Real-world analysis of retention on cenobamate in patients with epilepsy in the United States

This retrospective, observational study used US claims data to assess retention rates on cenobamate compared with four branded antiseizure medications (ASMs) in patients with epilepsy. Adults (≥18 years) with prevalent epilepsy (ICD-10 code G40.xx) and ≥ 1 prescription for cenobamate or any of the n...

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Veröffentlicht in:Epilepsy research 2023-11, Vol.197, p.107207-107207, Article 107207
Hauptverfasser: Stern, Sean, Weingarten, Mindl, Mandapati, Sudhakar, Ferrari, Louis, Wade, Clarence T.
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container_end_page 107207
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container_start_page 107207
container_title Epilepsy research
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creator Stern, Sean
Weingarten, Mindl
Mandapati, Sudhakar
Ferrari, Louis
Wade, Clarence T.
description This retrospective, observational study used US claims data to assess retention rates on cenobamate compared with four branded antiseizure medications (ASMs) in patients with epilepsy. Adults (≥18 years) with prevalent epilepsy (ICD-10 code G40.xx) and ≥ 1 prescription for cenobamate or any of the newer branded ASMs (brivaracetam, eslicarbazepine, lacosamide, or perampanel) between May 1, 2020 and December 31, 2021 were identified from the HealthVerity Marketplace database. At least 360 days of continuous enrollment was required before and after the index date (Day 1 of initiating cenobamate or branded ASM). Patients were followed until cessation of cenobamate or branded ASM or the end of data collection using Kaplan-Meier methods. Retention was compared between cenobamate and the branded ASMs (both as a group and individually) using Chi-square tests. In total, 4109 patients were included (195 cenobamate; 3914 branded ASMs). A higher proportion of patients in the cenobamate group compared with the branded ASMs group had concurrent focal and generalized epilepsy (65.6% vs 40.0%) and were on ≥ 3 concomitant ASMs (48.2% vs 12.8%) at the index date. Median time to discontinuation (i.e., the time that half the patients discontinued) was not quite reached after 12 months in the cenobamate group (50.3% of patients remained on cenobamate) and was 7.7 months in the branded ASMs group. Retention was significantly higher with cenobamate vs the branded ASMs group (p = 0.04545) and vs the individual ASMs lacosamide (p = 0.03044) and perampanel (p = 0.01558). Twelve-month retention rates (95% confidence intervals) were 50.3% (43.1%−57.0%) for cenobamate, 40.5% (38.9%−42.0%) for branded ASMs overall, 42.3% (38.6%−46.0%) for brivaracetam, 44.1% (39.2%−49.0%) for eslicarbazepine, 39.9% (38.0%−41.8%) for lacosamide, and 36.8% (31.9%−41.8%) for perampanel. In this real-world analysis, retention was significantly higher with cenobamate vs a pooled group of four branded ASMs despite a greater frequency of patients in the cenobamate group having characteristics of more difficult-to-treat epilepsy. •Retention on cenobamate was significantly higher vs branded ASMs per US claims data.•Branded ASMs included brivaracetam, eslicarbazepine, lacosamide, and perampanel.•Retention was significantly higher for cenobamate vs lacosamide and perampanel.
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Median time to discontinuation (i.e., the time that half the patients discontinued) was not quite reached after 12 months in the cenobamate group (50.3% of patients remained on cenobamate) and was 7.7 months in the branded ASMs group. Retention was significantly higher with cenobamate vs the branded ASMs group (p = 0.04545) and vs the individual ASMs lacosamide (p = 0.03044) and perampanel (p = 0.01558). Twelve-month retention rates (95% confidence intervals) were 50.3% (43.1%−57.0%) for cenobamate, 40.5% (38.9%−42.0%) for branded ASMs overall, 42.3% (38.6%−46.0%) for brivaracetam, 44.1% (39.2%−49.0%) for eslicarbazepine, 39.9% (38.0%−41.8%) for lacosamide, and 36.8% (31.9%−41.8%) for perampanel. 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Median time to discontinuation (i.e., the time that half the patients discontinued) was not quite reached after 12 months in the cenobamate group (50.3% of patients remained on cenobamate) and was 7.7 months in the branded ASMs group. Retention was significantly higher with cenobamate vs the branded ASMs group (p = 0.04545) and vs the individual ASMs lacosamide (p = 0.03044) and perampanel (p = 0.01558). Twelve-month retention rates (95% confidence intervals) were 50.3% (43.1%−57.0%) for cenobamate, 40.5% (38.9%−42.0%) for branded ASMs overall, 42.3% (38.6%−46.0%) for brivaracetam, 44.1% (39.2%−49.0%) for eslicarbazepine, 39.9% (38.0%−41.8%) for lacosamide, and 36.8% (31.9%−41.8%) for perampanel. 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Adults (≥18 years) with prevalent epilepsy (ICD-10 code G40.xx) and ≥ 1 prescription for cenobamate or any of the newer branded ASMs (brivaracetam, eslicarbazepine, lacosamide, or perampanel) between May 1, 2020 and December 31, 2021 were identified from the HealthVerity Marketplace database. At least 360 days of continuous enrollment was required before and after the index date (Day 1 of initiating cenobamate or branded ASM). Patients were followed until cessation of cenobamate or branded ASM or the end of data collection using Kaplan-Meier methods. Retention was compared between cenobamate and the branded ASMs (both as a group and individually) using Chi-square tests. In total, 4109 patients were included (195 cenobamate; 3914 branded ASMs). A higher proportion of patients in the cenobamate group compared with the branded ASMs group had concurrent focal and generalized epilepsy (65.6% vs 40.0%) and were on ≥ 3 concomitant ASMs (48.2% vs 12.8%) at the index date. Median time to discontinuation (i.e., the time that half the patients discontinued) was not quite reached after 12 months in the cenobamate group (50.3% of patients remained on cenobamate) and was 7.7 months in the branded ASMs group. Retention was significantly higher with cenobamate vs the branded ASMs group (p = 0.04545) and vs the individual ASMs lacosamide (p = 0.03044) and perampanel (p = 0.01558). Twelve-month retention rates (95% confidence intervals) were 50.3% (43.1%−57.0%) for cenobamate, 40.5% (38.9%−42.0%) for branded ASMs overall, 42.3% (38.6%−46.0%) for brivaracetam, 44.1% (39.2%−49.0%) for eslicarbazepine, 39.9% (38.0%−41.8%) for lacosamide, and 36.8% (31.9%−41.8%) for perampanel. In this real-world analysis, retention was significantly higher with cenobamate vs a pooled group of four branded ASMs despite a greater frequency of patients in the cenobamate group having characteristics of more difficult-to-treat epilepsy. •Retention on cenobamate was significantly higher vs branded ASMs per US claims data.•Branded ASMs included brivaracetam, eslicarbazepine, lacosamide, and perampanel.•Retention was significantly higher for cenobamate vs lacosamide and perampanel.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.eplepsyres.2023.107207</doi><tpages>1</tpages><orcidid>https://orcid.org/0009-0002-5266-8371</orcidid></addata></record>
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subjects Antiseizure medication
Cenobamate
Epilepsy
Real-world
Retention
title Real-world analysis of retention on cenobamate in patients with epilepsy in the United States
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