Cargando…

Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study

Our aim was to assess the ability of tocilizumab monotherapy to reduce progressive structural joint damage in rheumatoid arthritis patients at high risk of progression. This study was a subanalysis from a prospective 1-year, multicenter, X-ray-reader-blinded, randomized controlled trial of tocilizum...

Descripción completa

Detalles Bibliográficos
Autores principales: Hashimoto, Jun, Garnero, Patrick, van der Heijde, Désirée, Miyasaka, Nobuyuki, Yamamoto, Kazuhiko, Kawai, Shinichi, Takeuchi, Tsutomu, Yoshikawa, Hideki, Nishimoto, Norihiro
Formato: Texto
Lenguaje:English
Publicado: Springer Japan 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3036807/
https://www.ncbi.nlm.nih.gov/pubmed/20574648
http://dx.doi.org/10.1007/s10165-010-0325-3
_version_ 1782197900730695680
author Hashimoto, Jun
Garnero, Patrick
van der Heijde, Désirée
Miyasaka, Nobuyuki
Yamamoto, Kazuhiko
Kawai, Shinichi
Takeuchi, Tsutomu
Yoshikawa, Hideki
Nishimoto, Norihiro
author_facet Hashimoto, Jun
Garnero, Patrick
van der Heijde, Désirée
Miyasaka, Nobuyuki
Yamamoto, Kazuhiko
Kawai, Shinichi
Takeuchi, Tsutomu
Yoshikawa, Hideki
Nishimoto, Norihiro
author_sort Hashimoto, Jun
collection PubMed
description Our aim was to assess the ability of tocilizumab monotherapy to reduce progressive structural joint damage in rheumatoid arthritis patients at high risk of progression. This study was a subanalysis from a prospective 1-year, multicenter, X-ray-reader-blinded, randomized controlled trial of tocilizumab [Study of Active Controlled Monotherapy Used for Rheumatoid Arthritis, an IL-6 Inhibitor (SAMURAI) trial]. All patients were categorized into two or three groups according to four independent predictive markers for progressive joint damage [urinary C-terminal crosslinking telopeptide (uCTX-II), urinary pyridinoline/deoxypyridinoline (uPYD/DPD) ratio, body mass index (BMI), and joint-space narrowing (JSN) score at baseline]. One-year progression of joint destruction was assessed in high-risk versus low-risk groups receiving tocilizumab monotherapy and compared with patients receiving conventional disease-modifying antirheumatic drugs (DMARDs) (n = 157 and 145, respectively). In patients at high risk of progression of erosion as estimated by high uCTX-II, uPYD/DPD, or low BMI, and at high risk of progression of JSN as estimated by low BMI or high JSN score, the 52-week changes in radiological erosion and JSN, respectively, were significantly less in patients treated with tocilizumab monotherapy compared with those receiving DMARDs for each type of risk factor. In patients at low risk, those receiving tocilizumab also progressed less than those on DMARDs, although the difference did not reach statistical significance. Tocilizumab monotherapy is more effective in reducing radiological progression in patients presenting with risk factors for rapid progression than in low-risk patients. Patients at high risk for progression may benefit more from tocilizumab treatment.
format Text
id pubmed-3036807
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Springer Japan
record_format MEDLINE/PubMed
spelling pubmed-30368072011-03-16 Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study Hashimoto, Jun Garnero, Patrick van der Heijde, Désirée Miyasaka, Nobuyuki Yamamoto, Kazuhiko Kawai, Shinichi Takeuchi, Tsutomu Yoshikawa, Hideki Nishimoto, Norihiro Mod Rheumatol Original Article Our aim was to assess the ability of tocilizumab monotherapy to reduce progressive structural joint damage in rheumatoid arthritis patients at high risk of progression. This study was a subanalysis from a prospective 1-year, multicenter, X-ray-reader-blinded, randomized controlled trial of tocilizumab [Study of Active Controlled Monotherapy Used for Rheumatoid Arthritis, an IL-6 Inhibitor (SAMURAI) trial]. All patients were categorized into two or three groups according to four independent predictive markers for progressive joint damage [urinary C-terminal crosslinking telopeptide (uCTX-II), urinary pyridinoline/deoxypyridinoline (uPYD/DPD) ratio, body mass index (BMI), and joint-space narrowing (JSN) score at baseline]. One-year progression of joint destruction was assessed in high-risk versus low-risk groups receiving tocilizumab monotherapy and compared with patients receiving conventional disease-modifying antirheumatic drugs (DMARDs) (n = 157 and 145, respectively). In patients at high risk of progression of erosion as estimated by high uCTX-II, uPYD/DPD, or low BMI, and at high risk of progression of JSN as estimated by low BMI or high JSN score, the 52-week changes in radiological erosion and JSN, respectively, were significantly less in patients treated with tocilizumab monotherapy compared with those receiving DMARDs for each type of risk factor. In patients at low risk, those receiving tocilizumab also progressed less than those on DMARDs, although the difference did not reach statistical significance. Tocilizumab monotherapy is more effective in reducing radiological progression in patients presenting with risk factors for rapid progression than in low-risk patients. Patients at high risk for progression may benefit more from tocilizumab treatment. Springer Japan 2010-06-24 2011-02 /pmc/articles/PMC3036807/ /pubmed/20574648 http://dx.doi.org/10.1007/s10165-010-0325-3 Text en © Japan College of Rheumatology 2010
spellingShingle Original Article
Hashimoto, Jun
Garnero, Patrick
van der Heijde, Désirée
Miyasaka, Nobuyuki
Yamamoto, Kazuhiko
Kawai, Shinichi
Takeuchi, Tsutomu
Yoshikawa, Hideki
Nishimoto, Norihiro
Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study
title Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study
title_full Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study
title_fullStr Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study
title_full_unstemmed Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study
title_short Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study
title_sort humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and bmi: data from the samurai study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3036807/
https://www.ncbi.nlm.nih.gov/pubmed/20574648
http://dx.doi.org/10.1007/s10165-010-0325-3
work_keys_str_mv AT hashimotojun humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT garneropatrick humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT vanderheijdedesiree humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT miyasakanobuyuki humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT yamamotokazuhiko humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT kawaishinichi humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT takeuchitsutomu humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT yoshikawahideki humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy
AT nishimotonorihiro humanizedantiinterleukin6receptorantibodytocilizumabmonotherapyismoreeffectiveinslowingradiographicprogressioninpatientswithrheumatoidarthritisathighbaselineriskforstructuraldamageevaluatedwithlevelsofbiomarkersradiographyandbmidatafromthesamuraistudy