Literature DB >> 31016578

Changing rate of serious infections in biologic-exposed rheumatoid arthritis patients. Data from South American registries BIOBADABRASIL and BIOBADASAR.

Roberto Ranza1,2, Maria Celina de la Vega3, Ieda Maria Magalhães Laurindo4, Marìa Gimena Gómez5, David Cezar Titton6, Adriana Maria Kakehasi7, Alejandro Brigante5, Alejandro Benitez3, Aline Ranzolin8, Amelia Granel9, Ana María Cappuccio10, Ana Quinteros11, André Luiz Shinji Hayata12, Andrea Smichowski13, Ângela Luzia Branco P Duarte14, Barbara Stadler Kahlow15, Carolina Sánchez Andia16, Claiton Viegas Brenol17, Edson Velozo18, Eduardo Mussano19, Enrique R Soriano20, Georges Basile Christopoulos21, Geraldo da Rocha Castelar Pinheiro22, Gláucio Ricardo Werner de Castro23, Gustavo Casado13, Hellen Mary da Silveira Carvalho24, Ida Elena Exeni25, Inês Guimarães da Silveira26, Ingrid Petkovic27, Ivanio Alves Pereira28, Izaias Pereira da Costa29, Javier Eduardo Rosa22, José Roberto Silva Miranda30, Julio Cesar Bertacini de Moraes31, Manoel Barros Bertolo32, Manuel Buhl33, Maria Alícia Lázaro34, Maria de Fátima Lobato C da Sauma35, Marcelo de Medeiros Pinheiro36, Monica Díaz37, Mônica Valéria Siqueira Santana de Vechi38, Osvaldo Luis Cerda39, Pablo Astesana40, Pablo Finucci Curi41, Paulo Louzada-Jr42, Reginaldo Botelho Teodoro43, Roberto Acayaba Toledo44, Sílvia Papasidero45, Valeria Valim46, Vander Fernandes47, Veronica Saurit48, Washington Alves Bianchi49, Rogério de Melo Costa Pinto50, Miguel Angel Descalzo51, Juan Jesus Gomez-Reino52.   

Abstract

OBJECTIVE: Most reports on serious infections (SI) in rheumatoid arthritis (RA) patients treated with biological disease-modifying antirheumatic drugs (bDMARDs) are from the USA and Western Europe. Data from other regions are largely missing. We report data from South American countries with different backgrounds and health-care systems but similar registries.
METHODS: We merged 2010-2016 data from two registries, BIOBADABRASIL (Brazil) and BIOBADASAR (Argentina), which share the same protocol, online platform and data monitoring process. Patients with active RA were included when they began the first bDMARD or a conventional synthetic DMARD (csDMARD, control group). The SI incidence rate (IR) per 1000 patient/years and adjusted IR ratio (aIRR) were estimated for bDMARDs and csDMARDs.
RESULTS: Data were analysed for 3717 RA patients with an exposure of 13,380 patient/years. The 2591 patients treated with bDMARDs (64% tumour necrosis factor-α inhibitors (TNFi)) had a follow-up of 9300 years, and the 1126 treated with csDMARDs had an exposure of 4081 patient/years. The SI IR was 30.54 (CI 27.18-34.30) for all bDMARDs and 5.15 (CI 3.36-7.89) for csDMARDs. The aIRR between the two groups was 2.03 ([1.05, 3.9] p = 0.034) for the first 6 months of treatment but subsequently increased to 8.26 ([4.32, 15.76] p < 0.001). The SI IR for bDMARDs decreased over time in both registries, dropping from 36.59 (28.41-47.12) in 2012 to 7.27 (4.79-11.05) in 2016.
CONCLUSION: While SI remains a major concern in South American patients with RA treated with bDMARDs, a favourable trend toward a reduction was observed in the last years.Key Points• New comprehensive data on biologic drugs safety from international collaboration in South America.• First proposal for national registries data merging in South America.• Serious infections remain a major concern in RA patients treated with biologics.• A significant reduction of serious infections in RA patients exposed to biologics was observed over a 7 years period.

Entities:  

Keywords:  Biological agents; Registries; Rheumatoid arthritis; Safety; Serious infections

Mesh:

Substances:

Year:  2019        PMID: 31016578     DOI: 10.1007/s10067-019-04516-2

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  35 in total

1.  Infections in patients treated with tumor necrosis factor antagonists: incidence, etiology and mortality in the BIOBADASER registry.

Authors:  María José Pérez-Sola; Julián Torre-Cisneros; Beatriz Pérez-Zafrilla; Loreto Carmona; Miguel Angel Descalzo; Juan Jesús Gómez-Reino
Journal:  Med Clin (Barc)       Date:  2011-04-22       Impact factor: 1.725

2.  The risk of serious infection in patients with rheumatoid arthritis treated with tumor necrosis factor inhibitors decreased over time: a report from the registry of Japanese rheumatoid arthritis patients on biologics for long-term safety (REAL) database.

Authors:  Ryoko Sakai; Soo-Kyung Cho; Toshihiro Nanki; Ryuji Koike; Kaori Watanabe; Hayato Yamazaki; Hayato Nagasawa; Koichi Amano; Yoshiya Tanaka; Takayuki Sumida; Atsushi Ihata; Shinsuke Yasuda; Atsuo Nakajima; Takahiko Sugihara; Naoto Tamura; Takao Fujii; Hiroaki Dobashi; Yasushi Miura; Nobuyuki Miyasaka; Masayoshi Harigai
Journal:  Rheumatol Int       Date:  2014-05-23       Impact factor: 2.631

3.  BIOBADASER, BIOBADAMERICA, and BIOBADADERM: safety registers sharing commonalities across diseases and countries.

Authors:  L Carmona; M de la Vega; R Ranza; G Casado; D C Titton; M Á Descalzo; Juan Gómez-Reino
Journal:  Clin Exp Rheumatol       Date:  2014-10-30       Impact factor: 4.473

4.  A Study of Multiple Causes of Death in Rheumatoid Arthritis.

Authors:  Frederico A G Pinheiro; Deborah C C Souza; Emilia I Sato
Journal:  J Rheumatol       Date:  2015-10-15       Impact factor: 4.666

Review 5.  The Risk of Tuberculosis in Patients with Rheumatoid Arthritis Treated with Tumor Necrosis Factor-α Antagonist: A Metaanalysis of Both Randomized Controlled Trials and Registry/Cohort Studies.

Authors:  Jing-Wen Ai; Shu Zhang; Qiao-Ling Ruan; Yi-Qi Yu; Bing-Yan Zhang; Qi-Hui Liu; Wen-Hong Zhang
Journal:  J Rheumatol       Date:  2015-10-15       Impact factor: 4.666

Review 6.  Safety of synthetic and biological DMARDs: a systematic literature review informing the 2016 update of the EULAR recommendations for management of rheumatoid arthritis.

Authors:  Sofia Ramiro; Alexandre Sepriano; Katerina Chatzidionysiou; Jackie L Nam; Josef S Smolen; Désirée van der Heijde; Maxime Dougados; Ronald van Vollenhoven; Johannes W Bijlsma; Gerd R Burmester; Marieke Scholte-Voshaar; Louise Falzon; Robert B M Landewé
Journal:  Ann Rheum Dis       Date:  2017-03-15       Impact factor: 19.103

Review 7.  The safety of anti-tumour necrosis factor therapy in rheumatoid arthritis.

Authors:  Johan Askling; Will Dixon
Journal:  Curr Opin Rheumatol       Date:  2008-03       Impact factor: 5.006

8.  Predictors for the 5-year risk of serious infections in patients with rheumatoid arthritis treated with anti-tumour necrosis factor therapy: a cohort study in the Dutch Rheumatoid Arthritis Monitoring (DREAM) registry.

Authors:  Sanne A A van Dartel; Jaap Fransen; Wietske Kievit; Ellen A J Dutmer; Herman L M Brus; Nella M Houtman; Mart A F van de Laar; Piet L C M van Riel
Journal:  Rheumatology (Oxford)       Date:  2013-01-30       Impact factor: 7.580

Review 9.  Risk of herpes/herpes zoster during anti-tumor necrosis factor therapy in patients with rheumatoid arthritis. Systematic review and meta-analysis.

Authors:  Helene Che; Cedric Lukas; Jacques Morel; Bernard Combe
Journal:  Joint Bone Spine       Date:  2013-08-07       Impact factor: 4.929

10.  Treatment benefit or survival of the fittest: what drives the time-dependent decrease in serious infection rates under TNF inhibition and what does this imply for the individual patient?

Authors:  A Strangfeld; M Eveslage; M Schneider; H J Bergerhausen; T Klopsch; A Zink; J Listing
Journal:  Ann Rheum Dis       Date:  2011-07-25       Impact factor: 19.103

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  1 in total

1.  Adverse Events in Patients With Rheumatoid Arthritis and Psoriatic Arthritis Receiving Long-Term Biological Agents in a Real-Life Setting.

Authors:  Mayara Costa de Camargo; Bruna Cipriano Almeida Barros; Izabela Fulone; Marcus Tolentino Silva; Miriam Sanches do Nascimento Silveira; Iara Alves de Camargo; Silvio Barberato-Filho; Fernando de Sá Del Fiol; Luciane Cruz Lopes
Journal:  Front Pharmacol       Date:  2019-09-11       Impact factor: 5.810

  1 in total

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