Lower leukocytes pretreatment as a possible risk factor for therapy-induced leukopenia in interferon-beta-treated patients with multiple sclerosis.

interferon leukopenia multiple sclerosis neutropenia risk factors safety

Journal

Therapeutic advances in neurological disorders
ISSN: 1756-2856
Titre abrégé: Ther Adv Neurol Disord
Pays: England
ID NLM: 101480242

Informations de publication

Date de publication:
2024
Historique:
received: 10 01 2024
accepted: 06 09 2024
medline: 31 10 2024
pubmed: 31 10 2024
entrez: 31 10 2024
Statut: epublish

Résumé

Interferon-beta (IFN-β) still plays a fundamental role in immunomodulation of people with multiple sclerosis (MS) with low disease activity and in clinically isolated syndrome (CIS). In 2014, pegylated (PEG) interferon was licensed by the European Medicines Agency (EMA) for relapsing-remitting MS (RRMS), enabling a lower dosing frequency. Our retrospective study compares laboratory findings and adverse events between subcutaneous (sc.) PEG-IFN-β-1a and IFN-β-1a in RRMS and CIS patients. Patients with CIS or RRMS fulfilling the revised McDonald criteria from 2017 visiting the neurology department of the University Medical Center of the Johannes Gutenberg University Mainz from 2010 to 2019 and treated with sc. PEG-IFN-β-1a or sc. IFN-β-1a ( We evaluate disease progression through clinical examination, relapse history, and magnetic resonance imaging (MRI) disease activity (gadolinium-enhancing or new T2 lesions). Relevant laboratory findings such as leukopenia (leukocyte count < 3.5/nl) and neutropenia (neutrophil count <43% of lymphocytes or <1500/µl) were assessed. Telephone interviews evaluated the side effects of the respective medication. A subgroup of patients was analyzed regarding neutrophil quantities and qualities. Patients treated with sc. PEG-IFN-β-1a had significantly lower leukocyte counts ( Treatment with sc. PEG-IFN-β-1a compared to unpegylated sc. IFN-β resulted in a significantly greater reduction in leukocyte and neutrophil levels with a higher incidence of side effects. We suggest mandatory monitoring of differential blood counts before and during treatment. Possible risk factors for the occurrence of leukopenia in patients with multiple sclerosis treated with interferon beta In our study, we compared two medications used to treat multiple sclerosis (MS): pegylated interferon-beta-1a (PEG-IFN-beta-1a) and interferon-beta-1a (IFN-beta-1a). The pegylated form needs to be taken less often. We looked at patients’ medical history, physical exams, lab results, and MRI scans to see how these drugs affected them. We also asked about side effects during phone interviews. We found that PEG-IFN-beta-1a caused lower levels of certain blood cells, like leukocytes, and more side effects such as skin rashes and infections compared to IFN-beta-1a. However, there were no differences in disease activity as seen in clinical exams and MRI scans. We recommend regular blood tests for patients using these medications to monitor their health.

Sections du résumé

Background UNASSIGNED
Interferon-beta (IFN-β) still plays a fundamental role in immunomodulation of people with multiple sclerosis (MS) with low disease activity and in clinically isolated syndrome (CIS). In 2014, pegylated (PEG) interferon was licensed by the European Medicines Agency (EMA) for relapsing-remitting MS (RRMS), enabling a lower dosing frequency.
Objectives UNASSIGNED
Our retrospective study compares laboratory findings and adverse events between subcutaneous (sc.) PEG-IFN-β-1a and IFN-β-1a in RRMS and CIS patients.
Design UNASSIGNED
Patients with CIS or RRMS fulfilling the revised McDonald criteria from 2017 visiting the neurology department of the University Medical Center of the Johannes Gutenberg University Mainz from 2010 to 2019 and treated with sc. PEG-IFN-β-1a or sc. IFN-β-1a (
Methods UNASSIGNED
We evaluate disease progression through clinical examination, relapse history, and magnetic resonance imaging (MRI) disease activity (gadolinium-enhancing or new T2 lesions). Relevant laboratory findings such as leukopenia (leukocyte count < 3.5/nl) and neutropenia (neutrophil count <43% of lymphocytes or <1500/µl) were assessed. Telephone interviews evaluated the side effects of the respective medication. A subgroup of patients was analyzed regarding neutrophil quantities and qualities.
Results UNASSIGNED
Patients treated with sc. PEG-IFN-β-1a had significantly lower leukocyte counts (
Conclusion UNASSIGNED
Treatment with sc. PEG-IFN-β-1a compared to unpegylated sc. IFN-β resulted in a significantly greater reduction in leukocyte and neutrophil levels with a higher incidence of side effects. We suggest mandatory monitoring of differential blood counts before and during treatment.
Possible risk factors for the occurrence of leukopenia in patients with multiple sclerosis treated with interferon beta In our study, we compared two medications used to treat multiple sclerosis (MS): pegylated interferon-beta-1a (PEG-IFN-beta-1a) and interferon-beta-1a (IFN-beta-1a). The pegylated form needs to be taken less often. We looked at patients’ medical history, physical exams, lab results, and MRI scans to see how these drugs affected them. We also asked about side effects during phone interviews. We found that PEG-IFN-beta-1a caused lower levels of certain blood cells, like leukocytes, and more side effects such as skin rashes and infections compared to IFN-beta-1a. However, there were no differences in disease activity as seen in clinical exams and MRI scans. We recommend regular blood tests for patients using these medications to monitor their health.

Autres résumés

Type: plain-language-summary (eng)
Possible risk factors for the occurrence of leukopenia in patients with multiple sclerosis treated with interferon beta In our study, we compared two medications used to treat multiple sclerosis (MS): pegylated interferon-beta-1a (PEG-IFN-beta-1a) and interferon-beta-1a (IFN-beta-1a). The pegylated form needs to be taken less often. We looked at patients’ medical history, physical exams, lab results, and MRI scans to see how these drugs affected them. We also asked about side effects during phone interviews. We found that PEG-IFN-beta-1a caused lower levels of certain blood cells, like leukocytes, and more side effects such as skin rashes and infections compared to IFN-beta-1a. However, there were no differences in disease activity as seen in clinical exams and MRI scans. We recommend regular blood tests for patients using these medications to monitor their health.

Identifiants

pubmed: 39479177
doi: 10.1177/17562864241286497
pii: 10.1177_17562864241286497
pmc: PMC11523160
doi:

Types de publication

Journal Article

Langues

eng

Pagination

17562864241286497

Informations de copyright

© The Author(s), 2024.

Auteurs

Maria Protopapa (M)

Department of Neurology, Focus Program Translational Neuroscience, (FTN), and Immunotherapy (FZI), Rhine-Main Neuroscience Network (rmn2), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Samantha Schmaul (S)

Department of Neurology, Focus Program Translational Neuroscience, (FTN), and Immunotherapy (FZI), Rhine-Main Neuroscience Network (rmn2), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Muriel Schraad (M)

Department of Neurology, Focus Program Translational Neuroscience, (FTN), and Immunotherapy (FZI), Rhine-Main Neuroscience Network (rmn2), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Katrin Pape (K)

Department of Neurology, Focus Program Translational Neuroscience, (FTN), and Immunotherapy (FZI), Rhine-Main Neuroscience Network (rmn2), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Frauke Zipp (F)

Department of Neurology, Focus Program Translational Neuroscience, (FTN), and Immunotherapy (FZI), Rhine-Main Neuroscience Network (rmn2), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Stefan Bittner (S)

Department of Neurology, Focus Program Translational Neuroscience, Rhine-Main Neuroscience Network, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstrasse 1, Mainz 55131, Germany.

Timo Uphaus (T)

Department of Neurology, Focus Program Translational Neuroscience, Rhine-Main Neuroscience Network, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstrasse 1, Mainz 55131, Germany.

Classifications MeSH