Changes in selected haematological parameters associated with JAK1/JAK2 inhibition observed in patients with rheumatoid arthritis treated with baricitinib.


Journal

RMD open
ISSN: 2056-5933
Titre abrégé: RMD Open
Pays: England
ID NLM: 101662038

Informations de publication

Date de publication:
10 2020
Historique:
received: 18 06 2020
revised: 28 08 2020
accepted: 22 09 2020
entrez: 8 10 2020
pubmed: 9 10 2020
medline: 1 9 2021
Statut: ppublish

Résumé

To characterise changes in selected haematological parameters following once-daily oral baricitinib dosing. Data were pooled from eight randomised clinical trials (four phase 3, three phase 2, one phase 1b) and one long-term extension. Changes in haematological parameters were evaluated up to 128 weeks (N=2387); overall safety of baricitinib was assessed up to 6 years (N=3492). Mean absolute neutrophil counts decreased (-1.36×10 Moderate decreases in neutrophils were seen during baricitinib treatment; however, serious infection was uncommon in patients with neutropenia. Transient increases were observed in lymphocytes and platelets, which returned to baseline over time. Changes in haemoglobin concentration were generally small. Haematological abnormalities seldom led to drug discontinuation.

Identifiants

pubmed: 33028675
pii: rmdopen-2020-001370
doi: 10.1136/rmdopen-2020-001370
pmc: PMC7722368
pii:
doi:

Substances chimiques

Antirheumatic Agents 0
Azetidines 0
Purines 0
Pyrazoles 0
Sulfonamides 0
JAK1 protein, human EC 2.7.10.2
JAK2 protein, human EC 2.7.10.2
Janus Kinase 1 EC 2.7.10.2
Janus Kinase 2 EC 2.7.10.2
baricitinib ISP4442I3Y

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: JK reports grants paid to the University of Massachusetts Medical School from AbbVie, Genentech, Gilead Sciences, Pfizer and UCB; and personal fees from AbbVie, Amgen, Alvotech Suisse AG, Arena Pharmaceuticals, Boehringer Ingelheim GmbH, Celltrion Healthcare Co., Janssen Biotech, Merck Sharp & Dohme Corp., Mylan, Novartis AG, Pfizer, Samsung Bioepis, Sandoz and UCB. MH reports grants and personal fees from Bristol-Myers Squibb K.K. and AbbVie Japan; grants from Eisai, Ayumi Pharmaceutical Co., Nippon Kayaku Co., Mitsubishi Tanabe Pharma Co., and Teijin Pharma; and personal fees from Eli Lilly and Company, Boehringer-ingelheim, Kissei Pharmaceutical Co., and Chugai Pharmaceutical Co.. JR, CD, MI, IdlT, YI, AC and CS were employees and shareholders of Eli Lilly and Company. TM was an employee of Syneos Health under contract to Eli Lilly and Company. EK reports grants and personal fees from AbbVie, Amgen, Gilead, Merck, Eli Lilly and Company, Pfizer; grants from PuraPharm; and personal fees from AstraZeneca Pharma, Bristol-Myers Squibb, Celltrion, Jannsen, Myriad Autoimmune, F. Hoffmann-La Roche & Co, Genentech, Sandoz, Sanofi Genzyme, Samsung Bioepsis, and UCB. RFvV reports research support and Grants from Bristol-Myers Squibb, GSK, Eli Lilly and Co., Pfizer, UCB Pharma. Consultancy, honoraria: AbbVie, AstraZeneca, Biotest, Celgene, GlaxoSmithKline, Janssen, Eli Lilly and Co., Novartis, Pfizer, Servier, UCB. JTG reports personal fees from AbbVie, Bristol-Myers Squibb, Eli Lilly and Co., and UCB, and grants from Pfizer. TWJH from the Department of Rheumatology LUMC has received research support/lecture fees/consultancy fees from Abblynx, Merck, UCB, Bristol-Myers Squibb, Biotest AG, Janssen, Pfzer, Novartis, Roche, Sanofi-Aventis, Abbott, Crescendo Bioscience, Galapagos, Nycomed, Boeringher, Takeda, Zydus, Epirus and Eli Lilly and Co. JMK is a consultant and shareholder of Corrona, LLC, and a consultant for AbbVie, Amgen, Bristol-Myers Squibb, Genentech, Gilead, GlaxoSmithKline, Eli Lilly and Co., Pfizer, Regeneron and Sanofi.

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Auteurs

Jonathan Kay (J)

Division of Rheumatology, Department of Medicine, UMass Memorial Medical Center, Worcester, Massachusetts, USA jonathan.kay@umassmemorial.org.
Division of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Department of Population and Quantitative Health Sciences, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

Masayoshi Harigai (M)

Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan.

Josh Rancourt (J)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Christina Dickson (C)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Thomas Melby (T)

Syneos Health, Morrisville, North Carolina, USA.

Maher Issa (M)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Inmaculada de la Torre (I)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Yoshitaka Isaka (Y)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Anabela Cardoso (A)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Chadi Saifan (C)

Eli Lilly and Company, Indianapolis, Indiana, USA.

Edward C Keystone (EC)

Rebecca MacDonald Centre for Arthritis and Autoimmune Disease, Mount Sinai Hospital, Toronto, Ontario, Canada.

Ronald F van Vollenhoven (RF)

Department of Rheumatology and Clinical Immunology, Amsterdam Universitair Medische Centra, Amsterdam, The Netherlands.

Jon T Giles (JT)

Division of Rheumatology, Department of Medicine, Columbia University College of Physicians and Surgeons, New York City, New York, USA.

Tom Wj Huizinga (TW)

Department of Rheumatology, Leids Universitair Medisch Centrum, Leiden, The Netherlands.

Joel M Kremer (JM)

Division of Rheumatology, Department of Medicine, Albany Medical College, Albany, New York, USA.

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Classifications MeSH