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dc.contributor.authorVaury, Alexandra
dc.contributor.authorYapici, Zuhal
dc.contributor.authorFan, Jenna
dc.contributor.authorPelov, Diana
dc.contributor.authorFrench, Jacqueline A.
dc.contributor.authorFranz, David N.
dc.contributor.authorLawson, John A.
dc.contributor.authorIkeda, Hiroko
dc.contributor.authorPolster, Tilman
dc.contributor.authorNabbout, Rima
dc.contributor.authorCuratolo, Paolo
dc.contributor.authorde Vries, Petrus J.
dc.contributor.authorDlugos, Dennis J.
dc.contributor.authorVoi, Maurizio
dc.date.accessioned2021-03-05T17:32:16Z
dc.date.available2021-03-05T17:32:16Z
dc.date.issued2018
dc.identifier.citationFranz D. N. , Lawson J. A. , Yapici Z., Ikeda H., Polster T., Nabbout R., Curatolo P., de Vries P. J. , Dlugos D. J. , Voi M., et al., "Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial", NEUROLOGY-CLINICAL PRACTICE, cilt.8, ss.412-420, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_c60e494c-2700-475d-adbd-b0ed449f291c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/131313
dc.identifier.urihttps://doi.org/10.1212/cpj.0000000000000514
dc.description.abstractBackgroundEXamining everolimus In a Study of Tuberous sclerosis 3 (EXIST-3) demonstrated significantly reduced seizure frequency (SF) with everolimus vs placebo. In this study, we evaluate the long-term efficacy and safety of everolimus for tuberous sclerosis complex (TSC)-associated treatment-refractory seizures.MethodsAfter completion of the core phase, patients could enter an open-label extension phase and receive everolimus (target exposure, 3-15 ng/mL) for 48 weeks. Efficacy end points included change from baseline in average weekly SF expressed as response rate (RR, 50% reduction) and median percentage reduction (PR).ResultsOf 366 patients, 361 received everolimus in core/extension phases. The RR was 31% (95% CI, 26.2-36.1; N = 352) at week 18, 46.6% (95% CI, 40.9-52.5; N = 298) at 1 year, and 57.7% (95% CI, 49.7-65.4; N = 163) at 2 years. Median PR in SF was 31.7% (95% CI, 28.5-36.1) at week 18, 46.7% (95% CI, 40.2-54) at 1 year, and 56.9% (95% CI, 50-68.4) at 2 years. Ninety-five patients (26.3%) discontinued everolimus before 2 years; 103 (28.5%) had <2 years of follow-up at study cutoff, and 40% were exposed to everolimus for 2 years. An analysis classifying discontinued patients as nonresponders showed an RR of 30.2% (95% CI, 25.5-35.2; N = 361) at week 18, 38.8% (95% CI, 33.7-44.1; N = 358) at 1 year, and 41% (95% CI, 34.6-47.7; N = 229) at 2 years, suggesting sustained benefit over time. The incidence of grade 3/4 adverse events (AEs) (any cause) was 40.2%, and 13% discontinued because of AEs (pneumonia [1.7%] and stomatitis [1.4%]). Two deaths were suspected to be treatment-related (pneumonia and septic shock).ConclusionsSustained reductions in TSC-associated treatment-refractory seizures over time were achieved with adjunctive everolimus. The safety profile was consistent with the core phase with no new safety concerns.Classification of evidenceThis study provides Class IV evidence that long-term everolimus therapy reduces SF in patients with TSC-associated treatment-refractory seizures.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleEverolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial
dc.typeMakale
dc.relation.journalNEUROLOGY-CLINICAL PRACTICE
dc.contributor.departmentCincinnati Children''s Hospital Medical Center , ,
dc.identifier.volume8
dc.identifier.issue5
dc.identifier.startpage412
dc.identifier.endpage420
dc.contributor.firstauthorID257354


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