University of North Carolina Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, US.
Sidney Kimmel Cancer Center, Thomas Jefferson University Hospital, Philadelphia, PA, US.
Pharmacogenomics J. 2024 Jul 12;24(4):22. doi: 10.1038/s41397-024-00342-1.
Bevacizumab-induced hypertension poses a therapeutic challenge and identifying biomarkers for hypertension can enhance therapy safety. Lower plasma levels of VEGF-A, angiopoietin-2, and rs6770663 in KCNAB1 were previously associated with increased risk of bevacizumab-induced hypertension. This study investigated whether these factors independently contribute to grade 2-3 bevacizumab-induced hypertension risk in 277 cancer patients (CALGB/Alliance 90401). Multivariable analyses assessed the independent association of each factor and hypertension. Likelihood ratio test (LRT) evaluated the explanatory significance of combining protein levels and rs6770663 in predicting hypertension. Boostrap was employed to assess the mediation effect of protein levels on the rs6770663 association with hypertension. Lower protein levels and rs6770663 were independently associated with increased hypertension risk. Adding rs6770663 to protein levels improved the prediction of hypertension (LRT p = 0.0002), with no mediation effect observed. Protein levels of VEGF-A, angiopoietin-2 and rs6770663 in KCNAB1 are independent risk factors and, when combined, may improve prediction of bevacizumab-induced hypertension. ClinicalTrials.gov Identifier: NCT00110214.
贝伐珠单抗引起的高血压带来了治疗挑战,寻找高血压的生物标志物可以提高治疗安全性。先前的研究表明,KCNAB1 中的 VEGF-A、血管生成素-2 和 rs6770663 血浆水平较低与贝伐珠单抗引起的高血压风险增加有关。本研究在 277 名癌症患者(CALGB/Alliance 90401)中探讨了这些因素是否独立导致 2-3 级贝伐珠单抗引起的高血压风险。多变量分析评估了每个因素与高血压的独立关联。似然比检验(LRT)评估了联合蛋白水平和 rs6770663 预测高血压的解释意义。采用自举法评估蛋白水平对 rs6770663 与高血压关联的中介效应。较低的蛋白水平和 rs6770663 与高血压风险增加独立相关。在蛋白水平中添加 rs6770663 可改善高血压的预测(LRT p = 0.0002),未观察到中介效应。KCNAB1 中的 VEGF-A、血管生成素-2 和 rs6770663 的蛋白水平是独立的危险因素,联合使用时可能会改善对贝伐珠单抗引起的高血压的预测。临床试验注册号:NCT00110214。