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Long-Term Use of Everolimus in Patients with Tuberous Sclerosis Complex: Final Results from the EXIST-1 Study.
Franz, David N; Belousova, Elena; Sparagana, Steven; Bebin, E Martina; Frost, Michael D; Kuperman, Rachel; Witt, Olaf; Kohrman, Michael H; Flamini, J Robert; Wu, Joyce Y; Curatolo, Paolo; de Vries, Petrus J; Berkowitz, Noah; Niolat, Julie; Józwiak, Sergiusz.
Afiliación
  • Franz DN; Department of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Belousova E; Department of Pediatrics, Research and Clinical Institute of Pediatrics, Pirogov Russian National Research Medical University, Moscow, Russia.
  • Sparagana S; Department of Neurology, Texas Scottish Rite Hospital for Children, Dallas, Texas, United States of America.
  • Bebin EM; Department of Neurology, University of Alabama School of Medicine, Birmingham, Alabama, United States of America.
  • Frost MD; Department of Neurology, Minnesota Epilepsy Group, St. Paul, Minnesota, United States of America.
  • Kuperman R; Department of Neurology, Children's Hospital and Research Center, Oakland, California, United States of America.
  • Witt O; Department of Oncology, University of Heidelberg Medical Center and German Cancer Research Center, Heidelberg, Germany.
  • Kohrman MH; Department of Neurology, University of Chicago, Chicago, Illinois, United States of America.
  • Flamini JR; Department of Neurology, Children's Healthcare of Atlanta, Atlanta, Georgia, United States of America.
  • Wu JY; Department of Neurology, Mattel Children's Hospital at the University of California Los Angeles, Los Angeles, California, United States of America.
  • Curatolo P; Department of Neurology, University of Rome Tor Vergata, Rome, Italy.
  • de Vries PJ; Department of Psychiatry and Mental Health, Division of Child & Adolescent Psychiatry, University of Cape Town, Cape Town, South Africa.
  • Berkowitz N; Department of Oncology, Novartis Pharmaceuticals Corporation, East Hanover, New Jersey, United States of America.
  • Niolat J; Department of Oncology, Novartis Pharmaceuticals S.A.S., Rueil-Malmaison, France.
  • Józwiak S; Department of Pediatric Neurology, Medical University of Warsaw, Warsaw, Poland.
PLoS One ; 11(6): e0158476, 2016.
Article en En | MEDLINE | ID: mdl-27351628
BACKGROUND: Everolimus, a mammalian target of rapamycin (mTOR) inhibitor, has demonstrated efficacy in treating subependymal giant cell astrocytomas (SEGAs) and other manifestations of tuberous sclerosis complex (TSC). However, long-term use of mTOR inhibitors might be necessary. This analysis explored long-term efficacy and safety of everolimus from the conclusion of the EXIST-1 study (NCT00789828). METHODS AND FINDINGS: EXIST-1 was an international, prospective, double-blind, placebo-controlled phase 3 trial examining everolimus in patients with new or growing TSC-related SEGA. After a double-blind core phase, all remaining patients could receive everolimus in a long-term, open-label extension. Everolimus was initiated at a dose (4.5 mg/m2/day) titrated to a target blood trough of 5-15 ng/mL. SEGA response rate (primary end point) was defined as the proportion of patients achieving confirmed ≥50% reduction in the sum volume of target SEGA lesions from baseline in the absence of worsening nontarget SEGA lesions, new target SEGA lesions, and new or worsening hydrocephalus. Of 111 patients (median age, 9.5 years) who received ≥1 dose of everolimus (median duration, 47.1 months), 57.7% (95% confidence interval [CI], 47.9-67.0) achieved SEGA response. Of 41 patients with target renal angiomyolipomas at baseline, 30 (73.2%) achieved renal angiomyolipoma response. In 105 patients with ≥1 skin lesion at baseline, skin lesion response rate was 58.1%. Incidence of adverse events (AEs) was comparable with that of previous reports, and occurrence of emergent AEs generally decreased over time. The most common AEs (≥30% incidence) suspected to be treatment-related were stomatitis (43.2%) and mouth ulceration (32.4%). CONCLUSIONS: Everolimus use led to sustained reduction in tumor volume, and new responses were observed for SEGA and renal angiomyolipoma from the blinded core phase of the study. These findings support the hypothesis that everolimus can safely reverse multisystem manifestations of TSC in a significant proportion of patients. TRIAL REGISTRATION: ClinicalTrials.gov NCT00789828.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Tuberosa / Inhibidores de Proteínas Quinasas / Everolimus / Antineoplásicos Tipo de estudio: Clinical_trials Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Tuberosa / Inhibidores de Proteínas Quinasas / Everolimus / Antineoplásicos Tipo de estudio: Clinical_trials Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos