Literature DB >> 27799506

Personalized Treatment for a Patient With a BRAF V600E Mutation Using Dabrafenib and a Tumor Treatment Fields Device in a High-Grade Glioma Arising From Ganglioglioma.

Silviya K Meletath1, Dean Pavlick1, Tim Brennan1, Roy Hamilton1, Juliann Chmielecki1, Julia A Elvin1, Norma Palma1, Jeffrey S Ross1,1, Vincent A Miller1, Philip J Stephens1, George Snipes1, Veena Rajaram1, Siraj M Ali1, Isaac Melguizo-Gavilanes1.   

Abstract

BACKGROUND: Gangliogliomas are slow-growing, low-grade central nervous system tumors affecting children and young adults. However, some patients will experience tumor recurrence and/or malignant progression. This article reports on the clinical history, molecular findings, and treatment response in a patient with BRAF V600-mutated high-grade glioma arising from ganglioglioma.
METHODS: Hematoxylin-eosin staining and comprehensive genomic profiling via Foundation One were performed on the tumor sample from a male patient undergoing treatment at the Department of Neuro-Oncology at Baylor University Medical Center.
RESULTS: The patient was eligible for participation in a clinical trial (ClinicalTrials.gov identifier: NCT00916409) of a tumor treatment fields (TTFields) device, NovoTTF-100A, with concurrent radiation and chemotherapy (CCRT). His disease relapsed 4 months after completion of his CCRT, with MRI showing areas of enhancement. Temozolomide was discontinued and he was offered dabrafenib, an oral selective inhibitor of BRAF V600E, with continued use of NovoTTF. At the time of this report, after 2 years of treatment with dabrafenib and TTFields, the patient shows a durable complete response in all areas with no active lesions or new areas of enhancement.
CONCLUSIONS: This report suggests that TTFields delivered in combination with targeted therapy dabrafenib yielded a remarkable clinical and radiologic response in this recurrent high-grade glioma. Targeted therapy matched to genomic alterations combined with TTFields treatment could provide clinical benefit and should be prospectively explored in the near future.
Copyright © 2016 by the National Comprehensive Cancer Network.

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Year:  2016        PMID: 27799506     DOI: 10.6004/jnccn.2016.0145

Source DB:  PubMed          Journal:  J Natl Compr Canc Netw        ISSN: 1540-1405            Impact factor:   11.908


  10 in total

1.  Efficacy of Dabrafenib for three children with brainstem BRAFV600E positive ganglioglioma.

Authors:  Laflamme Philippe; Kondyli Maria; Aljared Tariq; Miconiatis Sofia; Saint-Martin Christine; Farmer Jean-Pierre; Roy W Dudley; Perreault Sébastien; Jabado Nada; Larouche Valérie
Journal:  J Neurooncol       Date:  2019-09-09       Impact factor: 4.130

2.  Dabrafenib in patients with recurrent, BRAF V600E mutated malignant glioma and leptomeningeal disease.

Authors:  Michael C Burger; Michael W Ronellenfitsch; Nadja I Lorenz; Marlies Wagner; Martin Voss; David Capper; Theophilos Tzaridis; Ulrich Herrlinger; Joachim P Steinbach; Gabriele Stoffels; Karl-Josef Langen; Christian Brandts; Christian Senft; Patrick N Harter; Oliver Bähr
Journal:  Oncol Rep       Date:  2017-10-02       Impact factor: 3.906

3.  Dabrafenib Treatment in a Patient with an Epithelioid Glioblastoma and BRAF V600E Mutation.

Authors:  Garry Ceccon; Jan-Michael Werner; Veronika Dunkl; Caroline Tscherpel; Gabriele Stoffels; Anna Brunn; Martina Deckert; Gereon R Fink; Norbert Galldiks
Journal:  Int J Mol Sci       Date:  2018-04-05       Impact factor: 5.923

4.  Clinical Relevance of BRAF V600E Mutation Status in Brain Tumors with a Focus on a Novel Management Algorithm.

Authors:  Adam Kowalewski; Justyna Durślewicz; Marek Zdrenka; Dariusz Grzanka; Łukasz Szylberg
Journal:  Target Oncol       Date:  2020-08       Impact factor: 4.493

Review 5.  BRAF Mutations and the Utility of RAF and MEK Inhibitors in Primary Brain Tumors.

Authors:  Karisa C Schreck; Stuart A Grossman; Christine A Pratilas
Journal:  Cancers (Basel)       Date:  2019-08-28       Impact factor: 6.639

6.  Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases.

Authors:  Matthew Smith-Cohn; Christian Davidson; Howard Colman; Adam L Cohen
Journal:  CNS Oncol       Date:  2019-12-10

7.  Case Report: Multi-Orifices Vertebral Arteriovenous Fistula With Severe Scoliosis in Neurofibromatosis Type 1: Might Be a Congenital Disease With Mesodermal Dysplasia.

Authors:  Yingjin Wang; Changwei Yuan; Shengli Shen; Yang Zhang; Jiayong Zhang; Hongzhou Duan
Journal:  Front Neurol       Date:  2021-03-17       Impact factor: 4.003

Review 8.  Tumor-Treating Fields in Glioblastomas: Past, Present, and Future.

Authors:  Xiaopeng Guo; Xin Yang; Jiaming Wu; Huiyu Yang; Yilin Li; Junlin Li; Qianshu Liu; Chen Wu; Hao Xing; Penghao Liu; Yu Wang; Chunhua Hu; Wenbin Ma
Journal:  Cancers (Basel)       Date:  2022-07-28       Impact factor: 6.575

9.  Prediction of BRAF mutation status in glioblastoma multiforme by preoperative ring enhancement appearances on MRI.

Authors:  Xiaomin Cai; Zheng Chen; Bowen Chang; Ming Tu; Shiting Li; Xuhui Wang; Ming Chen
Journal:  Front Oncol       Date:  2022-08-08       Impact factor: 5.738

10.  Targetable BRAF and RAF1 Alterations in Advanced Pediatric Cancers.

Authors:  Andrew Rankin; Adrienne Johnson; Alison Roos; Geoffrey Kannan; Jeffrey Knipstein; Nicholas Britt; Mark Rosenzweig; James Haberberger; Dean Pavlick; Eric Severson; Jo-Anne Vergilio; Rachel Squillace; Rachel Erlich; Pratheesh Sathyan; Stuart Cramer; David Kram; Jeffrey Ross; Vince Miller; Prasanth Reddy; Brian Alexander; Siraj M Ali; Shakti Ramkissoon
Journal:  Oncologist       Date:  2020-09-25
  10 in total

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