PWE-020 Corticosteroid Dose Reduction with Vedolizumab Treatment of Crohn’s Disease
IntroductionCorticosteroids (CS) can effectively induce remission of Crohn’s disease (CD), but serious side effects prohibit long-term use. Vedolizumab (VDZ) maintenance therapy resulted in a significantly higher percentage of patients with CS-free remission at week 52 versus placebo (PBO) in the GE...
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Veröffentlicht in: | Gut 2016-06, Vol.65 (Suppl 1), p.A147 |
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Zusammenfassung: | IntroductionCorticosteroids (CS) can effectively induce remission of Crohn’s disease (CD), but serious side effects prohibit long-term use. Vedolizumab (VDZ) maintenance therapy resulted in a significantly higher percentage of patients with CS-free remission at week 52 versus placebo (PBO) in the GEMINI 2 study of moderately to severely active CD.1MethodsIn GEMINI 2, patients who responded to VDZ induction therapy at week 6 were re-randomised to PBO or VDZ for 46 weeks. From week 6 onward, patients with clinical response began a CS tapering regimen. With exploratory and post hoc analyses, we characterised CS dose reductions following VDZ therapy in the population of patients on stable CS doses (≤30 mg/day prednisone or equivalent) at baseline (week 0). Median CS dose over time, change from baseline CS dose, and CS-free status at week 52 were summarised overall and by tumour necrosis factor antagonist (anti-TNF) treatment (naïve or failure) history.ResultsAt week 52, 68% of patients with baseline CS use decreased their CS dose with VDZ treatment compared with 62% with PBO (Table). The median CS dose in either treatment group (VDZ or PBO) at week 52 was 5 mg/day. Higher percentages of patients (overall and anti-TNF-naïve) required CS doses of ≤7.5 mg/day with VDZ versus PBO at week 52 (Table). In anti-TNF-naïve patients, the median CS dose at week 52 was 2.7 mg/day with VDZ and 5.0 mg/day with PBO. At week 52, higher percentages of VDZ-treated patients were CS- free for 90 or 180 consecutive days than PBO-treated patients.Abstract PWE-020 Table 1CS Dose changes at week 52Week 52Anti-TNF-NaïveAnti-TNF-FailureOverallPBOn = 29 b VDZa n = 55 b PBOn = 33 b VDZa n = 68 b PBOn = 65 b VDZa n = 127 b No. of Patients (%) CS dose increased 5 (17)3 (5)6 (18)10 (15)11 (17)13 (10) CS dose decreased 18 (62)44 (80)20 (61)38 (56)40 (62)86 (68) CS free 8 (28)25 (45)3 (9)15 (22)12 (18)44 (35) Daily CS dose ≤ 7.5 mg 13 (45)36 (66)14 (42)30 (44)28 (43)70 (55)a VDZ every 4 or 8 weeks.b Patients on CS according to the interactive voice response system (IVRS) at Screening and also on CS for CD according to the case report form at baseline (week 0).ConclusionVDZ maintenance therapy was associated with numerically higher percentages of CS-free patients at week 52 and patients who were CS-free for 90 or 180 days than PBO. Interpretation of these post hoc analyses, including the degree of dose reduction, is limited by differing initiation weeks for CS tapering per patient and small sa |
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ISSN: | 0017-5749 1468-3288 |
DOI: | 10.1136/gutjnl-2016-312388.265 |