# A comparative study on the efficacy of different combinational anti-seizure medication therapies following valproate monotherapy failure

**Authors:** Raowei Yan, Hesheng Zhang, Jia He, Wenyu Liu, Nanya Hao, Enhui Zhang, Yujie Chen, Zhujing Ou, Xintong Wu, Dong Zhou

PMC · DOI: 10.1186/s42494-025-00233-3 · Acta Epileptologica · 2025-10-14

## TL;DR

This study compares the effectiveness of adding different anti-seizure medications to valproate for patients with epilepsy who do not respond to valproate alone.

## Contribution

The study provides real-world evidence on the comparative efficacy of add-on therapies after valproate monotherapy failure.

## Key findings

- Lamotrigine showed higher efficacy for generalized epilepsy compared to levetiracetam, topiramate, and carbamazepine.
- Oxcarbazepine was more effective for focal epilepsy than levetiracetam, topiramate, and carbamazepine.
- Response rates varied significantly across medication combinations and seizure types.

## Abstract

Sodium valproate (VPA) is widely recognized as the first-line treatment for patients with epilepsy (PWE). However, current studies lack evidence to determine the best add-on medication following VPA monotherapy failure. Lamotrigine (LTG), levetiracetam (LEV), oxcarbazepine (OXC), topiramate (TPM), and carbamazepine (CBZ) also exhibit broad-spectrum activity for seizures. This study aims to compare the therapeutic efficacy of different anti-seizure medication combinations in PWE following valproate monotherapy failure.

Individuals were categorized into five groups: VPA + LTG, VPA + LEV, VPA + TPM, VPA + OXC and VPA + CBZ. Each group was further subdivided based on seizure type: generalized onset, focal onset, or unknown onset. The effectiveness of these five groups was compared using variance, χ2 test and Kaplan–Meier survival analysis.

A total of 2656 PWEs were included in this study. The ≥ 50% response rates for subjects with generalized epilepsy when combining VPA with LTG, OXC, LEV, TPM, and CBZ were 89.6%, 81.0%, 77.9%, 77.7%, and 75.9%, respectively. The LTG group demonstrated significantly higher efficacy than the LEV, TPM, and CBZ groups (P < 0.05). The ≥ 50% response rate of LTG, OXC, LEV, TPM and CBZ for subjects with focal epilepsy were 86.3%, 88.9%, 79.3%, 75.9% and 74.8%, respectively; with the OXC group being significantly more effective than the LEV, TPM, and CBZ groups (P < 0.05).

In this real-world study, we assessed the effectiveness of five anti-seizure medications as add-on therapy for PWE who failed sodium valproate monotherapy. Our findings suggest that combining LTG may be more effective for subjects with generalized epilepsy, while combining OXC may be more effective for subjects with focal epilepsy.

## Linked entities

- **Chemicals:** sodium valproate (PubChem CID 16760703), lamotrigine (PubChem CID 3878), levetiracetam (PubChem CID 5284583), oxcarbazepine (PubChem CID 34312), topiramate (PubChem CID 5284627), carbamazepine (PubChem CID 2554)
- **Diseases:** epilepsy (MONDO:0005027)

## Full-text entities

- **Diseases:** focal epilepsy (MESH:D004828), seizure (MESH:D012640), PWE (MESH:D004827)
- **Chemicals:** LEV (MESH:D000077287), OXC (MESH:D000078330), Sodium valproate (MESH:D014635), CBZ (MESH:D002220), LTG (MESH:D000077213), TPM (MESH:D000077236)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12519853