Objective: The purpose of this literature study was to evaluate the effect of perampanel as an adjunct therapy in patients, 12 years of age or older suffering from pharmacoresistant epilepsy. Methods: This thesis is a literature work based on scientific articles sought and obtained from the medical database PubMed. The five articles were selected with the criteria that perampanel is used for therapy-resistant epilepsy, as an adjunct therapy in patients who do not respond to other anti-epileptic drugs, in patients using 1-3 antiepileptic drugs, participants 12 years or older and the drug is used in humans. The result measured was the percentage change in seizure rate per 28 days and ≥ 50% responder rate. Results: Study 1 and 5 compared the effect and safety of different doses of perampanel with placebo. A statistically significant change in seizure rates was shown in the perampanel group, 34.5% for 8 mg/day and 26.3% for 12 mg/day, compared to placebo 21.0%. The impact of perampanel in study 5 also showed a statistically significant difference in responder rate in perampanel group, 64.2% compared to placebo 39.5%, study 1 showed no statistically significant difference here. Study 2 evaluated the safety and tolerability of long-term treatment of perampanel up to 12 mg/day. In each 13-week interval of perampanel treatment, the overall median percentage reduction was 39.3% for 14-26 weeks (n=1,114), 46.5% for weeks 40-52 (n=731) and 58.1% for weeks 92104 (n=59). Similarly, in the case of the decrease in the responder rate of 41.4%, 46.9% and 62.7% for the respective 13-week intervals. Study 3 compared the efficacy and safety of perampanel with placebo. A statistically significant change in seizure rates was shown in perampanel group, -34.8% for 8 mg/day and -35.6% for 12 mg/day compared to placebo who had -18.0%. An increase of the 50% responder rate was also seen in the perampanel group, 40.9% for 8 mg/day and 45.0% for 12 mg/day. In Study 4, the effect and safety of perampanel were evaluated in patients who had received placebo in previous Phase III double-blinded core studies and switched to perampanel in extension study 307. The percentage decrease in the overall seizure rate in double blinded studies increased from 18.6% to 44.3% for placebo group and from 31.7% to 41.4% for perampanel group. Responder rate for placebo was 20.3% increased to 44.3% and perampanel was 34.0% increased to 43.4% in the double blinded studies. Conclusions: All included studies analyzed the effect on seizure frequency, tolerability and adverse reactions. Studies 1–5 showed a clear decrease in seizure rates. But it was also found that there were differences between the youth group and the study pool both as a whole as well as at different doses. The question in this literature study can thus be answered with yes, perampanel has a positive effect as an adjunct therapy against therapy-resistant epilepsy. However, it is of great importance that the dose and titration are adjusted individually.
| Identifer | oai:union.ndltd.org:UPSALLA1/oai:DiVA.org:lnu-93360 |
| Date | January 2020 |
| Creators | Wiking, Margie |
| Publisher | Linnéuniversitetet, Institutionen för kemi och biomedicin (KOB) |
| Source Sets | DiVA Archive at Upsalla University |
| Language | Swedish |
| Detected Language | English |
| Type | Student thesis, info:eu-repo/semantics/bachelorThesis, text |
| Format | application/pdf |
| Rights | info:eu-repo/semantics/openAccess |
Page generated in 0.0022 seconds