Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)

Detalhes bibliográficos
Autor(a) principal: Sassaki, Ligia Yukie [UNESP]
Data de Publicação: 2022
Outros Autores: Magro, Daniela Oliveira, Saad-Hossne, Rogerio [UNESP], Baima, Julio Pinheiro [UNESP], Flores, Cristina, Correia, Lucianna Motta, Celani, Lívia Medeiros Soares, De Abreu Ferrari, Maria De Lourdes, Zacharias, Patricia, Feitosa, Marley Ribeiro, Dos Santos, Carlos Henrique Marques, De Freitas Lins Neto, Manoel Alvaro, Quaresma, Abel Botelho, De Lima Junior, Sergio Figueiredo, De Vasconcelos, Graciana Bandeira Salgado, Cassol, Ornella Sari, Dos Santos Pinto, Arlene, Kurachi, Gustavo, Goncalves Filho, Francisco de Assis, Gasparini, Rodrigo Galhardi, Furlan, Thaísa Kowalski, Catapani, Wilson Roberto, Coy, Cláudio Saddy Rodrigues, De Souza Menegassi, Vivian, Colombo, Marilia Majeski, Fróes, Renata de Sá Brito, Teixeira, Fabio Vieira, Moraes, Antonio Carlos, Santana, Genoile Oliveira, Parente, José Miguel Luz, Vilela, Eduardo Garcia, Queiroz, Natália Sousa Freitas, Kotze, Paulo Gustavo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/s12876-022-02341-7
http://hdl.handle.net/11449/241093
Resumo: Background: Anti-TNF therapy represented a landmark in medical treatment of ulcerative colitis (UC). There is lack of data on the efficacy and safety of these agents in Brazilian patients. The present study aimed to analyze rates of clinical and endoscopic remission comparatively, between adalimumab (ADA) and infliximab (IFX), in Brazilian patients with UC, and evaluate factors associated with clinical and endoscopic remission after 1 year of treatment. Methods: A national retrospective multicenter study (24 centers) was performed including patients with UC treated with anti-TNF therapy. Outcomes as clinical response and remission, endoscopic remission and secondary loss of response were measured in different time points of the follow-up. Baseline predictive factors of clinical and endoscopic remission at week 52 were evaluated using logistic regression model. Indirect comparisons among groups (ADA and IFX) were performed using Student's t, Pearson χ2 or Fisher's exact test when appropriated, and Kaplan Meier analysis. Results: Overall, 393 patients were included (ADA, n = 111; IFX, n = 282). The mean age was 41.86 ± 13.60 years, 61.58% were female, most patients had extensive colitis (62.40%) and 19.39% had previous exposure to a biological agent. Overall, clinical remission rate was 66.78%, 71.62% and 82.82% at weeks 8, 26 and 52, respectively. Remission rates were higher in the IFX group at weeks 26 (75.12% vs. 62.65%, p < 0.0001) and 52 (65.24% vs. 51.35%, p < 0.0001) when compared to ADA. According to Kaplan–Meier survival curve loss of response was less frequent in the Infliximab compared to Adalimumab group (p = 0.001). Overall, endoscopic remission was observed in 50% of patients at week 26 and in 65.98% at week 52, with no difference between the groups (p = 0.114). Colectomy was performed in 23 patients (5.99%). Age, non-prior exposure to biological therapy, use of IFX and endoscopic remission at week 26 were associated with clinical remission after 52 weeks. Variables associated with endoscopic remission were non-prior exposure to biological therapy, and clinical and endoscopic remission at week 26. Conclusions: IFX was associated with higher rates of clinical remission after 1 year in comparison to ADA. Non-prior exposure to biological therapy and early response to anti-TNF treatment were associated with higher rates of clinical and endoscopic remission.
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spelling Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)AdalimumabAnti-TNF therapyClinical remissionInfliximabUlcerative colitisBackground: Anti-TNF therapy represented a landmark in medical treatment of ulcerative colitis (UC). There is lack of data on the efficacy and safety of these agents in Brazilian patients. The present study aimed to analyze rates of clinical and endoscopic remission comparatively, between adalimumab (ADA) and infliximab (IFX), in Brazilian patients with UC, and evaluate factors associated with clinical and endoscopic remission after 1 year of treatment. Methods: A national retrospective multicenter study (24 centers) was performed including patients with UC treated with anti-TNF therapy. Outcomes as clinical response and remission, endoscopic remission and secondary loss of response were measured in different time points of the follow-up. Baseline predictive factors of clinical and endoscopic remission at week 52 were evaluated using logistic regression model. Indirect comparisons among groups (ADA and IFX) were performed using Student's t, Pearson χ2 or Fisher's exact test when appropriated, and Kaplan Meier analysis. Results: Overall, 393 patients were included (ADA, n = 111; IFX, n = 282). The mean age was 41.86 ± 13.60 years, 61.58% were female, most patients had extensive colitis (62.40%) and 19.39% had previous exposure to a biological agent. Overall, clinical remission rate was 66.78%, 71.62% and 82.82% at weeks 8, 26 and 52, respectively. Remission rates were higher in the IFX group at weeks 26 (75.12% vs. 62.65%, p < 0.0001) and 52 (65.24% vs. 51.35%, p < 0.0001) when compared to ADA. According to Kaplan–Meier survival curve loss of response was less frequent in the Infliximab compared to Adalimumab group (p = 0.001). Overall, endoscopic remission was observed in 50% of patients at week 26 and in 65.98% at week 52, with no difference between the groups (p = 0.114). Colectomy was performed in 23 patients (5.99%). Age, non-prior exposure to biological therapy, use of IFX and endoscopic remission at week 26 were associated with clinical remission after 52 weeks. Variables associated with endoscopic remission were non-prior exposure to biological therapy, and clinical and endoscopic remission at week 26. Conclusions: IFX was associated with higher rates of clinical remission after 1 year in comparison to ADA. Non-prior exposure to biological therapy and early response to anti-TNF treatment were associated with higher rates of clinical and endoscopic remission.Department of Internal Medicine Medical School São Paulo State University (UNESP)Colorectal Surgery Unit University of Campinas UNICAMPDepartment of Surgery Medical School São Paulo State University UnespHospital de Clínicas de Porto AlegreOnofre Lopes Universitary Hospital Federal University of Rio Grande Do NorteMedical School of the Federal University of the Minas GeraisIBD Outpatient Clinics- Colorectal Surgery Unit Catholic University or Paraná PUCPRDepartment of Surgery and Anatomy Ribeirao Preto Medical School University of Sao PauloSurgery Department Universidade Federal de Mato Grosso Do SulFederal University of AlagoasSurgery Universidade Do Oeste de Santa Catarina UNOESCColorectal Surgery Unit João de Barros Barreto University Hospital Federal University of ParáGastroenterologia Fundação Universidade de PernambucoHospital de Clínicas de Passo FundoHospital Universitario Getulio VargasGastroenterology Gastroclinica CascavelDepartment of surgery Faculty of Medicine of São José do Rio Preto, SPSETE - Specialized Medical Center, São PauloGastroenterology Hospital de Clínicas da Universidade Federal do Paraná - HCUFPRGastroenterology Faculdade de Medicina do ABCHospital Universitário Professor Polydoro Ernani de São Thiago da Universidade Federal de Santa Catarina HU-UFSC, Santa CatarinaGastroenterology Hospital Doutor Dório SilvaGastroenterology GastromedGastroSaude Clinic, Sao PauloHospital Copa D’OrBahia State University UNEB, BahiaGastroenterology Division Medical Health Center Federal University of PiauiGastroenterology Hospital of the Federal University of Minas GeraisDepartment of Internal Medicine Medical School São Paulo State University (UNESP)Department of Surgery Medical School São Paulo State University UnespUniversidade Estadual Paulista (UNESP)Universidade Estadual de Campinas (UNICAMP)Hospital de Clínicas de Porto AlegreFederal University of Rio Grande Do NorteMedical School of the Federal University of the Minas GeraisCatholic University or Paraná PUCPRUniversidade de São Paulo (USP)Universidade Federal de Mato Grosso do Sul (UFMS)Federal University of AlagoasUniversidade Do Oeste de Santa Catarina UNOESCUniversidade Federal do Pará (UFPA)Fundação Universidade de PernambucoHospital de Clínicas de Passo FundoHospital Universitario Getulio VargasGastroclinica CascavelFaculty of Medicine of São José do Rio PretoSETE - Specialized Medical CenterUniversidade Federal do Paraná (UFPR)Faculdade de Medicina do ABCUniversidade Federal de Santa Catarina (UFSC)Hospital Doutor Dório SilvaGastromedGastroSaude ClinicHospital Copa D’OrBahia State University UNEBFederal University of PiauiUniversidade Federal de Minas Gerais (UFMG)Sassaki, Ligia Yukie [UNESP]Magro, Daniela OliveiraSaad-Hossne, Rogerio [UNESP]Baima, Julio Pinheiro [UNESP]Flores, CristinaCorreia, Lucianna MottaCelani, Lívia Medeiros SoaresDe Abreu Ferrari, Maria De LourdesZacharias, PatriciaFeitosa, Marley RibeiroDos Santos, Carlos Henrique MarquesDe Freitas Lins Neto, Manoel AlvaroQuaresma, Abel BotelhoDe Lima Junior, Sergio FigueiredoDe Vasconcelos, Graciana Bandeira SalgadoCassol, Ornella SariDos Santos Pinto, ArleneKurachi, GustavoGoncalves Filho, Francisco de AssisGasparini, Rodrigo GalhardiFurlan, Thaísa KowalskiCatapani, Wilson RobertoCoy, Cláudio Saddy RodriguesDe Souza Menegassi, VivianColombo, Marilia MajeskiFróes, Renata de Sá BritoTeixeira, Fabio VieiraMoraes, Antonio CarlosSantana, Genoile OliveiraParente, José Miguel LuzVilela, Eduardo GarciaQueiroz, Natália Sousa FreitasKotze, Paulo Gustavo2023-03-01T20:46:43Z2023-03-01T20:46:43Z2022-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1186/s12876-022-02341-7BMC Gastroenterology, v. 22, n. 1, 2022.1471-230Xhttp://hdl.handle.net/11449/24109310.1186/s12876-022-02341-72-s2.0-85131220737Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Gastroenterologyinfo:eu-repo/semantics/openAccess2024-08-14T17:36:30Zoai:repositorio.unesp.br:11449/241093Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:36:30Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
title Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
spellingShingle Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
Sassaki, Ligia Yukie [UNESP]
Adalimumab
Anti-TNF therapy
Clinical remission
Infliximab
Ulcerative colitis
title_short Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
title_full Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
title_fullStr Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
title_full_unstemmed Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
title_sort Anti-TNF therapy for ulcerative colitis in Brazil: a comparative real-world national retrospective multicentric study from the Brazilian study group of IBD (GEDIIB)
author Sassaki, Ligia Yukie [UNESP]
author_facet Sassaki, Ligia Yukie [UNESP]
Magro, Daniela Oliveira
Saad-Hossne, Rogerio [UNESP]
Baima, Julio Pinheiro [UNESP]
Flores, Cristina
Correia, Lucianna Motta
Celani, Lívia Medeiros Soares
De Abreu Ferrari, Maria De Lourdes
Zacharias, Patricia
Feitosa, Marley Ribeiro
Dos Santos, Carlos Henrique Marques
De Freitas Lins Neto, Manoel Alvaro
Quaresma, Abel Botelho
De Lima Junior, Sergio Figueiredo
De Vasconcelos, Graciana Bandeira Salgado
Cassol, Ornella Sari
Dos Santos Pinto, Arlene
Kurachi, Gustavo
Goncalves Filho, Francisco de Assis
Gasparini, Rodrigo Galhardi
Furlan, Thaísa Kowalski
Catapani, Wilson Roberto
Coy, Cláudio Saddy Rodrigues
De Souza Menegassi, Vivian
Colombo, Marilia Majeski
Fróes, Renata de Sá Brito
Teixeira, Fabio Vieira
Moraes, Antonio Carlos
Santana, Genoile Oliveira
Parente, José Miguel Luz
Vilela, Eduardo Garcia
Queiroz, Natália Sousa Freitas
Kotze, Paulo Gustavo
author_role author
author2 Magro, Daniela Oliveira
Saad-Hossne, Rogerio [UNESP]
Baima, Julio Pinheiro [UNESP]
Flores, Cristina
Correia, Lucianna Motta
Celani, Lívia Medeiros Soares
De Abreu Ferrari, Maria De Lourdes
Zacharias, Patricia
Feitosa, Marley Ribeiro
Dos Santos, Carlos Henrique Marques
De Freitas Lins Neto, Manoel Alvaro
Quaresma, Abel Botelho
De Lima Junior, Sergio Figueiredo
De Vasconcelos, Graciana Bandeira Salgado
Cassol, Ornella Sari
Dos Santos Pinto, Arlene
Kurachi, Gustavo
Goncalves Filho, Francisco de Assis
Gasparini, Rodrigo Galhardi
Furlan, Thaísa Kowalski
Catapani, Wilson Roberto
Coy, Cláudio Saddy Rodrigues
De Souza Menegassi, Vivian
Colombo, Marilia Majeski
Fróes, Renata de Sá Brito
Teixeira, Fabio Vieira
Moraes, Antonio Carlos
Santana, Genoile Oliveira
Parente, José Miguel Luz
Vilela, Eduardo Garcia
Queiroz, Natália Sousa Freitas
Kotze, Paulo Gustavo
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Universidade Estadual de Campinas (UNICAMP)
Hospital de Clínicas de Porto Alegre
Federal University of Rio Grande Do Norte
Medical School of the Federal University of the Minas Gerais
Catholic University or Paraná PUCPR
Universidade de São Paulo (USP)
Universidade Federal de Mato Grosso do Sul (UFMS)
Federal University of Alagoas
Universidade Do Oeste de Santa Catarina UNOESC
Universidade Federal do Pará (UFPA)
Fundação Universidade de Pernambuco
Hospital de Clínicas de Passo Fundo
Hospital Universitario Getulio Vargas
Gastroclinica Cascavel
Faculty of Medicine of São José do Rio Preto
SETE - Specialized Medical Center
Universidade Federal do Paraná (UFPR)
Faculdade de Medicina do ABC
Universidade Federal de Santa Catarina (UFSC)
Hospital Doutor Dório Silva
Gastromed
GastroSaude Clinic
Hospital Copa D’Or
Bahia State University UNEB
Federal University of Piaui
Universidade Federal de Minas Gerais (UFMG)
dc.contributor.author.fl_str_mv Sassaki, Ligia Yukie [UNESP]
Magro, Daniela Oliveira
Saad-Hossne, Rogerio [UNESP]
Baima, Julio Pinheiro [UNESP]
Flores, Cristina
Correia, Lucianna Motta
Celani, Lívia Medeiros Soares
De Abreu Ferrari, Maria De Lourdes
Zacharias, Patricia
Feitosa, Marley Ribeiro
Dos Santos, Carlos Henrique Marques
De Freitas Lins Neto, Manoel Alvaro
Quaresma, Abel Botelho
De Lima Junior, Sergio Figueiredo
De Vasconcelos, Graciana Bandeira Salgado
Cassol, Ornella Sari
Dos Santos Pinto, Arlene
Kurachi, Gustavo
Goncalves Filho, Francisco de Assis
Gasparini, Rodrigo Galhardi
Furlan, Thaísa Kowalski
Catapani, Wilson Roberto
Coy, Cláudio Saddy Rodrigues
De Souza Menegassi, Vivian
Colombo, Marilia Majeski
Fróes, Renata de Sá Brito
Teixeira, Fabio Vieira
Moraes, Antonio Carlos
Santana, Genoile Oliveira
Parente, José Miguel Luz
Vilela, Eduardo Garcia
Queiroz, Natália Sousa Freitas
Kotze, Paulo Gustavo
dc.subject.por.fl_str_mv Adalimumab
Anti-TNF therapy
Clinical remission
Infliximab
Ulcerative colitis
topic Adalimumab
Anti-TNF therapy
Clinical remission
Infliximab
Ulcerative colitis
description Background: Anti-TNF therapy represented a landmark in medical treatment of ulcerative colitis (UC). There is lack of data on the efficacy and safety of these agents in Brazilian patients. The present study aimed to analyze rates of clinical and endoscopic remission comparatively, between adalimumab (ADA) and infliximab (IFX), in Brazilian patients with UC, and evaluate factors associated with clinical and endoscopic remission after 1 year of treatment. Methods: A national retrospective multicenter study (24 centers) was performed including patients with UC treated with anti-TNF therapy. Outcomes as clinical response and remission, endoscopic remission and secondary loss of response were measured in different time points of the follow-up. Baseline predictive factors of clinical and endoscopic remission at week 52 were evaluated using logistic regression model. Indirect comparisons among groups (ADA and IFX) were performed using Student's t, Pearson χ2 or Fisher's exact test when appropriated, and Kaplan Meier analysis. Results: Overall, 393 patients were included (ADA, n = 111; IFX, n = 282). The mean age was 41.86 ± 13.60 years, 61.58% were female, most patients had extensive colitis (62.40%) and 19.39% had previous exposure to a biological agent. Overall, clinical remission rate was 66.78%, 71.62% and 82.82% at weeks 8, 26 and 52, respectively. Remission rates were higher in the IFX group at weeks 26 (75.12% vs. 62.65%, p < 0.0001) and 52 (65.24% vs. 51.35%, p < 0.0001) when compared to ADA. According to Kaplan–Meier survival curve loss of response was less frequent in the Infliximab compared to Adalimumab group (p = 0.001). Overall, endoscopic remission was observed in 50% of patients at week 26 and in 65.98% at week 52, with no difference between the groups (p = 0.114). Colectomy was performed in 23 patients (5.99%). Age, non-prior exposure to biological therapy, use of IFX and endoscopic remission at week 26 were associated with clinical remission after 52 weeks. Variables associated with endoscopic remission were non-prior exposure to biological therapy, and clinical and endoscopic remission at week 26. Conclusions: IFX was associated with higher rates of clinical remission after 1 year in comparison to ADA. Non-prior exposure to biological therapy and early response to anti-TNF treatment were associated with higher rates of clinical and endoscopic remission.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-01
2023-03-01T20:46:43Z
2023-03-01T20:46:43Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/s12876-022-02341-7
BMC Gastroenterology, v. 22, n. 1, 2022.
1471-230X
http://hdl.handle.net/11449/241093
10.1186/s12876-022-02341-7
2-s2.0-85131220737
url http://dx.doi.org/10.1186/s12876-022-02341-7
http://hdl.handle.net/11449/241093
identifier_str_mv BMC Gastroenterology, v. 22, n. 1, 2022.
1471-230X
10.1186/s12876-022-02341-7
2-s2.0-85131220737
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Gastroenterology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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