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Efficacy and Safety of Vedolizumab in Patients with Inflammatory Bowel Disease in Association with Vedolizumab Drug Levels.
Hüttemann, Eva; Muzalyova, Anna; Gröhl, Katharina; Nagl, Sandra; Fleischmann, Carola; Ebigbo, Alanna; Classen, Johanna; Wanzl, Julia; Prinz, Friederike; Mayr, Patrick; Schnoy, Elisabeth.
Afiliação
  • Hüttemann E; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Muzalyova A; Internal Medicine, Kantonsspital St. Gallen, 9007 St. Gallen, Switzerland.
  • Gröhl K; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Nagl S; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Fleischmann C; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Ebigbo A; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Classen J; Department of Gastroenterology, Hepatology and Endocrinology, Klinikum Nürnberg, 90419 Nuremberg, Germany.
  • Wanzl J; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Prinz F; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Mayr P; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
  • Schnoy E; Internal Medicine III, University Hospital Augsburg, 86156 Augsburg, Germany.
J Clin Med ; 13(1)2023 Dec 27.
Article em En | MEDLINE | ID: mdl-38202147
ABSTRACT

BACKGROUND:

Vedolizumab (VDZ) is a well-established and important therapeutic option in the treatment of patients with inflammatory bowel disease (IBD). However, the significance of therapeutic drug monitoring (TDM) with VDZ remains a contradictory field in daily clinical practice. Our study aims to clarify the predictive impact of VDZ drug levels in long-term clinical outcomes in a real-world cohort.

METHODS:

Patients with moderate to severe ulcerative colitis (UC) and Crohn's disease (CD) from a tertiary IBD referral center at the University Hospital Augsburg, Germany, were enrolled in this single-center retrospective data analysis. Clinical and endoscopic data were collected at month 6, month 12, and at the last time of follow-up, and outcomes were correlated with VDZ levels at week 6.

RESULTS:

This study included 95 patients, 68.4% (n = 65) with UC, 24.2% (n = 23) with CD, and 7.4% (n = 7) with indeterminate colitis (CI). Patients with a mean VDZ treatment time of 17.83 months ± 14.56 showed clinical response in 29.5% (n = 28) and clinical remission in 45.3% (n = 43) at the end of the study. Endoscopic response occurred in 20.0% (n = 19) and endoscopic remission in 29.5% (n = 28) at the end of the study. The sustained beneficial effect of VDZ was also reflected in a significant change in biomarker levels. VDZ trough level at week 6 was determined in 48.4% (n = 46) with a mean of 41.79 µg/mL ± 24.58. A significant association between VDZ level at week 6 and both short and long-term outcomes could not be demonstrated. However, numerically higher VDZ levels were seen in patients with endoscopic and clinical improvement at month 6 and at the time of last follow-up.

CONCLUSIONS:

This study demonstrated efficacy and safety for VDZ in a real-world cohort. Although, for some parameters, a clear trend for higher VDZ levels at week 6 was seen, the efficacy of VDZ was not significantly correlated to VDZ level at week 6, which questions the predictive value of VDZ levels in the real world.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Clin Med Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Clin Med Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha