Therapeutic options targeting angiogenesis in nonsmall cell lung cancer
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作者:
Crino, Lucio
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Azienda Osped Perugia, Santa Maria Misericordia Hosp, Div Med Oncol, Perugia, ItalyAzienda Osped Perugia, Santa Maria Misericordia Hosp, Div Med Oncol, Perugia, Italy
Crino, Lucio
[1
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Metro, Giulio
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Azienda Osped Perugia, Santa Maria Misericordia Hosp, Div Med Oncol, Perugia, ItalyAzienda Osped Perugia, Santa Maria Misericordia Hosp, Div Med Oncol, Perugia, Italy
Metro, Giulio
[1
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机构:
[1] Azienda Osped Perugia, Santa Maria Misericordia Hosp, Div Med Oncol, Perugia, Italy
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.
机构:
Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle Canc Care Alliance, 825 Eastlake Ave East, Seattle, WA 98109 USAUniv Washington, Fred Hutchinson Canc Res Ctr, Seattle Canc Care Alliance, 825 Eastlake Ave East, Seattle, WA 98109 USA
机构:
Univ Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, GreeceUniv Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, Greece
Stratigos, Michalis
Matikas, Alexios
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Univ Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, Greece
HORG, Athens, GreeceUniv Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, Greece
Matikas, Alexios
Voutsina, Alexandra
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机构:
Univ Crete, Sch Med, Lab Translat Oncol, Iraklion, Crete, GreeceUniv Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, Greece
Voutsina, Alexandra
Mavroudis, Dimitrios
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Univ Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, Greece
Univ Crete, Sch Med, Lab Translat Oncol, Iraklion, Crete, GreeceUniv Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, Greece
Mavroudis, Dimitrios
Georgoulias, Vassilis
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HORG, Athens, Greece
Univ Crete, Sch Med, Lab Translat Oncol, Iraklion, Crete, GreeceUniv Gen Hosp Heraklion, Dept Med Oncol, POB 1352, Iraklion 71110, Crete, Greece