Incidence and associated risk factors for invasive fungal infections and other serious infections in patients on ibrutinib.


Journal

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
ISSN: 1437-7780
Titre abrégé: J Infect Chemother
Pays: Netherlands
ID NLM: 9608375

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 12 04 2021
revised: 29 07 2021
accepted: 05 08 2021
pubmed: 15 8 2021
medline: 28 10 2021
entrez: 14 8 2021
Statut: ppublish

Résumé

Ibrutinib is a small molecule tyrosine kinase inhibitor that blocks the activity of B cells and other immune effectors and is used in a variety of hematologic malignancies. There have been numerous reports of increased frequency of serious infections including invasive fungal infections (IFI) in patients on ibrutinib. Demographic and clinical features of all patients receiving ibrutinib at a single tertiary care center were collected from electronic medical records. Univariate and multivariate statistical analyses were performed to find out the factors associated with infection. A total of 244 patients received ibrutinib for hematologic malignancies, of which 44 (18.0%) experienced ≥ 1 serious infection including 5 (2.0%) with IFI (1 pulmonary cryptococcosis, 4 pulmonary aspergillosis), 39 (16.0%) with bacterial infections and 8 (3.3%) with viral infections. Ten patients (4.1%) experienced multiple infections or co-infections while on ibrutinib and 10 (4.1%) expired or were transferred to hospice as a result of infection. In multivariate analysis risk factors that were less common in uninfected versus infected patients included advanced age (73 years vs. 77 years), Eastern Cooperative Oncologic Grade (ECOG) performance score ≥ 2 (6.5% vs. 31.8%) and concurrent use of steroids (4.5% vs. 20.5%) or other cytotoxic agents (0% vs. 4.6%). There was a high rate of serious infection but relatively few IFI in patients receiving ibrutinib. Most patients who developed serious infections while on ibrutinib had additional predisposing risk factors including concurrent use of steroids or other cytotoxic agents, advanced age and frailty.

Sections du résumé

BACKGROUND BACKGROUND
Ibrutinib is a small molecule tyrosine kinase inhibitor that blocks the activity of B cells and other immune effectors and is used in a variety of hematologic malignancies. There have been numerous reports of increased frequency of serious infections including invasive fungal infections (IFI) in patients on ibrutinib.
METHODS METHODS
Demographic and clinical features of all patients receiving ibrutinib at a single tertiary care center were collected from electronic medical records. Univariate and multivariate statistical analyses were performed to find out the factors associated with infection.
RESULTS RESULTS
A total of 244 patients received ibrutinib for hematologic malignancies, of which 44 (18.0%) experienced ≥ 1 serious infection including 5 (2.0%) with IFI (1 pulmonary cryptococcosis, 4 pulmonary aspergillosis), 39 (16.0%) with bacterial infections and 8 (3.3%) with viral infections. Ten patients (4.1%) experienced multiple infections or co-infections while on ibrutinib and 10 (4.1%) expired or were transferred to hospice as a result of infection. In multivariate analysis risk factors that were less common in uninfected versus infected patients included advanced age (73 years vs. 77 years), Eastern Cooperative Oncologic Grade (ECOG) performance score ≥ 2 (6.5% vs. 31.8%) and concurrent use of steroids (4.5% vs. 20.5%) or other cytotoxic agents (0% vs. 4.6%).
CONCLUSIONS CONCLUSIONS
There was a high rate of serious infection but relatively few IFI in patients receiving ibrutinib. Most patients who developed serious infections while on ibrutinib had additional predisposing risk factors including concurrent use of steroids or other cytotoxic agents, advanced age and frailty.

Identifiants

pubmed: 34389223
pii: S1341-321X(21)00217-8
doi: 10.1016/j.jiac.2021.08.005
pii:
doi:

Substances chimiques

Piperidines 0
ibrutinib 1X70OSD4VX
Adenine JAC85A2161

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1700-1705

Informations de copyright

Copyright © 2021 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

Thomas Holowka (T)

Department of Internal Medicine, Yale School of Medicine, 333 Cedar St, New Haven, CT, 06510, USA. Electronic address: thomas.holowka@unchealth.unc.edu.

Harry Cheung (H)

Yale School of Medicine, 367 Cedar St, New Haven, CT, 06510, USA. Electronic address: harry.cheung@yale.edu.

Maricar Malinis (M)

Section of Infectious Disease, Department of Internal Medicine, Yale School of Medicine, USA. Electronic address: maricar.malinis@yale.edu.

Geliang Gan (G)

Yale Center for Analytical Science, Yale School of Public Health, PO Box 208034, New Haven, CT, 06520, USA. Electronic address: geliang.gan@yale.edu.

Yanhong Deng (Y)

Yale Center for Analytical Science, Yale School of Public Health, PO Box 208034, New Haven, CT, 06520, USA. Electronic address: yanhong.deng@yale.edu.

Sarah Perreault (S)

Department of Pharmacy, Yale New Haven Health, 20 York St, New Haven, CT, 06510, USA. Electronic address: sarah.perreault@ynhh.org.

Iris Isufi (I)

Section of Hematology, Department of Internal Medicine, Yale School of Medicine, 333 Cedar St, New Haven, CT, 06510, USA. Electronic address: iris.isufi@yale.edu.

Marwan M Azar (MM)

Section of Infectious Disease, Department of Internal Medicine, Yale School of Medicine, 333 Cedar St, New Haven, CT, 06510, USA. Electronic address: marwan.azar@yale.edu.

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Classifications MeSH