Infections in patients with mantle cell lymphoma.


Journal

HemaSphere
ISSN: 2572-9241
Titre abrégé: Hemasphere
Pays: United States
ID NLM: 101740619

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 23 01 2024
revised: 26 04 2024
accepted: 21 05 2024
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 9 7 2024
Statut: epublish

Résumé

Advancements in treatments have significantly improved the prognosis for mantle cell lymphoma (MCL), and there is a growing population of survivors with an increased susceptibility to infections. We assessed the incidence of infections by clinical characteristics and treatment both before and after MCL diagnosis in Sweden. Patients with a diagnosis of MCL ≥ 18 years between 2007 and 2019 were included, along with up to 10 matched comparators. Infectious disease diagnosis and anti-infective drug dispensation were identified by the National Patient and the Prescribed Drug Registers, respectively. Patients and comparators were followed from the diagnosis/matching date until death, emigration, or June 30, 2020. Overall, 1559 patients and 15,571 comparators were followed for a median duration of 2.9 and 5 years, respectively. The infection rate among patients was twofold higher, RRadj = 2.14 (2.01-2.27), contrasted to the comparator group. There was a notable rise in infection rates already 4 years before MCL diagnosis, which reached a fourfold increase in the first year after diagnosis and persisted significantly increased for an additional 8 years. Among patients, 69% (

Identifiants

pubmed: 38978637
doi: 10.1002/hem3.121
pii: HEM3121
pmc: PMC11228544
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e121

Informations de copyright

© 2024 The Author(s). HemaSphere published by John Wiley & Sons Ltd on behalf of European Hematology Association.

Déclaration de conflit d'intérêts

Mats Jerkeman received honoraria from Abbvie, AstraZeneca, BMS, Kite/Gilead, Pierre Fabre, Roche, Sobi, and Takeda and research support from Abbvie, AstraZeneca, BMS, and Roche. Ingrid Glimelius received research support from Takeda and participated in educational sessions arranged by Janssen Cilag, Abbvie, and Kite Gilead. Karin E. Smedby received honoraria from Incyte and Celgene, and research support from Janssen Cilag. The other authors have no relevant financial or nonfinancial interests to disclose.

Auteurs

Kossi D Abalo (KD)

Department of Immunology, Genetics and Pathology, Cancer Precision Medicine Uppsala University Uppsala Sweden.
Department of Medicine Solna, Clinical Epidemiology Division Karolinska Institutet Stockholm Sweden.

Sara Ekberg (S)

Department of Immunology, Genetics and Pathology, Cancer Precision Medicine Uppsala University Uppsala Sweden.
Department of Medicine Solna, Clinical Epidemiology Division Karolinska Institutet Stockholm Sweden.

Therese M L Andersson (TML)

Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden.

Simon Pahnke (S)

Department of Immunology, Genetics and Pathology, Cancer Precision Medicine Uppsala University Uppsala Sweden.

Alexandra Albertsson-Lindblad (A)

Division of Oncology, Department of Clinical Sciences Lund, Skåne University Hospital Lund University Lund Sweden.

Karin E Smedby (KE)

Department of Medicine Solna, Clinical Epidemiology Division Karolinska Institutet Stockholm Sweden.
Department of Hematology Karolinska University Hospital Stockholm Sweden.

Mats Jerkeman (M)

Division of Oncology, Department of Clinical Sciences Lund, Skåne University Hospital Lund University Lund Sweden.

Ingrid Glimelius (I)

Department of Immunology, Genetics and Pathology, Cancer Precision Medicine Uppsala University Uppsala Sweden.
Department of Medicine Solna, Clinical Epidemiology Division Karolinska Institutet Stockholm Sweden.

Classifications MeSH