Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study

Detalhes bibliográficos
Autor(a) principal: Takeuchi, Tsutomu
Data de Publicação: 2021
Outros Autores: Rischmueller, Maureen, Blanco, Ricardo, Xavier, Ricardo Machado, Ueki, Yukitaka, Atsumi, Tatsuya, Su, Chen, Friedman, Alan, Pangan, Aileen L., Strand, Vibeke, Vollenhoven, Ronald F. van
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/226288
Resumo: Objective: To assess upadacitinib monotherapy versus methotrexate (MTX) in MTX-naïve Japanese patients with rheumatoid arthritis (RA) from the Phase 3 SELECT-EARLY study. Methods: Japanese patients were randomized 2:1:1:1 to upadacitinib 7.5, 15, or 30 mg daily or MTX 7.5 mg/week (titrated to 15 mg/week). Efficacy endpoints included the proportion of patients reporting 20% improvement in American College of Rheumatology criteria (ACR20) at week 12 and change from baseline in modified Total Sharp Score (mTSS) at week 24. Other efficacy outcomes were also assessed at weeks 12 and/or 24. Safety was assessed over 24 weeks. Results: Of 138 Japanese patients enrolled, significantly more patients treated with upadacitinib 7.5 and 15 mg, but not 30 mg, reported ACR20 responses versus MTX at week 12. Significantly smaller changes from baseline in mTSS were observed with upadacitinib 15 and 30 mg, but not 7.5 mg, versus MTX at week 24. Upadacitinib demonstrated an acceptable safety profile; herpes zoster occurred in 3.6%, 7.4%, and 7.1% of patients treated with upadacitinib 7.5, 15, and 30 mg, respectively. Conclusion: Similar to the global study population, upadacitinib demonstrated clinical efficacy superior to placebo in the Japanese subpopulation. Among upadacitinib-treated patients, herpes zoster was least common with 7.5 mg.
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spelling Takeuchi, TsutomuRischmueller, MaureenBlanco, RicardoXavier, Ricardo MachadoUeki, YukitakaAtsumi, TatsuyaSu, ChenFriedman, AlanPangan, Aileen L.Strand, VibekeVollenhoven, Ronald F. van2021-08-31T04:19:28Z20211439-7609http://hdl.handle.net/10183/226288001129962Objective: To assess upadacitinib monotherapy versus methotrexate (MTX) in MTX-naïve Japanese patients with rheumatoid arthritis (RA) from the Phase 3 SELECT-EARLY study. Methods: Japanese patients were randomized 2:1:1:1 to upadacitinib 7.5, 15, or 30 mg daily or MTX 7.5 mg/week (titrated to 15 mg/week). Efficacy endpoints included the proportion of patients reporting 20% improvement in American College of Rheumatology criteria (ACR20) at week 12 and change from baseline in modified Total Sharp Score (mTSS) at week 24. Other efficacy outcomes were also assessed at weeks 12 and/or 24. Safety was assessed over 24 weeks. Results: Of 138 Japanese patients enrolled, significantly more patients treated with upadacitinib 7.5 and 15 mg, but not 30 mg, reported ACR20 responses versus MTX at week 12. Significantly smaller changes from baseline in mTSS were observed with upadacitinib 15 and 30 mg, but not 7.5 mg, versus MTX at week 24. Upadacitinib demonstrated an acceptable safety profile; herpes zoster occurred in 3.6%, 7.4%, and 7.1% of patients treated with upadacitinib 7.5, 15, and 30 mg, respectively. Conclusion: Similar to the global study population, upadacitinib demonstrated clinical efficacy superior to placebo in the Japanese subpopulation. Among upadacitinib-treated patients, herpes zoster was least common with 7.5 mg.application/pdfengModern rheumatology. Tokyo. Vol. 31, no. 3 (2021), p. 534–542.Artrite reumatóideMetotrexatoTratamento farmacológicoJapãoDMARDJapanMethotrexateRheumatoid arthritisUpadacitinibUpadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY studyEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001129962.pdf.txt001129962.pdf.txtExtracted Texttext/plain45961http://www.lume.ufrgs.br/bitstream/10183/226288/2/001129962.pdf.txte0819d9106de79c9dcb032dbb7440e24MD52ORIGINAL001129962.pdfTexto completo (inglês)application/pdf1888131http://www.lume.ufrgs.br/bitstream/10183/226288/1/001129962.pdf0c45d744579c08c6a068dbbd8f886a4bMD5110183/2262882021-09-19 04:26:14.408599oai:www.lume.ufrgs.br:10183/226288Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-19T07:26:14Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
title Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
spellingShingle Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
Takeuchi, Tsutomu
Artrite reumatóide
Metotrexato
Tratamento farmacológico
Japão
DMARD
Japan
Methotrexate
Rheumatoid arthritis
Upadacitinib
title_short Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
title_full Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
title_fullStr Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
title_full_unstemmed Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
title_sort Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
author Takeuchi, Tsutomu
author_facet Takeuchi, Tsutomu
Rischmueller, Maureen
Blanco, Ricardo
Xavier, Ricardo Machado
Ueki, Yukitaka
Atsumi, Tatsuya
Su, Chen
Friedman, Alan
Pangan, Aileen L.
Strand, Vibeke
Vollenhoven, Ronald F. van
author_role author
author2 Rischmueller, Maureen
Blanco, Ricardo
Xavier, Ricardo Machado
Ueki, Yukitaka
Atsumi, Tatsuya
Su, Chen
Friedman, Alan
Pangan, Aileen L.
Strand, Vibeke
Vollenhoven, Ronald F. van
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Takeuchi, Tsutomu
Rischmueller, Maureen
Blanco, Ricardo
Xavier, Ricardo Machado
Ueki, Yukitaka
Atsumi, Tatsuya
Su, Chen
Friedman, Alan
Pangan, Aileen L.
Strand, Vibeke
Vollenhoven, Ronald F. van
dc.subject.por.fl_str_mv Artrite reumatóide
Metotrexato
Tratamento farmacológico
Japão
topic Artrite reumatóide
Metotrexato
Tratamento farmacológico
Japão
DMARD
Japan
Methotrexate
Rheumatoid arthritis
Upadacitinib
dc.subject.eng.fl_str_mv DMARD
Japan
Methotrexate
Rheumatoid arthritis
Upadacitinib
description Objective: To assess upadacitinib monotherapy versus methotrexate (MTX) in MTX-naïve Japanese patients with rheumatoid arthritis (RA) from the Phase 3 SELECT-EARLY study. Methods: Japanese patients were randomized 2:1:1:1 to upadacitinib 7.5, 15, or 30 mg daily or MTX 7.5 mg/week (titrated to 15 mg/week). Efficacy endpoints included the proportion of patients reporting 20% improvement in American College of Rheumatology criteria (ACR20) at week 12 and change from baseline in modified Total Sharp Score (mTSS) at week 24. Other efficacy outcomes were also assessed at weeks 12 and/or 24. Safety was assessed over 24 weeks. Results: Of 138 Japanese patients enrolled, significantly more patients treated with upadacitinib 7.5 and 15 mg, but not 30 mg, reported ACR20 responses versus MTX at week 12. Significantly smaller changes from baseline in mTSS were observed with upadacitinib 15 and 30 mg, but not 7.5 mg, versus MTX at week 24. Upadacitinib demonstrated an acceptable safety profile; herpes zoster occurred in 3.6%, 7.4%, and 7.1% of patients treated with upadacitinib 7.5, 15, and 30 mg, respectively. Conclusion: Similar to the global study population, upadacitinib demonstrated clinical efficacy superior to placebo in the Japanese subpopulation. Among upadacitinib-treated patients, herpes zoster was least common with 7.5 mg.
publishDate 2021
dc.date.accessioned.fl_str_mv 2021-08-31T04:19:28Z
dc.date.issued.fl_str_mv 2021
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Modern rheumatology. Tokyo. Vol. 31, no. 3 (2021), p. 534–542.
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