Seizure prophylaxis in glioma surgery (SPRING): a multi-centre, unblinded, randomised trial

Background50-80% of all glioma patients will have seizures. Guidelines recommend against prophylactic anti-seizure medication, but levetiracetam is frequently prescribed. Our aim was to determine the effectiveness of 12-months prophylactic levetiracetam at reducing seizure risk. MethodsSeizure-naive patients undergoing glioma surgery were randomised (1:1) to 12-months levetiracetam or no prophylaxis and followed until death or maximum 18-months. The primary outcome was one-year risk of first seizure. Patients who died within 12-months of randomisation without experiencing a seizure were excluded from the primary outcome analysis. Target accrual was 804 participants. The trial was registered (ISRCTN 49474281 and EudraCT 2018-001312-30). ResultsBetween Oct 10, 2019 and Aug 30, 2022, 96 patients, from 24 to 79 years of age, were randomised to levetiracetam (n=49) or no prophylaxis (n=47). The trial closed early due to slow accrual and the Covid pandemic. In the levetiracetam group 17 patients had a seizure and 32 did not (19 survived [≥] 12-months, 13 died within 12-months). In the no prophylaxis group 15 patients had a seizure and 30 did not (21 survived [≥]12-months, 9 died within 12-months). Seventeen of the 36 evaluable levetiracetam patients (47%) had a seizure, compared with 15 of 36 evaluable no prophylaxis patients (41%) (OR 1.25, 95%CI 0.49-3.21, p=0.64). There were no levetiracetam related serious adverse events. ConclusionsThe SPRING trial provides no evidence of a difference between levetiracetam and no prophylaxis in the 12-month seizure risk in patients undergoing glioma surgery, but the study was underpowered. The role of prophylactic anti-seizure medication remains undefined.