Genetic markers of bevacizumab-induced hypertension

作者：Lambrechts Diether^*; Moisse Matthieu; Delmar Paul; Miles David W; Leighl Natasha; Escudier Bernard; Van Cutsem Eric; Bansal Aruna T; Carmeliet Peter; Scherer Stefan J; de Haas Sanne; Pallaud Celine

来源：Angiogenesis, 2014, 17(3): 685-694.

DOI：10.1007/s10456-014-9424-7

• Anti-angiogenesis
• Bevacizumab
• Hypertension
• Single nucleotide polymorphism
• Predictive biomarker

There are currently no validated biomarkers predicting bevacizumab treatment outcome or toxicity. We combined biomarker data from six phase III trials of bevacizumab to assess whether genetic variation in vascular endothelial growth factor-A (VEGF-A) pathway or hypertension-related genes are associated with bevacizumab-induced hypertension.
Germline DNA was available from 1,631 patients receiving bevacizumab-containing therapy for advanced solid tumors. Overall, 194 white patients had grade 1-4 bevacizumab-induced hypertension. In total, 236 single nucleotide polymorphisms (SNPs) located in VEGF-A, VEGF-A receptors (FLT1 and KDR), and other genes were selected using a SNP tagging approach and genotyped. A logistic regression on individual patient data was performed after adjustment for cancer type and five other covariates.
Ten SNPs were associated with bevacizumab-induced hypertension (P a parts per thousand currency sign 0.05), but none surpassed the threshold adjusted for multiple testing (P < 0.0002). The most significant VEGF-A pathway SNP was rs1680695 in EGLN3 [allelic odds ratio (OR) 1.50 [95 % confidence interval (Cl) 1.09-2.07], P = 0.012]. Two additional SNPs, rs4444903 in EGF and rs2305949 in KDR, were associated with hypertension (allelic OR 1.57 [95 % CI 1.17-2.11], P = 0.0025; allelic OR 0.62 [95 % CI 0.42-0.93], P = 0.020, respectively) and closely linked to nearby functional variants. Consistent with previous reports, rs11064560 in WNK1 was also associated with bevacizumab-induced hypertension (OR 1.41 [95 % CI 1.04-1.92], P = 0.028).
The genes described in this large genetic analysis using pooled datasets warrant further functional investigation regarding their role in mediating bevacizumab-induced hypertension.

• 出版日期2014-7
• 单位KU Leuven