Jubb Adrian M, Oates Adam J, Holden Scott, Koeppen Hartmut
Academic Unit of Pathology, Leeds Institute for Molecular Medicine, University of Leeds, UK.
Nat Rev Cancer. 2006 Aug;6(8):626-35. doi: 10.1038/nrc1946. Epub 2006 Jul 13.
A high probability of benefit is desirable to justify the choice of anti-angiogenic therapy from an ever-expanding list of expensive new anticancer agents. However, biomarkers of response to cytotoxic agents are not optimal for predicting benefit from anti-angiogenic drugs. This discussion will focus on both preclinical and clinical research to identify biomarkers for anti-angiogenic therapies that can inform dosing, early clinical benefit, initial drug choice, emerging resistance and second-line treatments.
为了从不断增加的昂贵新型抗癌药物清单中合理选择抗血管生成疗法,需要有较高的获益可能性。然而,细胞毒性药物的反应生物标志物并非预测抗血管生成药物获益的最佳指标。本讨论将聚焦于临床前和临床研究,以确定抗血管生成疗法的生物标志物,这些生物标志物可用于指导给药、早期临床获益、初始药物选择、新出现的耐药性及二线治疗。