Division of Pharmacotherapy and Experimental Therapeutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Pharmacogenomics J. 2022 Feb;22(1):82-88. doi: 10.1038/s41397-021-00261-5. Epub 2021 Nov 13.
No biomarkers are available to predict patients at risk of developing hypertension induced by VEGF-pathway inhibitors. This study aimed to identify predictive biomarkers of hypertension induced by these drugs using a discovery-replication approach. The discovery set included 140 sorafenib-treated patients (TARGET study) genotyped for 973 SNPs in 56 genes. The most statistically significant SNPs associated with grade ≥2 hypertension were tested for association with grade ≥2 hypertension in the replication set of a GWAS of 1039 bevacizumab-treated patients from four clinical trials (CALGB/Alliance). In the discovery set, rs444904 (G > A) in PIK3R5 was associated with an increased risk of sorafenib-induced hypertension (p = 0.006, OR = 3.88 95% CI 1.54-9.81). In the replication set, rs427554 (G > A) in PIK3R5 (in complete linkage disequilibrium with rs444904) was associated with an increased risk of bevacizumab-induced hypertension (p = 0.008, OR = 1.39, 95% CI 1.09-1.78). This study identified a predictive marker of drug-induced hypertension that should be evaluated for other VEGF-pathway inhibitors.ClinicalTrials.gov Identifier:NCT00073307 (TARGET).
目前尚无生物标志物可预测接受 VEGF 通路抑制剂治疗的患者发生高血压的风险。本研究旨在采用发现-复制方法,鉴定这些药物引起的高血压的预测性生物标志物。发现组纳入了 140 例接受索拉非尼治疗的患者(TARGET 研究),这些患者在 56 个基因中的 973 个 SNP 进行了基因分型。与 2 级及以上高血压相关的最显著的 SNP ,在来自四项临床试验的 1039 例贝伐珠单抗治疗患者的 GWAS 复制组(CALGB/Alliance)中,进行了与 2 级及以上高血压相关的关联性检验。在发现组中,PIK3R5 中的 rs444904(G > A)与索拉非尼引起的高血压风险增加相关(p = 0.006,OR = 3.88,95%CI 1.54-9.81)。在复制组中,PIK3R5 中的 rs427554(G > A)(与 rs444904 完全连锁不平衡)与贝伐珠单抗引起的高血压风险增加相关(p = 0.008,OR = 1.39,95%CI 1.09-1.78)。本研究鉴定了药物引起的高血压的预测性标志物,应该在其他 VEGF 通路抑制剂中进行评估。临床试验.gov 标识符:NCT00073307(TARGET)。