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

被引:0
作者
Protopapa, Maria [1 ]
Schmaul, Samantha [1 ]
Schraad, Muriel [1 ]
Pape, Katrin [1 ]
Zipp, Frauke [1 ]
Bittner, Stefan [2 ]
Uphaus, Timo [2 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Neurol, Focus Program Translat Neurosci FTN & Immunotherap, Rhine-Main Neurosci Network rmn2,Univ Med Ctr, Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Neurol, Focus Program Translat Neurosci,Rhine Main Neurosc, Langenbeckstr 1, D-55131 Mainz, Germany
关键词
interferon; leukopenia; multiple sclerosis; neutropenia; risk factors; safety; EXPRESSION; NEUTROPHILS;
D O I
10.1177/17562864241286497
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Interferon-beta (IFN-beta) 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: Our retrospective study compares laboratory findings and adverse events between subcutaneous (sc.) PEG-IFN-beta-1a and IFN-beta-1a in RRMS and CIS patients. Design: 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-beta-1a or sc. IFN-beta-1a (n = 202) were screened for eligibility. Patients who underwent regular laboratory controls in-house were included in our analysis (n = 128). Methods: 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/<mu>l) were assessed. Telephone interviews evaluated the side effects of the respective medication. A subgroup of patients was analyzed regarding neutrophil quantities and qualities. Results: Patients treated with sc. PEG-IFN-beta-1a had significantly lower leukocyte counts (p = 0.046) and higher incidences of leukopenia (p = 0.006) and neutropenia (p = 0.03) compared to sc. IFN-beta-1a. Clinical and MRI disease activity showed no significant differences, but people treated with sc. PEG-IFN-beta-1a reported more common adverse events such as joint/muscle pain, injection-site reaction, and infections. No serious adverse events were reported. Conclusion: Treatment with sc. PEG-IFN-beta-1a compared to unpegylated sc. IFN-beta 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.
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