Therapeutic options targeting angiogenesis in nonsmall cell lung cancer

There is a major unmet medical need for effective and well-tolerated treatment options for patients with advanced nonsmall cell lung cancer (NSCLC), in both first-line and relapsed/refractory settings. Experimental evidence has validated signalling pathways that regulate tumour angiogenesis, includi...

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Main Authors: Lucio Crinò, Giulio Metro
Format: Article
Language:English
Published: European Respiratory Society 2014-03-01
Series:European Respiratory Review
Online Access:http://err.ersjournals.com/content/23/131/79.full.pdf+html
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spelling doaj-6f680c52730b4641b354767c75ebda902020-11-24T21:47:26ZengEuropean Respiratory SocietyEuropean Respiratory Review0905-91801600-06172014-03-0123131799110.1183/09059180.00008913 Therapeutic options targeting angiogenesis in nonsmall cell lung cancer Lucio Crinò Giulio MetroThere is a major unmet medical need for effective and well-tolerated treatment options for patients with advanced nonsmall cell lung cancer (NSCLC), in both first-line and relapsed/refractory settings. Experimental evidence has validated signalling pathways that regulate tumour angiogenesis, including the vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF) and fibroblast growth factor (FGF) pathways, as valid anti-cancer drug targets. However, to date, bevacizumab (an anti-VEGF monoclonal antibody) is the only antiangiogenic agent to be approved for the treatment of NSCLC. Many other agents, including antibodies, small-molecule tyrosine kinase inhibitors and vascular disrupting agents, have been assessed in phase III trials but have generally failed to demonstrate clinically meaningful benefits. This lack of success probably reflects the redundancy of proangiogenic pathways and the molecular and clinical heterogeneity of NSCLC. In this review we summarise recently completed and ongoing randomised clinical trials of emerging antiangiogenic agents in patients with NSCLC. We highlight recent promising data with agents that simultaneously inhibit multiple proangiogenic pathways, including the PDGF and FGF pathways, as well as the VEGF pathway. Finally, we discuss the outlook for antiangiogenic agents in NSCLC, emphasising the need for clinically validated prognostic and predictive biomarkers to identify patients most likely to respond to therapy. http://err.ersjournals.com/content/23/131/79.full.pdf+html
collection DOAJ
language English
format Article
sources DOAJ
author Lucio Crinò
Giulio Metro
spellingShingle Lucio Crinò
Giulio Metro
Therapeutic options targeting angiogenesis in nonsmall cell lung cancer
European Respiratory Review
author_facet Lucio Crinò
Giulio Metro
author_sort Lucio Crinò
title Therapeutic options targeting angiogenesis in nonsmall cell lung cancer
title_short Therapeutic options targeting angiogenesis in nonsmall cell lung cancer
title_full Therapeutic options targeting angiogenesis in nonsmall cell lung cancer
title_fullStr Therapeutic options targeting angiogenesis in nonsmall cell lung cancer
title_full_unstemmed Therapeutic options targeting angiogenesis in nonsmall cell lung cancer
title_sort therapeutic options targeting angiogenesis in nonsmall cell lung cancer
publisher European Respiratory Society
series European Respiratory Review
issn 0905-9180
1600-0617
publishDate 2014-03-01
description There is a major unmet medical need for effective and well-tolerated treatment options for patients with advanced nonsmall cell lung cancer (NSCLC), in both first-line and relapsed/refractory settings. Experimental evidence has validated signalling pathways that regulate tumour angiogenesis, including the vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF) and fibroblast growth factor (FGF) pathways, as valid anti-cancer drug targets. However, to date, bevacizumab (an anti-VEGF monoclonal antibody) is the only antiangiogenic agent to be approved for the treatment of NSCLC. Many other agents, including antibodies, small-molecule tyrosine kinase inhibitors and vascular disrupting agents, have been assessed in phase III trials but have generally failed to demonstrate clinically meaningful benefits. This lack of success probably reflects the redundancy of proangiogenic pathways and the molecular and clinical heterogeneity of NSCLC. In this review we summarise recently completed and ongoing randomised clinical trials of emerging antiangiogenic agents in patients with NSCLC. We highlight recent promising data with agents that simultaneously inhibit multiple proangiogenic pathways, including the PDGF and FGF pathways, as well as the VEGF pathway. Finally, we discuss the outlook for antiangiogenic agents in NSCLC, emphasising the need for clinically validated prognostic and predictive biomarkers to identify patients most likely to respond to therapy.
url http://err.ersjournals.com/content/23/131/79.full.pdf+html
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