作者
AJ Weickhardt, DS Williams, CK Lee, F Chionh, J Simes, C Murone, K Wilson, MM Parry, K Asadi, AM Scott, CJA Punt, ID Nagtegaal, TJ Price, JM Mariadason, NC Tebbutt
发表日期
2015/6
期刊
British journal of cancer
卷号
113
期号
1
页码范围
37-45
出版商
Nature Publishing Group
简介
Background:
Bevacizumab prolongs progression-free survival (PFS) in patients with metastatic colorectal cancer. We analysed the protein expression levels of vascular endothelial growth factor (VEGF) ligands and receptors to determine their prognostic and predictive effects.
Methods:
We graded expression of VEGF-A, VEGF-B, VEGF-C, VEGF-D, VEGF-R1, and VEGF-R2 to assess whether overexpression predicted bevacizumab resistance in samples from 268 of 471 patients randomised to capecitabine (C), capecitabine and bevacizumab (CB), or CB and mitomycin (CBM) in the MAX trial and extended the analysis to the CAIRO-2 population.
Results:
Patients with low expression of VEGF-D (0, 1+) benefited from bevacizumab treatment (PFS hazard ratio (HR)(C vs CB+ CBM), 0.21; 95% CI, 0.08–0.55; overall survival (OS) HR, 0.35; 95% CI, 0.13–0.90). Patients with higher VEGF-D expression received less benefit …
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