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Recapture and retreatment rates with ixekizumab after withdrawal of therapy in patients with axial spondyloarthritis: results at week 104 from a randomised placebo-controlled withdrawal study.
Landewé, Robert B M; Poddubnyy, Denis; Rahman, Proton; Van den Bosch, Filip E; Bolce, Rebecca; Liu Leage, Soyi; Lisse, Jeffrey R; Park, So Young; Gensler, Lianne.
Afiliación
  • Landewé RBM; Department of Clinical Immunology and Rheumatology, Amsterdam Rheumatology and Immunology Center, Amsterdam, The Netherlands landewe@rlandewe.nl.
  • Poddubnyy D; Rheumatology Department, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Rahman P; German Rheumatism Research Centre, Berlin, Germany.
  • Van den Bosch FE; Division of Rheumatology, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada.
  • Bolce R; Department of Internal Medicine and Pediatrics, Ghent University, Gent, Belgium.
  • Liu Leage S; VIB Center for Inflammation Research, Ghent, Belgium.
  • Lisse JR; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Park SY; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Gensler L; Eli Lilly and Company, Indianapolis, Indiana, USA.
Ann Rheum Dis ; 82(2): 212-216, 2023 Feb.
Article en En | MEDLINE | ID: mdl-36100350
ABSTRACT

OBJECTIVES:

To evaluate the recapture of response with open-label (OL) ixekizumab (IXE) retreatment at week 104 in patients with axial spondyloarthritis who flared after withdrawal of IXE therapy.

METHODS:

COAST-Y (NCT03129100) is a phase III extension study that included a double-blind, placebo-controlled, randomised withdrawal-retreatment period (RWRP). Patients who achieved remission (Ankylosing Spondylitis Disease Activity Score (ASDAS) <1.3 (inactive disease, ID) at least once at week 16 or 20 and <2.1 (low disease activity, LDA) at both visits) were randomised 21 at week 24 to continue IXE or withdraw to placebo. Patients who subsequently flared were switched to OL IXE every 2 or 4 weeks (Q2W or Q4W) at the next visit. The proportions of patients who recaptured ASDAS LDA and ID were summarised for those who experienced flare.

RESULTS:

Of the 155 patients who entered the RWRP (placebo, n=53; IXE Q4W, n=48; IXE Q2W, n=54), 138 (89%) completed week 104. Of the placebo-treated patients (n=53), 28 (53%) experienced a flare during weeks 24-104; of these, 4 (14%) recaptured ASDAS LDA before retreatment with OL IXE, and 23 (82%) recaptured ASDAS LDA and 19 (68%) met ASDAS ID after retreatment. Of the continuously treated IXE patients (n=102), 13 experienced flare; 7 of 13 (54%) recaptured ASDAS LDA before switching to OL IXE retreatment, while 5 of 13 (38%) recaptured ASDAS LDA and 4 of 13 (31%) met ID after switching.

CONCLUSIONS:

Ninety-six per cent of patients withdrawn to placebo recaptured at least ASDAS LDA and 71% recaptured ASDAS ID with IXE retreatment at week 104. This may provide support to patients who may require a brief interruption in therapy.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espondilitis Anquilosante / Anticuerpos Monoclonales Humanizados Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espondilitis Anquilosante / Anticuerpos Monoclonales Humanizados Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article