Upadacitinib monotherapy versus methotrexate monotherapy in methotrexate-naïve Japanese patients with rheumatoid arthritis : a sub-analysis of the Phase 3 SELECT-EARLY study
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , |
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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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 |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/226288 |
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1439-7609 |
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001129962 |
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http://hdl.handle.net/10183/226288 |
dc.language.iso.fl_str_mv |
eng |
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eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Modern rheumatology. Tokyo. Vol. 31, no. 3 (2021), p. 534–542. |
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openAccess |
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