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DOI 10.1016/j.msard.2023.105048

Медицинская библиотека · Multiple sclerosis and related disorders · 2023

Lessons learned after 20 years of real-world experience with natalizumab.

Khatri Bhupendra O, Olapo Tayo, Beals Sara, Lindman Emily, Perea Toni, Van Zealand Pamela, Metzger Ryan R

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Аннотация

BACKGROUND

While natalizumab (NTZ) is an effective therapy for multiple sclerosis (MS), it is associated with an increased risk of progressive multifocal leukoencephalopathy (PML). After 20 years (2002-2022) of experience with NTZ at our center, we observed no cases of PML.

OBJECTIVES

We evaluated the likelihood of experiencing PML in a subset of our treatment cohort, as well as reviewed treatment practices at our center that may mitigate PML risk.

METHODS

For this retrospective study, we reviewed patient characteristics, treatment practices, and clinical and MRI findings in patients receiving NTZ from 2006 to 2020. Observation of no PML cases was compared to the global and US PML incidences, and to the expected incidence based on published risk estimates.

RESULTS

766 patients were evaluated. The number of NTZ infusions received ranged from 1 to 126, with a mean of 28. Patients received neurological examination prior to each infusion, which sometimes resulted in a pause in therapy to rule out PML if clinical worsening occurred. Extended interval dosing (EID) was the overall dosing schedule for 31% of patients. EID did not result in higher rates of radiological disease worsening than standard interval dosing (SID) patients. Depending on the analysis conducted, the finding of 0 PML cases in our cohort ranged from slightly unexpected to slightly expected.

CONCLUSIONS

The utilization of EID as well as regular clinical monitoring of patients may have lowered PML risk while still maintaining NTZ efficacy.

Для цитирования: Khatri Bhupendra O, Olapo Tayo, Beals Sara, Lindman Emily, Perea Toni, Van Zealand Pamela, Metzger Ryan R. Lessons learned after 20 years of real-world experience with natalizumab.. Multiple sclerosis and related disorders. 2023. DOI: 10.1016/j.msard.2023.105048.

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