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Targeted MAPK Pathway Inhibitors in Patients With Disseminated Pilocytic Astrocytomas.
Drobysheva, Anastasia; Klesse, Laura J; Bowers, Daniel C; Rajaram, Veena; Rakheja, Dinesh; Timmons, Charles F; Wang, Jason; Koral, Korgun; Gargan, Lynn; Ramos, Erica; Park, Jason Y.
Afiliación
  • Drobysheva A; Department of Pathology, University of Texas Southwestern Medical Center
  • Klesse LJ; Department of Pathology and Laboratory Medicine, Children's Health
  • Bowers DC; Department of Pediatrics, University of Texas Southwestern Medical Center
  • Rajaram V; Department of Pediatrics, Children's Health
  • Rakheja D; Department of Pediatrics, University of Texas Southwestern Medical Center
  • Timmons CF; Department of Pediatrics, Children's Health
  • Wang J; Department of Pathology, University of Texas Southwestern Medical Center
  • Koral K; Department of Pathology and Laboratory Medicine, Children's Health
  • Gargan L; Department of Pathology, University of Texas Southwestern Medical Center
  • Ramos E; Department of Pathology and Laboratory Medicine, Children's Health
  • Park JY; Department of Pediatrics, University of Texas Southwestern Medical Center
J Natl Compr Canc Netw ; 15(8): 978-982, 2017 08.
Article en En | MEDLINE | ID: mdl-28784858
This report presents a series of 5 pediatric patients with disseminated pilocytic astrocytomas and frequent nonfusion activating mutations. Genetic variants in these patients' tumors include BRAF p.Val600Glu, BRAF p.Val600Asp, and KRAS p.Gly60_Gln62ins7. The 2 patients with BRAF-mutated tumors were treated with dabrafenib or a combination of dabrafenib plus trametinib. The patients had either near complete resolution of the primary tumor (BRAF p.Val600Glu) or a stable primary tumor (BRAF p.Val600Asp). Both patients showed improvement in leptomeningeal dissemination without significant toxicity. Genomic testing of disseminated pilocytic astrocytomas, particularly those arising at extracerebellar locations, may result in the identification of mutations associated with ERK/MAPK activation. Patients with these activating mutations may benefit from targeted therapies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Astrocitoma / Sistema de Señalización de MAP Quinasas / Inhibidores de Proteínas Quinasas / Terapia Molecular Dirigida / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Natl Compr Canc Netw Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Astrocitoma / Sistema de Señalización de MAP Quinasas / Inhibidores de Proteínas Quinasas / Terapia Molecular Dirigida / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Natl Compr Canc Netw Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article