Early vedolizumab trough levels at induction in inflammatory bowel disease patients with treatment failure during maintenance.


Journal

European journal of gastroenterology & hepatology
ISSN: 1473-5687
Titre abrégé: Eur J Gastroenterol Hepatol
Pays: England
ID NLM: 9000874

Informations de publication

Date de publication:
04 2019
Historique:
pubmed: 24 1 2019
medline: 25 6 2019
entrez: 24 1 2019
Statut: ppublish

Résumé

Vedolizumab (VDZ) is effective as an induction and maintenance treatment for Crohn's disease and ulcerative colitis, but, as observed with antitumour necrosis factor-α (anti-TNFα) agents, some patients are nonetheless experiencing loss of response. The aim of this study was to investigate the impact of the pharmacokinetics of VDZ during induction on long-term treatment response. This study focused on a single cohort of 103 inflammatory bowel disease patients treated with VDZ. VDZ trough levels (TLs) were measured by enzyme-linked immunosorbent assay (n=536 samples), and thereafter correlated to clinical, biological, endoscopic and serological data. For patients exposed previously to infliximab, antibodies to infliximab were measured at baseline. On the basis of the outcome at the end of follow-up, patients were then categorized into long-term response, optimized and treatment failure groups. During VDZ induction, at week 6, inflammatory bowel disease patients with long-term response had higher TLs compared with patients in the treatment failure group (33 vs. 24 µg/ml, P=0.02). A cut-off TL of 28 µg/ml predicted a sustained response in the follow-up with an area under curve of 0.723 (95% confidence interval=0.567-0.878, P=0.02). Patients with mucosal healing in maintenance had higher TLs at week 6 (41.65 µg/ml) compared with patients with mild (26 µg/ml) or severe endoscopic activity (20.8 µg/ml), P=0.009. Positive perinuclear antineutrophil cytoplasmic antibody serology was associated with lower TLs. Patients previously exposed to anti-TNFα had lower TLs than naive patients (22.5 vs. 36 µg/ml, P=0.03) without any impact of detectable antibodies to infliximab. Finally, the presence of an immunomodulator at induction did not impact on VDZ TLs at induction. We confirmed that a drug exposure-efficacy association was found early on at induction. This study emphasizes that previous exposure to anti-TNFα and positive perinuclear antineutrophil cytoplasmic antibody serology are important factors influencing VDZ TLs at induction.

Sections du résumé

BACKGROUND
Vedolizumab (VDZ) is effective as an induction and maintenance treatment for Crohn's disease and ulcerative colitis, but, as observed with antitumour necrosis factor-α (anti-TNFα) agents, some patients are nonetheless experiencing loss of response.
OBJECTIVE
The aim of this study was to investigate the impact of the pharmacokinetics of VDZ during induction on long-term treatment response.
PATIENTS AND METHODS
This study focused on a single cohort of 103 inflammatory bowel disease patients treated with VDZ. VDZ trough levels (TLs) were measured by enzyme-linked immunosorbent assay (n=536 samples), and thereafter correlated to clinical, biological, endoscopic and serological data. For patients exposed previously to infliximab, antibodies to infliximab were measured at baseline. On the basis of the outcome at the end of follow-up, patients were then categorized into long-term response, optimized and treatment failure groups.
RESULTS
During VDZ induction, at week 6, inflammatory bowel disease patients with long-term response had higher TLs compared with patients in the treatment failure group (33 vs. 24 µg/ml, P=0.02). A cut-off TL of 28 µg/ml predicted a sustained response in the follow-up with an area under curve of 0.723 (95% confidence interval=0.567-0.878, P=0.02). Patients with mucosal healing in maintenance had higher TLs at week 6 (41.65 µg/ml) compared with patients with mild (26 µg/ml) or severe endoscopic activity (20.8 µg/ml), P=0.009. Positive perinuclear antineutrophil cytoplasmic antibody serology was associated with lower TLs. Patients previously exposed to anti-TNFα had lower TLs than naive patients (22.5 vs. 36 µg/ml, P=0.03) without any impact of detectable antibodies to infliximab. Finally, the presence of an immunomodulator at induction did not impact on VDZ TLs at induction.
CONCLUSION
We confirmed that a drug exposure-efficacy association was found early on at induction. This study emphasizes that previous exposure to anti-TNFα and positive perinuclear antineutrophil cytoplasmic antibody serology are important factors influencing VDZ TLs at induction.

Identifiants

pubmed: 30672828
doi: 10.1097/MEG.0000000000001356
doi:

Substances chimiques

Antibodies, Antineutrophil Cytoplasmic 0
Antibodies, Monoclonal, Humanized 0
Biomarkers 0
Gastrointestinal Agents 0
Tumor Necrosis Factor-alpha 0
vedolizumab 9RV78Q2002

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

478-485

Auteurs

Claire Liefferinckx (C)

Laboratory of Experimental Gastroenterology, Université libre de Bruxelles.
Department of Gastroenterology, Erasme Hospital, Brussels.

Charlotte Minsart (C)

Laboratory of Experimental Gastroenterology, Université libre de Bruxelles.
Department of Gastroenterology, Erasme Hospital, Brussels.

Anneline Cremer (A)

Laboratory of Experimental Gastroenterology, Université libre de Bruxelles.
Department of Gastroenterology, Erasme Hospital, Brussels.

Leila Amininejad (L)

Department of Gastroenterology, Erasme Hospital, Brussels.

Vjola Tafciu (V)

Laboratory of Experimental Gastroenterology, Université libre de Bruxelles.

Eric Quertinmont (E)

Laboratory of Experimental Gastroenterology, Université libre de Bruxelles.

Sophie Tops (S)

Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Belgium.

Jacques Devière (J)

Laboratory of Experimental Gastroenterology, Université libre de Bruxelles.
Department of Gastroenterology, Erasme Hospital, Brussels.

Ann Gils (A)

Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Belgium.

André van Gossum (A)

Department of Gastroenterology, Erasme Hospital, Brussels.

Denis Franchimont (D)

Laboratory of Experimental Gastroenterology, Université libre de Bruxelles.
Department of Gastroenterology, Erasme Hospital, Brussels.

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Classifications MeSH