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Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance

BACKGROUND: There is a need for postmarketing evidence generation for novel biologics and biosimilars. OBJECTIVE: To assess the feasibility, strengths, and limitations of the Biologics and Biosimilars Collective Intelligence Consortium (BBCIC) Distributed Research Network (DRN) to examine the utiliz...

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Autores principales: Zhang, Jie, Sridhar, Gayathri, Barr, Charles E., Eichelberger, Bernadette, Lockhart, Catherine M., Marshall, James, Clewell, Jerry, Accortt, Neil A., Curtis, Jeffrey R., Holmes, Cynthia, McMahill-Walraven, Cheryl N., Brown, Jeffrey S., Haynes, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Managed Care Pharmacy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391097/
https://www.ncbi.nlm.nih.gov/pubmed/32223608
http://dx.doi.org/10.18553/jmcp.2020.26.4.417
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author Zhang, Jie
Sridhar, Gayathri
Barr, Charles E.
Eichelberger, Bernadette
Lockhart, Catherine M.
Marshall, James
Clewell, Jerry
Accortt, Neil A.
Curtis, Jeffrey R.
Holmes, Cynthia
McMahill-Walraven, Cheryl N.
Brown, Jeffrey S.
Haynes, Kevin
author_facet Zhang, Jie
Sridhar, Gayathri
Barr, Charles E.
Eichelberger, Bernadette
Lockhart, Catherine M.
Marshall, James
Clewell, Jerry
Accortt, Neil A.
Curtis, Jeffrey R.
Holmes, Cynthia
McMahill-Walraven, Cheryl N.
Brown, Jeffrey S.
Haynes, Kevin
author_sort Zhang, Jie
collection PubMed
description BACKGROUND: There is a need for postmarketing evidence generation for novel biologics and biosimilars. OBJECTIVE: To assess the feasibility, strengths, and limitations of the Biologics and Biosimilars Collective Intelligence Consortium (BBCIC) Distributed Research Network (DRN) to examine the utilization and comparative safety of immune-modulating agents among patients with autoimmune diseases. METHODS: We conducted a retrospective cohort study among patients enrolled in health insurance plans participating in the BBCIC DRN between January 1, 2006, and September 30, 2015. Eligible patients were adult (≥18 years) new users of a disease-modifying nonbiologic and/or biologic agent with a prior diagnosis of rheumatoid arthritis (RA), other inflammatory conditions (psoriasis, psoriatic arthritis, ankylosing spondylitis), or inflammatory bowel disease (IBD). Follow-up started at treatment initiation and ended at the earliest of outcome occurrence (serious infection); treatment discontinuation; or switching, death, disenrollment, or end of study period. The study leveraged the FDA Sentinel System infrastructure for data management and analysis; descriptive statistics of patient characteristics and unadjusted incidence rates of study outcomes during follow-up were calculated. RESULTS: Eligible patient drug episodes included 111,611 with RA (75% female), 61,050 with other inflammatory conditions (51% female), and 30,628 with IBD (52% female). Across all 3 cohorts, approximately half of the patient drug episodes initiated a biologic (50% in RA; 60% in psoriasis, psoriatic arthritis, ankylosing spondylitis; and 55% in IBD). The crude incidence rate of serious infection was 9.8 (9.5-10.0) cases per 100 person-years in RA, 7.1 (6.8-7.5) in other inflammatory conditions, and 14.2 (13.6-14.8) in IBD patients. CONCLUSIONS: This study successfully identified large numbers of new users of biologics and produced results that were consistent with those from earlier published studies. The BBCIC DRN is a potential resource for surveillance of biologics.
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spelling pubmed-103910972023-08-02 Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance Zhang, Jie Sridhar, Gayathri Barr, Charles E. Eichelberger, Bernadette Lockhart, Catherine M. Marshall, James Clewell, Jerry Accortt, Neil A. Curtis, Jeffrey R. Holmes, Cynthia McMahill-Walraven, Cheryl N. Brown, Jeffrey S. Haynes, Kevin J Manag Care Spec Pharm Research BACKGROUND: There is a need for postmarketing evidence generation for novel biologics and biosimilars. OBJECTIVE: To assess the feasibility, strengths, and limitations of the Biologics and Biosimilars Collective Intelligence Consortium (BBCIC) Distributed Research Network (DRN) to examine the utilization and comparative safety of immune-modulating agents among patients with autoimmune diseases. METHODS: We conducted a retrospective cohort study among patients enrolled in health insurance plans participating in the BBCIC DRN between January 1, 2006, and September 30, 2015. Eligible patients were adult (≥18 years) new users of a disease-modifying nonbiologic and/or biologic agent with a prior diagnosis of rheumatoid arthritis (RA), other inflammatory conditions (psoriasis, psoriatic arthritis, ankylosing spondylitis), or inflammatory bowel disease (IBD). Follow-up started at treatment initiation and ended at the earliest of outcome occurrence (serious infection); treatment discontinuation; or switching, death, disenrollment, or end of study period. The study leveraged the FDA Sentinel System infrastructure for data management and analysis; descriptive statistics of patient characteristics and unadjusted incidence rates of study outcomes during follow-up were calculated. RESULTS: Eligible patient drug episodes included 111,611 with RA (75% female), 61,050 with other inflammatory conditions (51% female), and 30,628 with IBD (52% female). Across all 3 cohorts, approximately half of the patient drug episodes initiated a biologic (50% in RA; 60% in psoriasis, psoriatic arthritis, ankylosing spondylitis; and 55% in IBD). The crude incidence rate of serious infection was 9.8 (9.5-10.0) cases per 100 person-years in RA, 7.1 (6.8-7.5) in other inflammatory conditions, and 14.2 (13.6-14.8) in IBD patients. CONCLUSIONS: This study successfully identified large numbers of new users of biologics and produced results that were consistent with those from earlier published studies. The BBCIC DRN is a potential resource for surveillance of biologics. Academy of Managed Care Pharmacy 2020-04 /pmc/articles/PMC10391097/ /pubmed/32223608 http://dx.doi.org/10.18553/jmcp.2020.26.4.417 Text en Copyright © 2020, Academy of Managed Care Pharmacy. All rights reserved. https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research
Zhang, Jie
Sridhar, Gayathri
Barr, Charles E.
Eichelberger, Bernadette
Lockhart, Catherine M.
Marshall, James
Clewell, Jerry
Accortt, Neil A.
Curtis, Jeffrey R.
Holmes, Cynthia
McMahill-Walraven, Cheryl N.
Brown, Jeffrey S.
Haynes, Kevin
Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance
title Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance
title_full Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance
title_fullStr Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance
title_full_unstemmed Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance
title_short Incidence of Serious Infections and Design of Utilization and Safety Studies for Biologic and Biosimilar Surveillance
title_sort incidence of serious infections and design of utilization and safety studies for biologic and biosimilar surveillance
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391097/
https://www.ncbi.nlm.nih.gov/pubmed/32223608
http://dx.doi.org/10.18553/jmcp.2020.26.4.417
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