期刊
NEUROLOGICAL SCIENCES
卷 42, 期 8, 页码 3297-3303出版社
SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10072-020-05022-z
关键词
Migraine; Erenumab; Prevention; Calcitonin-gene-related peptide
The study evaluated early outcomes of erenumab discontinuation in migraine patients who had a continuous positive response. Results showed that most patients experienced worsening symptoms in the first 4 weeks after treatment cessation, although still lower than baseline. More than half of the patients had an early disease worsening, while others maintained their responder status after treatment completion. Further studies are needed to identify predictors of prolonged response to erenumab and determine the optimal treatment duration based on patients' characteristics.
Background Monoclonal antibodies targeting the calcitonin gene-related peptide, including erenumab, are migraine-specific preventive treatments, whose long-term effectiveness has still to be evaluated in real-life settings. We assessed early outcomes of erenumab discontinuation after a 52-week treatment in patients with a continuous positive response to the drug. Methods We evaluated the early outcomes after treatment completion in migraineurs from a real-life multicenter register. All patients received monthly erenumab for 52 weeks and attended a 8-week follow-up after treatment completion. Primary outcomes were responder rates and changes in monthly migraine days (MMDs), acute medications days (AMDs), and pain intensity on a Numerical Rating Scale (NRS score) during weeks 1-4 after erenumab treatment completion. Results The 32 included patients reported a decrease in MMDs, AMDs, and NRS score during the last 4 weeks of treatment compared with baseline (P<0.001). During weeks 1-4 after treatment completion, all the outcome measures increased compared with the last 4 weeks of treatment (P < 0.001) despite staying lower than baseline (MMDs and AMDs P < 0.001, NRS score P = 0.005). Over the same time frame, 18 (56%) patients maintained a >= 50% reduction from baseline in MMDs. At week 4 after treatment completion, 10 (31%) patients restarted treatment due to disease rebound to baseline levels. Conclusions More than half patients had an early disease worsening, while the remaining patients maintained their responder status during weeks 1-4 after treatment completion. Further studies might identify predictors of prolonged response to erenumab and define the optimal treatment duration according to patients' characteristics.
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