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Phase II study of everolimus for recurrent or progressive pediatric ependymoma.
Bowers, Daniel C; Rajaram, Veena; Karajannis, Matthias A; Gardner, Sharon L; Su, Jack Meng-Fen; Baxter, Patricia; Partap, Sonia; Klesse, Laura J.
Afiliación
  • Bowers DC; Harold C. Simmons Comprehensive Cancer Center and the Department of Pediatrics, University of Texas Southwestern Medical School, Dallas, TX, USA.
  • Rajaram V; Department of Pathology, University of Texas Southwestern Medical School, Dallas, TX, USA.
  • Karajannis MA; Department of Pediatrics, Memorial Sloan Kettering Cancer Center New York, NY, USA.
  • Gardner SL; Laura and Isaac Perlmutter Cancer Center at NYU Langone, New York, NY, USA.
  • Su JM; Baylor College of Medicine/Dan L. Duncan Comprehensive Cancer Center, Houston, TX, USA.
  • Baxter P; Baylor College of Medicine/Dan L. Duncan Comprehensive Cancer Center, Houston, TX, USA.
  • Partap S; Departments of Neurology and Pediatrics, Stanford University, Stanford, CA, USA.
  • Klesse LJ; Harold C. Simmons Comprehensive Cancer Center and the Department of Pediatrics, University of Texas Southwestern Medical School, Dallas, TX, USA.
Neurooncol Adv ; 5(1): vdad011, 2023.
Article en En | MEDLINE | ID: mdl-36950217
Background: Preclinical studies have suggested that mTOR pathway signaling may be a potential therapeutic target for childhood ependymoma. Methods: A phase II clinical trial (ClinicalTrials.gov identifier: NCT02155920) of single-agent everolimus was performed to test the hypothesis that mTOR pathway inhibition would result in tumor responses for children with recurrent and/or progressive ependymomas. Results: Eleven subjects [sex: 4 females (36.4%); median age: 8 years (range: 2-15 years); race: 9 white; prior therapies: median 6 (range: 3-9)] were enrolled on the study. Ten primary tumors were located in the posterior fossa and one primary tumor was located in the spinal cord. Eight of 9 tumors were PF-A subtype epenydmomas. All subjects were treated with oral everolimus 4.5 mg/m2/day (each cycle = 28 days) that was titrated to achieve serum trough levels of 5-15 ng/ml. Overall, everolimus was well tolerated; except for a single event of grade 3 pneumonia, all adverse events were grade 1-2. No objective tumor responses were observed. Participating subjects experienced tumor progression and discontinued therapy after a median of 2 cycles of therapy (1 cycle = 2; 2 cycles = 6; 3, 4, and 8 cycles = 1 each). Conclusions: Everolimus does not appear to have activity for children with recurrent or progressive PF-A ependymoma.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurooncol Adv Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurooncol Adv Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido