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Systematic Review and Meta-analysis: Loss of Response and Need for Dose Escalation of Infliximab and Adalimumab in Ulcerative Colitis.
Savelkoul, Edo H J; Thomas, Pepijn W A; Derikx, Lauranne A A P; den Broeder, Nathan; Römkens, Tessa E H; Hoentjen, Frank.
Afiliación
  • Savelkoul EHJ; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Thomas PWA; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Derikx LAAP; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • den Broeder N; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Römkens TEH; Department of Gastroenterology and Hepatology, Jeroen Bosch Ziekenhuis, 's-Hertogenbosch, the Netherlands.
  • Hoentjen F; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, the Netherlands.
Inflamm Bowel Dis ; 29(10): 1633-1647, 2023 10 03.
Article en En | MEDLINE | ID: mdl-36318229
ABSTRACT

BACKGROUND:

Loss of response to infliximab or adalimumab in ulcerative colitis occurs frequently, and dose escalation may aid in regaining clinical benefit. This study aimed to systematically assess the annual loss of response and dose escalation rates for infliximab and adalimumab in ulcerative colitis.

METHODS:

A systematic search was conducted from August 1999 to July 2021 for studies reporting loss of response and dose escalation during infliximab and/or adalimumab use in ulcerative colitis patients with primary response. Annual loss of response, dose escalation rates, and clinical benefit after dose escalation were calculated. Subgroup analyses were performed for studies with 1-year follow-up or less.

RESULTS:

We included 50 unique studies assessing loss of response (infliximab, n = 24; adalimumab, n = 21) or dose escalation (infliximab, n = 21; adalimumab, n = 16). The pooled annual loss of response for infliximab was 10.1% (95% confidence interval [CI], 7.1-14.3) and 13.6% (95% CI, 9.3-19.9) for studies with 1-year follow-up. The pooled annual loss of response for adalimumab was 13.4% (95% CI, 8.2-21.8) and 23.3% (95% CI, 15.4-35.1) for studies with 1-year follow-up. Annual pooled dose escalation rates were 13.8% (95% CI, 8.7-21.7) for infliximab and 21.3% (95% CI, 14.4-31.3) for adalimumab, regaining clinical benefit in 72.4% and 52.3%, respectively.

CONCLUSIONS:

Annual loss of response was 10% for infliximab and 13% for adalimumab, with higher rates during the first year. Annual dose escalation rates were 14% (infliximab) and 21% (adalimumab), with clinical benefit in 72% and 52%, respectively. Uniform definitions are needed to facilitate more robust evaluations.
Annual loss of response in ulcerative colitis was 10% for infliximab and 13% for adalimumab, with higher rates during the first year. Annual dose escalation was higher than loss of response, with clinical benefit for 72% (infliximab) and 52% (adalimumab).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colitis Ulcerosa Tipo de estudio: Systematic_reviews Límite: Humans Idioma: En Revista: Inflamm Bowel Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colitis Ulcerosa Tipo de estudio: Systematic_reviews Límite: Humans Idioma: En Revista: Inflamm Bowel Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos