Literature DB >> 15851741

EGFR tyrosine kinase domain mutations in human gliomas.

Y Marie1, A F Carpentier, A M P Omuro, M Sanson, J Thillet, K Hoang-Xuan, J-Y Delattre.   

Abstract

Gefitinib is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor effective in patients with lung cancer with mutations in exons 19 and 21 of the EGFR tyrosine kinase domain. In this study, the authors tested the presence of such mutations in 95 gliomas including glioblastomas, anaplastic oligodendrogliomas, and low-grade gliomas. No mutation was found, which suggests that the biology of EGFR in gliomas is different from lung cancer and that this may be a factor in the resistance of glioblastomas to gefitinib.

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Year:  2005        PMID: 15851741     DOI: 10.1212/01.WNL.0000158654.07080.B0

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  20 in total

1.  Histone Deacetylase Inhibitors Resensitize EGFR/EGFRvIII-Overexpressing, Erlotinib-Resistant Glioblastoma Cells to Tyrosine Kinase Inhibition.

Authors:  Katrin Liffers; Katarina Kolbe; Manfred Westphal; Katrin Lamszus; Alexander Schulte
Journal:  Target Oncol       Date:  2016-02       Impact factor: 4.493

Review 2.  Challenges to targeting epidermal growth factor receptor in glioblastoma: escape mechanisms and combinatorial treatment strategies.

Authors:  Patrick Roth; Michael Weller
Journal:  Neuro Oncol       Date:  2014-10       Impact factor: 12.300

Review 3.  Towards personalized therapy for patients with glioblastoma.

Authors:  Katsuyuki Shirai; Arnab Chakravarti
Journal:  Expert Rev Anticancer Ther       Date:  2011-12       Impact factor: 4.512

4.  Safety and efficacy of erlotinib in first-relapse glioblastoma: a phase II open-label study.

Authors:  W K Alfred Yung; James J Vredenburgh; Timothy F Cloughesy; Phioanh Nghiemphu; Barbara Klencke; Mark R Gilbert; David A Reardon; Michael D Prados
Journal:  Neuro Oncol       Date:  2010-07-08       Impact factor: 12.300

5.  Epithelial Growth Factor Receptor Inhibitors for treatment of recurrent or progressive high grade glioma: an exploratory study.

Authors:  M Preusser; E Gelpi; A Rottenfusser; K Dieckmann; G Widhalm; W Dietrich; A Bertalanffy; D Prayer; J A Hainfellner; Christine Marosi
Journal:  J Neurooncol       Date:  2008-05-06       Impact factor: 4.130

6.  Phase I and pharmacokinetic studies of erlotinib administered concurrently with radiotherapy for children, adolescents, and young adults with high-grade glioma.

Authors:  Alberto Broniscer; Suzanne J Baker; Clinton F Stewart; Thomas E Merchant; Fred H Laningham; Paula Schaiquevich; Mehmet Kocak; E Brannon Morris; Raelene Endersby; David W Ellison; Amar Gajjar
Journal:  Clin Cancer Res       Date:  2009-01-15       Impact factor: 12.531

Review 7.  Pharmacotherapy for adults with tumors of the central nervous system.

Authors:  Nina F Schor
Journal:  Pharmacol Ther       Date:  2008-11-27       Impact factor: 12.310

8.  Erlotinib resistance in EGFR-amplified glioblastoma cells is associated with upregulation of EGFRvIII and PI3Kp110δ.

Authors:  Alexander Schulte; Katrin Liffers; Annegret Kathagen; Sabine Riethdorf; Svenja Zapf; Adrian Merlo; Katharina Kolbe; Manfred Westphal; Katrin Lamszus
Journal:  Neuro Oncol       Date:  2013-07-21       Impact factor: 12.300

9.  Randomized phase II trial of erlotinib versus temozolomide or carmustine in recurrent glioblastoma: EORTC brain tumor group study 26034.

Authors:  Martin J van den Bent; Alba A Brandes; Roy Rampling; Mathilde C M Kouwenhoven; Johan M Kros; Antoine F Carpentier; Paul M Clement; Marc Frenay; Mario Campone; Jean-Francois Baurain; Jean-Paul Armand; Martin J B Taphoorn; Alicia Tosoni; Heidemarie Kletzl; Barbara Klughammer; Denis Lacombe; Thierry Gorlia
Journal:  J Clin Oncol       Date:  2009-02-09       Impact factor: 44.544

10.  The drug-resistance to gefitinib in PTEN low expression cancer cells is reversed by irradiation in vitro.

Authors:  Hong-Qing Zhuang; Jun Wang; Zhi-Yong Yuan; Lu-Jun Zhao; Ping Wang; Chang-Li Wang
Journal:  J Exp Clin Cancer Res       Date:  2009-09-01
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