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Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial
BACKGROUND: EXamining 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-ref...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276348/ https://www.ncbi.nlm.nih.gov/pubmed/30564495 http://dx.doi.org/10.1212/CPJ.0000000000000514 |
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author | Franz, David N. Lawson, John A. Yapici, Zuhal Ikeda, Hiroko Polster, Tilman Nabbout, Rima Curatolo, Paolo de Vries, Petrus J. Dlugos, Dennis J. Voi, Maurizio Fan, Jenna Vaury, Alexandra Pelov, Diana French, Jacqueline A. |
author_facet | Franz, David N. Lawson, John A. Yapici, Zuhal Ikeda, Hiroko Polster, Tilman Nabbout, Rima Curatolo, Paolo de Vries, Petrus J. Dlugos, Dennis J. Voi, Maurizio Fan, Jenna Vaury, Alexandra Pelov, Diana French, Jacqueline A. |
author_sort | Franz, David N. |
collection | PubMed |
description | BACKGROUND: EXamining 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. METHODS: After 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). RESULTS: Of 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). CONCLUSIONS: Sustained 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 EVIDENCE: This study provides Class IV evidence that long-term everolimus therapy reduces SF in patients with TSC-associated treatment-refractory seizures. |
format | Online Article Text |
id | pubmed-6276348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-62763482018-12-18 Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial Franz, David N. Lawson, John A. Yapici, Zuhal Ikeda, Hiroko Polster, Tilman Nabbout, Rima Curatolo, Paolo de Vries, Petrus J. Dlugos, Dennis J. Voi, Maurizio Fan, Jenna Vaury, Alexandra Pelov, Diana French, Jacqueline A. Neurol Clin Pract Research BACKGROUND: EXamining 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. METHODS: After 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). RESULTS: Of 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). CONCLUSIONS: Sustained 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 EVIDENCE: This study provides Class IV evidence that long-term everolimus therapy reduces SF in patients with TSC-associated treatment-refractory seizures. Lippincott Williams & Wilkins 2018-10 /pmc/articles/PMC6276348/ /pubmed/30564495 http://dx.doi.org/10.1212/CPJ.0000000000000514 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Research Franz, David N. Lawson, John A. Yapici, Zuhal Ikeda, Hiroko Polster, Tilman Nabbout, Rima Curatolo, Paolo de Vries, Petrus J. Dlugos, Dennis J. Voi, Maurizio Fan, Jenna Vaury, Alexandra Pelov, Diana French, Jacqueline A. Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial |
title | Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial |
title_full | Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial |
title_fullStr | Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial |
title_full_unstemmed | Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial |
title_short | Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial |
title_sort | everolimus for treatment-refractory seizures in tsc: extension of a randomized controlled trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276348/ https://www.ncbi.nlm.nih.gov/pubmed/30564495 http://dx.doi.org/10.1212/CPJ.0000000000000514 |
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