Department of Medical Oncology, Necmettin Erbakan University School of Medicine, Konya, 42080, Turkey.
Eur J Clin Pharmacol. 2024 Jun;80(6):941-947. doi: 10.1007/s00228-024-03668-8. Epub 2024 Mar 13.
Vascular endothelial growth factor (VEGF) inhibition is one of the cornerstones of treatment in the treatment of metastatic renal cell carcinoma (mRCC). Since RCC is a disease of advanced age and hypertension as a side effect of VEGF receptor inhibitors, beta-blocker use is common in these patients. We aimed to compare the treatment efficacy and survival results in case of concomitant use of these two drugs due to the inhibition of VEGF in beta-blockers.
A total of 121 patients with a diagnosis of mRCC who used sunitinib or pazopanib in first-line therapy were included in the study. These patients were divided into two groups as those using concomitant beta-blockers and those not using them.
The median overall survival (mOS) of the patient using sunitinib or pazopanib and concomitant beta-blocker was 47 (95% CI 29.0-65.0) months, and the mOS of those not using concomitant beta-blocker was 18 (95% CI 8.9-27.1) months (p < 0.001). The median progression-free survival (mPFS) of the patients using sunitinib or pazopanib and concomitant beta-blocker was 20.4 (95% CI 4.5-40.1) months, and the mPFS of those not using it was 11.4 (95% CI 5.9-16.9) months (p = 0.042). Concomitant beta-blocker use was found to be a good prognostic factor for OS in the multivariate analysis (p = 0.029). In the multivariate analysis, concomitant beta-blocker use had a trend towards statistical significance for PFS (p = 0.062).
Concomitant use of betablockers with sunitinib or pazopanib is associated with longer overall survial and progression free survival.
血管内皮生长因子(VEGF)抑制是转移性肾细胞癌(mRCC)治疗的基石之一。由于 RCC 是一种老年疾病,并且 VEGF 受体抑制剂会产生高血压副作用,因此这些患者中β受体阻滞剂的使用很常见。我们旨在比较由于 VEGF 在β受体阻滞剂中的抑制作用而同时使用这两种药物的治疗效果和生存结果。
共有 121 名接受舒尼替尼或帕唑帕尼一线治疗的 mRCC 患者纳入本研究。这些患者分为同时使用β受体阻滞剂和不使用β受体阻滞剂两组。
同时使用舒尼替尼或帕唑帕尼和β受体阻滞剂的患者中位总生存期(mOS)为 47 个月(95%CI 29.0-65.0),而不使用β受体阻滞剂的患者 mOS 为 18 个月(95%CI 8.9-27.1)(p<0.001)。同时使用舒尼替尼或帕唑帕尼和β受体阻滞剂的患者中位无进展生存期(mPFS)为 20.4 个月(95%CI 4.5-40.1),而不使用β受体阻滞剂的患者 mPFS 为 11.4 个月(95%CI 5.9-16.9)(p=0.042)。多变量分析显示,同时使用β受体阻滞剂是 OS 的良好预后因素(p=0.029)。多变量分析显示,同时使用β受体阻滞剂对 PFS 有统计学意义的趋势(p=0.062)。
舒尼替尼或帕唑帕尼与β受体阻滞剂同时使用与总生存期和无进展生存期延长相关。