Safety, efficacy and pharmacokinetics of vedolizumab in patients with simultaneous exposure to an anti-tumour necrosis factor

被引:11
作者
Ben-Horin, S. [1 ,2 ]
Ungar, B. [1 ]
Kopylov, U. [1 ]
Lahat, A. [1 ]
Yavzori, M. [1 ]
Fudim, E. [1 ]
Picard, O. [1 ]
Peled, Y. [3 ,4 ]
Eliakim, R. [1 ]
Del Tedesco, E. [5 ]
Paul, S. [5 ]
Roblin, X. [5 ]
机构
[1] Tel Aviv Univ, Sackler Sch Med, Dept Gastroenterol, Sheba Med Ctr Tel Hashomer, Tel Aviv, Israel
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[3] Sheba Med Ctr, Cardiol Dept, Ramat Gan, Israel
[4] Tel Aviv Univ, Tel Aviv, Israel
[5] Univ Hosp St Etienne, Dept Gastroenterol, St Etienne, France
关键词
INFLAMMATORY-BOWEL-DISEASE; CROHNS-DISEASE; COMBINATION THERAPY; ULCERATIVE-COLITIS; INDUCTION THERAPY; RHEUMATOID-ARTHRITIS; MAINTENANCE THERAPY; MULTICENTER COHORT; INFLIXIMAB; AZATHIOPRINE;
D O I
10.1111/apt.14567
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Data on combination-biologic treatment in (IBD) are still scant. Aim: To explore outcomes of patients co-exposed to anti-TNF and vedolizumab. Methods: Patients starting vedolizumab having measurable anti-TNF levels after recently stopping adalimumab/infliximab (VDZ-aTNF' group), were compared with control vedolizumab patients in a retrospective 1:2 matched case-control study. Results: Seventy-five patients were included (25 VDZ-aTNF, 50 VDZ). Adverse events were experienced by 9/25 VDZ-aTNF compared to 13/50 VDZ patients (P = 0.4, follow-up 14 weeks in all). Week 14 clinical remission was attained in 10/25 (40%) of VDZ-aTNF patients versus 23/50 (46%) of VDZ patients (OR = 0.8, 95% CI 0.3-2.1, P = 0.6) and clinical response in 19/25 (76%) versus 39/50 (78%) respectively (OR = 0.9, 95% CI 0.3-2.7, P = 0.8). Corticosteroid-free remission and corticosteroid-free response were experienced by 30% and 54%, respectively, of the entire cohort, and were similar between the two groups. Vedolizumab drug concentrations at week 2, 6 and 14 were similar among VDZ-aTNF and VDZ patients (P > 0.5). Multi-variable analysis showed independent association of some vedolizumab drug-levels time-points with baseline albumin and weight, but not with anti-TNF co-exposure. In a prospective study of a separate cohort of patients starting infliximab (n = 12), the percentage of alpha 4 beta 7+ memory T cells, slightly but nonsignificantly increased throughout weeks 0, 2 to 14 (26 +/- 2.3%, 27.8 +/- 2.9%, 29.5 +/- 2.6% respectively, P = 0.06). Conclusions: Vedolizumab/anti-TNF co-exposure did not generate new safety signals during 14-weeks induction, nor did it reduce efficacy or alter vedolizumab pharmacokinetics. These observations may aid the design of future co-biologics trials and also suggest that a deliberate waiting-interval between anti-TNF cessation and subsequent vedolizumab initiation may not be warranted.
引用
收藏
页码:1117 / 1125
页数:9
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