Literature DB >> 26395500

Opportunistic infections and biologic therapies in immune-mediated inflammatory diseases: consensus recommendations for infection reporting during clinical trials and postmarketing surveillance.

K L Winthrop1, S A Novosad2, J W Baddley3, L Calabrese4, T Chiller5, P Polgreen6, F Bartalesi7, M Lipman8, X Mariette9, O Lortholary10, M E Weinblatt11, M Saag3, J Smolen12.   

Abstract

No consensus has previously been formed regarding the types and presentations of infectious pathogens to be considered as 'opportunistic infections' (OIs) within the setting of biologic therapy. We systematically reviewed published literature reporting OIs in the setting of biologic therapy for inflammatory diseases. The review sought to describe the OI definitions used within these studies and the types of OIs reported. These findings informed a consensus committee (infectious diseases and rheumatology specialists) in deliberations regarding the development of a candidate list of infections that should be considered as OIs in the setting of biologic therapy. We reviewed 368 clinical trials (randomised controlled/long-term extension), 195 observational studies and numerous case reports/series. Only 11 observational studies defined OIs within their methods; no consistent OI definition was identified across studies. Across all study formats, the most numerous OIs reported were granulomatous infections. The consensus group developed a working definition for OIs as 'indicator' infections, defined as specific pathogens or presentations of pathogens that 'indicate' the likelihood of an alteration in host immunity in the setting of biologic therapy. Using this framework, consensus was reached upon a list of OIs and case-definitions for their reporting during clinical trials and other studies. Prior studies of OIs in the setting of biologic therapy have used inconsistent definitions. The consensus committee reached agreement upon an OI definition, developed case definitions for reporting of each pathogen, and recommended these be used in future studies to facilitate comparison of infection risk between biologic therapies. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Entities:  

Keywords:  Anti-TNF; Infections; Rheumatoid Arthritis

Mesh:

Substances:

Year:  2015        PMID: 26395500     DOI: 10.1136/annrheumdis-2015-207841

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  38 in total

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Journal:  Intensive Care Med       Date:  2017-09-25       Impact factor: 17.440

3.  Long-term safety of single-agent ibrutinib in patients with chronic lymphocytic leukemia in 3 pivotal studies.

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4.  A risk score for predicting hospitalization for community-acquired pneumonia in ITP using nationally representative data.

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5.  Safety of Ixekizumab in Adult Patients with Moderate-to-Severe Psoriasis: Data from 17 Clinical Trials with Over 18,000 Patient-Years of Exposure.

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Review 7.  Acute exacerbation of interstitial lung disease associated with rheumatic disease.

Authors:  Fabrizio Luppi; Marco Sebastiani; Carlo Salvarani; Elisabeth Bendstrup; Andreina Manfredi
Journal:  Nat Rev Rheumatol       Date:  2021-12-07       Impact factor: 20.543

8.  Safety of ixekizumab in patients with psoriatic arthritis: data from four clinical trials with over 2000 patient-years of exposure.

Authors:  Atul A Deodhar; Bernard Combe; Ana P Accioly; Rebecca Bolce; Danting Zhu; Amanda M Gellett; Aubrey Trevelin Sprabery; Gerd-Rüdiger R Burmester
Journal:  Ann Rheum Dis       Date:  2022-04-07       Impact factor: 27.973

9.  Increasing incidence associated with herpes zoster infection in British Columbia, Canada.

Authors:  Fawziah Marra; Mei Chong; Mehdi Najafzadeh
Journal:  BMC Infect Dis       Date:  2016-10-20       Impact factor: 3.090

10.  Long-term safety of certolizumab pegol in plaque psoriasis: pooled analysis over 3 years from three phase III, randomized, placebo-controlled studies.

Authors:  A Blauvelt; C Paul; P van de Kerkhof; R B Warren; A B Gottlieb; R G Langley; F Brock; C Arendt; M Boehnlein; M Lebwohl; K Reich
Journal:  Br J Dermatol       Date:  2020-09-06       Impact factor: 9.302

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