Purpose: Despite the wide use of antiangiogenic drugs in the clinical setting, predictive
biomarkers of response to these drugs are still unknown.Experimental Design: We applied whole-exome sequencing of matched germline and basal plasma cell-free
DNA samples (WES-
cfDNA) on a RAS/BRAF/PIK3CA wild-type metastatic
colorectal cancer patient with primary resistance to standard treatment regimens, including inhibitors to the
VEGF:VEGFR2 pathway. We performed extensive functional experiments, including ectopic expression of VEGFR2 mutants in different cell lines,
kinase and drug sensitivity assays, and cell- and patient-derived xenografts.Results: WES-
cfDNA yielded a 77% concordance rate with
tumor exome sequencing and enabled the identification of the KDR/VEGFR2 L840F clonal, somatic mutation as the cause of
therapy refractoriness in our patient. In addition, we found that 1% to 3% of samples from
cancer sequencing projects harbor KDR somatic mutations located in
protein residues frequently mutated in other
cancer-relevant
kinases, such as EGFR, ABL1, and ALK. Our in vitro and in vivo functional assays confirmed that L840F causes strong resistance to antiangiogenic drugs, whereas the KDR hot-spot mutant R1032Q confers sensitivity to strong VEGFR2 inhibitors. Moreover, we showed that the D717V, G800D, G800R, L840F, G843D, S925F, R1022Q, R1032Q, and S1100F VEGFR2 mutants promote
tumor growth in mice.Conclusions: Our study supports WES-
cfDNA as a powerful platform for portraying the somatic mutation landscape of
cancer and discovery of new resistance mechanisms to
cancer therapies. Importantly, we discovered that VEGFR2 is somatically mutated across
tumor types and that VEGFR2 mutants can be oncogenic and control sensitivity/resistance to antiangiogenic drugs. Clin
Cancer Res; 24(15); 3550-9. ©2018 AACR.