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Clinical activity of the EGFR tyrosine kinase inhibitor osimertinib in EGFR -mutant glioblastoma
by
O’Rourke, Donald M
, Morrissette, Jennifer JD
, Nasrallah, MacLean P
, Salinas, Ryan D
, Bagley, Stephen J
, Desai, Arati S
, Ming, Gou-li
, Saxena, Deeksha
, Dorsey, Jay F
, Makhlin, Igor
, Zhang, Daniel
, Jacob, Fadi
, Brem, Steven
, Song, Hongjun
, Binder, Zev A
in
Acrylamides - therapeutic use
/ Adult
/ Aniline Compounds - therapeutic use
/ Binding sites
/ Blood-brain barrier
/ Brain cancer
/ Brain Neoplasms - drug therapy
/ Brain Neoplasms - enzymology
/ Brain Neoplasms - genetics
/ Brain Neoplasms - pathology
/ Case Report
/ EGFR
/ ErbB Receptors - antagonists & inhibitors
/ ErbB Receptors - genetics
/ Female
/ GBM
/ glioblastoma
/ Glioblastoma - drug therapy
/ Glioblastoma - enzymology
/ Glioblastoma - genetics
/ Glioblastoma - pathology
/ Histopathology
/ Humans
/ Kinases
/ Laboratories
/ Lung cancer
/ Magnetic resonance imaging
/ Metastasis
/ Mutation
/ osimertinib
/ Polymerase chain reaction
/ precision oncology
/ Prognosis
/ Protein Kinase Inhibitors - therapeutic use
/ Regulatory approval
/ Surgery
/ Tumors
/ tyrosine kinase inhibitor
2019
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Clinical activity of the EGFR tyrosine kinase inhibitor osimertinib in EGFR -mutant glioblastoma
by
O’Rourke, Donald M
, Morrissette, Jennifer JD
, Nasrallah, MacLean P
, Salinas, Ryan D
, Bagley, Stephen J
, Desai, Arati S
, Ming, Gou-li
, Saxena, Deeksha
, Dorsey, Jay F
, Makhlin, Igor
, Zhang, Daniel
, Jacob, Fadi
, Brem, Steven
, Song, Hongjun
, Binder, Zev A
in
Acrylamides - therapeutic use
/ Adult
/ Aniline Compounds - therapeutic use
/ Binding sites
/ Blood-brain barrier
/ Brain cancer
/ Brain Neoplasms - drug therapy
/ Brain Neoplasms - enzymology
/ Brain Neoplasms - genetics
/ Brain Neoplasms - pathology
/ Case Report
/ EGFR
/ ErbB Receptors - antagonists & inhibitors
/ ErbB Receptors - genetics
/ Female
/ GBM
/ glioblastoma
/ Glioblastoma - drug therapy
/ Glioblastoma - enzymology
/ Glioblastoma - genetics
/ Glioblastoma - pathology
/ Histopathology
/ Humans
/ Kinases
/ Laboratories
/ Lung cancer
/ Magnetic resonance imaging
/ Metastasis
/ Mutation
/ osimertinib
/ Polymerase chain reaction
/ precision oncology
/ Prognosis
/ Protein Kinase Inhibitors - therapeutic use
/ Regulatory approval
/ Surgery
/ Tumors
/ tyrosine kinase inhibitor
2019
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Clinical activity of the EGFR tyrosine kinase inhibitor osimertinib in EGFR -mutant glioblastoma
by
O’Rourke, Donald M
, Morrissette, Jennifer JD
, Nasrallah, MacLean P
, Salinas, Ryan D
, Bagley, Stephen J
, Desai, Arati S
, Ming, Gou-li
, Saxena, Deeksha
, Dorsey, Jay F
, Makhlin, Igor
, Zhang, Daniel
, Jacob, Fadi
, Brem, Steven
, Song, Hongjun
, Binder, Zev A
in
Acrylamides - therapeutic use
/ Adult
/ Aniline Compounds - therapeutic use
/ Binding sites
/ Blood-brain barrier
/ Brain cancer
/ Brain Neoplasms - drug therapy
/ Brain Neoplasms - enzymology
/ Brain Neoplasms - genetics
/ Brain Neoplasms - pathology
/ Case Report
/ EGFR
/ ErbB Receptors - antagonists & inhibitors
/ ErbB Receptors - genetics
/ Female
/ GBM
/ glioblastoma
/ Glioblastoma - drug therapy
/ Glioblastoma - enzymology
/ Glioblastoma - genetics
/ Glioblastoma - pathology
/ Histopathology
/ Humans
/ Kinases
/ Laboratories
/ Lung cancer
/ Magnetic resonance imaging
/ Metastasis
/ Mutation
/ osimertinib
/ Polymerase chain reaction
/ precision oncology
/ Prognosis
/ Protein Kinase Inhibitors - therapeutic use
/ Regulatory approval
/ Surgery
/ Tumors
/ tyrosine kinase inhibitor
2019
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Clinical activity of the EGFR tyrosine kinase inhibitor osimertinib in EGFR -mutant glioblastoma
Journal Article
Clinical activity of the EGFR tyrosine kinase inhibitor osimertinib in EGFR -mutant glioblastoma
2019
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Overview
Glioblastoma (GBM) is the most common primary malignant brain tumor in adults and carries a dismal prognosis. The
gene is among the most commonly deranged genes in GBM and thus an important therapeutic target. We report the case of a young female with heavily pretreated
-mutated GBM, for whom we initiated osimertinib, an oral, third-generation tyrosine kinase inhibitor that irreversibly inhibits EGFR and has significant brain penetration. We then review some of the main challenges in targeting EGFR, including lack of central nervous system penetration with most tyrosine kinase inhibitors, molecular heterogeneity of GBM and the need for enhanced specificity for the
mutations relevant in GBM.
Publisher
Future Medicine Ltd,Taylor & Francis Group
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