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Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial
OBJECTIVE: To report the 2‐year efficacy and safety of tocilizumab (TCZ) in patients with polyarticular‐course juvenile idiopathic arthritis (JIA). METHODS: Patients ages 2–17 years with active polyarticular‐course JIA, in whom treatment with methotrexate was unsuccessful, received 16 weeks of open‐...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986602/ https://www.ncbi.nlm.nih.gov/pubmed/32951358 http://dx.doi.org/10.1002/art.41528 |
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author | Brunner, Hermine I. Ruperto, Nicolino Zuber, Zbigniew Cuttica, Rubén Keltsev, Vladimir Xavier, Ricardo M. Burgos‐Vargas, Ruben Penades, Inmaculada Calvo Silverman, Earl D. Espada, Graciela Zavaler, Manuel Ferrandiz Kimura, Yukiko Duarte, Carolina Job‐Deslandre, Chantal Joos, Rik Douglass, Wendy Wimalasundera, Sunethra Bharucha, Kamal N. Wells, Chris Lovell, Daniel J. Martini, Alberto de Benedetti, Fabrizio |
author_facet | Brunner, Hermine I. Ruperto, Nicolino Zuber, Zbigniew Cuttica, Rubén Keltsev, Vladimir Xavier, Ricardo M. Burgos‐Vargas, Ruben Penades, Inmaculada Calvo Silverman, Earl D. Espada, Graciela Zavaler, Manuel Ferrandiz Kimura, Yukiko Duarte, Carolina Job‐Deslandre, Chantal Joos, Rik Douglass, Wendy Wimalasundera, Sunethra Bharucha, Kamal N. Wells, Chris Lovell, Daniel J. Martini, Alberto de Benedetti, Fabrizio |
author_sort | Brunner, Hermine I. |
collection | PubMed |
description | OBJECTIVE: To report the 2‐year efficacy and safety of tocilizumab (TCZ) in patients with polyarticular‐course juvenile idiopathic arthritis (JIA). METHODS: Patients ages 2–17 years with active polyarticular‐course JIA, in whom treatment with methotrexate was unsuccessful, received 16 weeks of open‐label intravenous TCZ in part 1 (once every 4 weeks: 8 mg/kg or 10 mg/kg for body weight [BW] <30 kg; 8 mg/kg for BW ≥30 kg). Assessments were based on the JIA–American College of Rheumatology (ACR) response (defined as percentage of improvement in ≥3 of the 6 JIA core response variables [CRVs]). Patients with at least a JIA‐ACR30 response (defined as ≥30% improvement in ≥3 of the 6 JIA CRVs without worsening in >1 of the remaining JIA CRVs by >30%) at week 16 were randomly assigned (1:1) to receive TCZ or placebo in part 2. Patients remained in part 2 until either week 40 or the occurrence of JIA flare. Upon starting part 3, all patients received open‐label TCZ. At week 104 of the study, efficacy was assessed using JIA‐ACR50/70/90 response rates (defined as 50%, 70%, or 90% improvement, respectively), achievement of inactive disease, and the Juvenile Arthritis Disease Activity Score in 71 joints (JADAS‐71). Safety was assessed in the all‐exposure population per 100 patient‐years of exposure. RESULTS: Overall, 188 patients entered part 1, 166 patients entered part 2, and 160 patients entered part 3. By week 104, among the 188 patients in the modified intent‐to‐treat group who received TCZ, JIA‐ACR50/70/90 response rates were 80.3%/77.1%/59.6%, respectively, the median JADAS‐71 score decreased from 3.6 at week 40 to 0.7 at week 104, 51.1% of patients had achieved inactive disease, and 31 of 66 patients who had been receiving glucocorticoids discontinued them. Adverse event (AE) and serious AE rates were 406.5 per 100 patient‐years and 11.1 per 100 patient‐years, respectively. The infection rate was 151.4 per 100 patient‐years, and the serious infection rate was 5.2 per 100 patient‐years. CONCLUSION: Patients treated with TCZ for polyarticular‐course JIA showed high‐level disease control for up to 2 years. The TCZ safety profile was consistent with that previously reported. |
format | Online Article Text |
id | pubmed-7986602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79866022021-03-25 Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial Brunner, Hermine I. Ruperto, Nicolino Zuber, Zbigniew Cuttica, Rubén Keltsev, Vladimir Xavier, Ricardo M. Burgos‐Vargas, Ruben Penades, Inmaculada Calvo Silverman, Earl D. Espada, Graciela Zavaler, Manuel Ferrandiz Kimura, Yukiko Duarte, Carolina Job‐Deslandre, Chantal Joos, Rik Douglass, Wendy Wimalasundera, Sunethra Bharucha, Kamal N. Wells, Chris Lovell, Daniel J. Martini, Alberto de Benedetti, Fabrizio Arthritis Rheumatol Pediatric Rheumatology OBJECTIVE: To report the 2‐year efficacy and safety of tocilizumab (TCZ) in patients with polyarticular‐course juvenile idiopathic arthritis (JIA). METHODS: Patients ages 2–17 years with active polyarticular‐course JIA, in whom treatment with methotrexate was unsuccessful, received 16 weeks of open‐label intravenous TCZ in part 1 (once every 4 weeks: 8 mg/kg or 10 mg/kg for body weight [BW] <30 kg; 8 mg/kg for BW ≥30 kg). Assessments were based on the JIA–American College of Rheumatology (ACR) response (defined as percentage of improvement in ≥3 of the 6 JIA core response variables [CRVs]). Patients with at least a JIA‐ACR30 response (defined as ≥30% improvement in ≥3 of the 6 JIA CRVs without worsening in >1 of the remaining JIA CRVs by >30%) at week 16 were randomly assigned (1:1) to receive TCZ or placebo in part 2. Patients remained in part 2 until either week 40 or the occurrence of JIA flare. Upon starting part 3, all patients received open‐label TCZ. At week 104 of the study, efficacy was assessed using JIA‐ACR50/70/90 response rates (defined as 50%, 70%, or 90% improvement, respectively), achievement of inactive disease, and the Juvenile Arthritis Disease Activity Score in 71 joints (JADAS‐71). Safety was assessed in the all‐exposure population per 100 patient‐years of exposure. RESULTS: Overall, 188 patients entered part 1, 166 patients entered part 2, and 160 patients entered part 3. By week 104, among the 188 patients in the modified intent‐to‐treat group who received TCZ, JIA‐ACR50/70/90 response rates were 80.3%/77.1%/59.6%, respectively, the median JADAS‐71 score decreased from 3.6 at week 40 to 0.7 at week 104, 51.1% of patients had achieved inactive disease, and 31 of 66 patients who had been receiving glucocorticoids discontinued them. Adverse event (AE) and serious AE rates were 406.5 per 100 patient‐years and 11.1 per 100 patient‐years, respectively. The infection rate was 151.4 per 100 patient‐years, and the serious infection rate was 5.2 per 100 patient‐years. CONCLUSION: Patients treated with TCZ for polyarticular‐course JIA showed high‐level disease control for up to 2 years. The TCZ safety profile was consistent with that previously reported. John Wiley and Sons Inc. 2021-02-09 2021-03 /pmc/articles/PMC7986602/ /pubmed/32951358 http://dx.doi.org/10.1002/art.41528 Text en © 2020 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Pediatric Rheumatology Brunner, Hermine I. Ruperto, Nicolino Zuber, Zbigniew Cuttica, Rubén Keltsev, Vladimir Xavier, Ricardo M. Burgos‐Vargas, Ruben Penades, Inmaculada Calvo Silverman, Earl D. Espada, Graciela Zavaler, Manuel Ferrandiz Kimura, Yukiko Duarte, Carolina Job‐Deslandre, Chantal Joos, Rik Douglass, Wendy Wimalasundera, Sunethra Bharucha, Kamal N. Wells, Chris Lovell, Daniel J. Martini, Alberto de Benedetti, Fabrizio Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial |
title | Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial |
title_full | Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial |
title_fullStr | Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial |
title_full_unstemmed | Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial |
title_short | Efficacy and Safety of Tocilizumab for Polyarticular‐Course Juvenile Idiopathic Arthritis in the Open‐Label Two‐Year Extension of a Phase III Trial |
title_sort | efficacy and safety of tocilizumab for polyarticular‐course juvenile idiopathic arthritis in the open‐label two‐year extension of a phase iii trial |
topic | Pediatric Rheumatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986602/ https://www.ncbi.nlm.nih.gov/pubmed/32951358 http://dx.doi.org/10.1002/art.41528 |
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