dc.contributor.author | Herbst, Fabian | |
dc.contributor.author | French, Jacqueline A. | |
dc.contributor.author | Dlugos, Dennis J. | |
dc.contributor.author | Peyrard, Severine | |
dc.contributor.author | Pelov, Diana | |
dc.contributor.author | Franz, David N. | |
dc.contributor.author | Lawson, John A. | |
dc.contributor.author | Yapici, Zuhal | |
dc.contributor.author | Ikeda, Hiroko | |
dc.contributor.author | Polster, Tilman | |
dc.contributor.author | Nabbout, Rima | |
dc.contributor.author | Curatolo, Paolo | |
dc.contributor.author | Vries, Petrus J. | |
dc.date.accessioned | 2021-12-10T10:31:53Z | |
dc.date.available | 2021-12-10T10:31:53Z | |
dc.identifier.citation | Franz D. N. , Lawson J. A. , Yapici Z., Ikeda H., Polster T., Nabbout R., Curatolo P., Vries P. J. , Dlugos D. J. , Herbst F., et al., "Adjunctive everolimus therapy for tuberous sclerosis complex-associated refractory seizures: Results from the postextension phase of EXIST-3", EPILEPSIA, 2021 | |
dc.identifier.issn | 0013-9580 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_45bcf862-4ff8-49be-a5c3-f35d82446303 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/170079 | |
dc.identifier.uri | https://doi.org/10.1111/epi.17099 | |
dc.description.abstract | Objective Epilepsy is highly prevalent in patients with tuberous sclerosis complex (TSC). Everolimus showed higher efficacy than placebo for seizures in the primary analysis of the EXIST-3 study. Here, we present the long-term outcomes of everolimus at the end of the postextension phase (PEP; data cutoff date: October 25, 2017). Methods After completion of the extension phase, patients were invited to continue everolimus in the PEP with everolimus (targeted trough concentration = 5-15 ng/ml, investigator-judged). Efficacy assessments included changes in seizure status during the PEP collected at 12-week intervals as parent/caregiver-reported data through a structured questionnaire. Results Among 361 patients, 343 entered the extension phase and 249 entered the PEP. After 12 weeks in the PEP, 18.9% (46/244) of patients were seizure-free since the last visit of the extension phase and 64.8% (158/244) had a stable/improved seizure status. At 24 weeks, the corresponding percentages were 18.2% (42/231) and 64.5% (149/231). Among 244 patients, the response rate was 32.8% (80/244) during the 12-week maintenance period of the core phase and 63.9% (156/244) at the end of the extension phase. Of the 149 responders at the end of the extension phase, 70.5% were seizure-free or had stable/improved seizure status. Long-term efficacy data showed persistent responses were observed in 183 of 361 patients (50.7%); 63.9% of these patients had a response that lasted at least 48 weeks. The most frequent Grade 3-4 adverse events (>= 2% incidence) reported throughout the study were pneumonia, status epilepticus, seizure, stomatitis, neutropenia, and gastroenteritis. Four patients died during the study. Significance The final analysis of EXIST-3 demonstrated the sustained efficacy of everolimus as adjunctive therapy in patients with TSC-associated treatment-refractory seizures, with a tolerable safety profile. | |
dc.language.iso | eng | |
dc.subject | Neurology | |
dc.subject | Neurology (clinical) | |
dc.subject | Life Sciences | |
dc.subject | Health Sciences | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Nöroloji | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | KLİNİK NEUROLOJİ | |
dc.title | Adjunctive everolimus therapy for tuberous sclerosis complex-associated refractory seizures: Results from the postextension phase of EXIST-3 | |
dc.type | Makale | |
dc.relation.journal | EPILEPSIA | |
dc.contributor.department | Cincinnati Childrens Hosp Med Ctr , , | |
dc.contributor.firstauthorID | 2758029 | |