Epidermal growth factor receptor (EGFR)-targeted therapies in mesothelioma

被引:22
|
作者
Chia, Puey Ling [1 ,2 ,3 ]
Scott, Andrew M. [2 ,3 ,4 ,5 ,6 ]
John, Thomas [1 ,3 ,4 ,7 ]
机构
[1] Austin Hlth, Dept Med Oncol, Melbourne, Vic, Australia
[2] Olivia Newton John Canc Res Inst, Tumour Targeting Lab, Melbourne, Vic, Australia
[3] Univ Melbourne, Fac Med, Melbourne, Vic, Australia
[4] La Trobe Univ, Sch Canc Med, Melbourne, Vic, Australia
[5] Austin Hlth, Dept Mol Imaging & Therapy, Melbourne, Vic, Australia
[6] Univ Melbourne, Melbourne, Vic, Australia
[7] Olivia Newton John Canc Res Inst, Canc Immunobiol Lab, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
Epidermal growth factor receptor (EGFR); EGFR overexpression; malignant mesothelioma; targeted therapies; MALIGNANT PLEURAL MESOTHELIOMA; CELL LUNG-CANCER; TYROSINE KINASE DOMAIN; GENE COPY NUMBER; OPEN-LABEL; PHASE-III; PROTEIN EXPRESSION; ACTIVATING MUTATIONS; EGFR EXPRESSION; ANTIBODY;
D O I
10.1080/17425247.2019.1598374
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Malignant mesothelioma (MM) is an aggressive malignancy arising from the mesothelial cells lining the pleura and other serosal membranes. It is associated with an extremely poor prognosis and has limited therapeutic options. Areas covered: Epidermal growth factor receptor (EGFR) is known to be highly overexpressed in mesothelioma with reported EGFR overexpression between 44 to 97%. Given this, several anti-EGFR agents have been trialed in mesothelioma. In this review, we provide an overview of the current available data on anti-EGFR therapies in MM and future directions of investigation with these targeted agents in MM. Expert opinion: While many anti-EGFR therapies have failed to show significant efficacy in the management of MM, the pathway is biologically active and its abrogation preclinically points toward it being a valid target. Toward targeting the pathway, many novel EGFR-based therapies are still being investigated. Current ongoing research of interest in MM include EGFR-targeted nanotechnology approach for drug delivery, antibodies targeting the extracellular EGFR and potentially anti-EGFR antibody drug conjugates.
引用
收藏
页码:441 / 451
页数:11
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