTNLM OT - Combination therapy OT - Crohn's disease OT - Infliximab OT - Thiopurine EDAT- 2020/09/14 06:00 MHDA- 2021/09/30 06:00 CRDT- 2020/09/13 20:41 PHST- 2020/05/29 00:00 [received] PHST- 2020/09/01 00:00 [accepted] PHST- 2020/09/14 06:00 [pubmed] PHST- 2021/09/30 06:00 [medline] PHST- 2020/09/13 20:41 [entrez] AID - 10.1007/s10620-020-06600-z [pii] AID - 10.1007/s10620-020-06600-z [doi] PST - ppublish SO - Dig Dis Sci. 2021 Sep;66(9):3124-3131. doi: 10.1007/s10620-020-06600-z. Epub 2020 Sep 13.