A DAGANATOS ÉRHÁLÓZAT MINT TERÁPIÁS CÉLPONT NEM KISSEJTES TÜDŐRÁKBAN

2008 
Bar a sebeszi reszekcio, a platina-alapu kemoterapias kombinaciok es a sugarterapia javitott ak a tulelesi eredmenyeken, a nem kissejtes tudőrak (NSCLC) tulelesenek novekedesi gorbeje plato fazisahoz erkezett . Az uj terapias lehetősegek koze tartoznak a molekularis celzott terapiak, ezeken belul a tumorok erhalozatara hato szerek. Jelenleg a bevacizumab – mely egy a vaszkularis endothelialis novekedesi faktor (VEGF) elleni rekombinans, monoklonalis antitest – a klinikai fejlesztesek legelőrehaladott abb stadiumban levő gyogyszere. Ugyanakkor mas celzott erellenes szerek is – beleertve a VDA-kat (vascular disrupting agents) es kulonfele kis molekulaju tirozinkinaz-inhibitorokat – remenykeltők voltak a preklinikai es klinikai vizsgalatokban. Jelen kozlemenyunkben att ekintjuk az NSCLC-ben onmagukban vagy kemoterapiaval kombinaltan alkalmazhato antivaszkularis terapias strategiakat. Magyar Onkologia 52: 247–259, 2008 Kulcsszavak: angiogenezis, tudőrak Despite developments in conventional (chemo)radiotherapy and surgery, survival of non-small cell lung cancer (NSCLC) patients remains poor. Treatments with targeted molecular drugs off er novel therapeutic strategies. Bevacizumab, a recombinant anti-vascular endothelial growth factor (VEGF) antibody, is the antiangiogenic drug at the most advanced stage of development in the therapy of NSCLC. However, a number of questions and future challenges relating to the use of bevacizumab in NSCLC remain. Furthermore, novel agents targeting the pre-existing NSCLC vasculature (i.e. vascular disrupting agents, VDAs) or multiple tyrosine kinase inhibitors have emerged as unique drug classes delivering promising results in several preclinical and clinical studies. Herein, we review the most recent data using these novel targeted agents either alone or in combination with chemotherapy in NSCLC. Dome B, Magyar M. Tumor vasculature as a therapeutic target in non-small cell lung cancer. Hungarian Oncology 52: 247–259, 2008
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