Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan;
Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Anticancer Res. 2024 Feb;44(2):781-786. doi: 10.21873/anticanres.16869.
BACKGROUND/AIM: Although the adverse events (AEs) of drugs, such as sunitinib and axitinib, have been shown to predict treatment responses, evidence to support cabozantinib-induced AEs as predictors of responses to treatment for metastatic renal cell carcinoma (mRCC) is limited. Therefore, we herein investigated the relationship between AE profiles and progression-free survival (PFS) in patients receiving cabozantinib for previously treated mRCC.
The present study retrospectively analyzed 40 patients receiving cabozantinib for previously treated mRCC between July 2020 and August 2022. PFS was estimated using the Kaplan-Meier method and the impact of several parameters, including cabozantinib-induced AEs, on PFS was investigated by a Cox proportional regression analysis.
The median observation period was 15 (2-29) months, during which time 31 patients (77.5%) progressed, with median PFS of 11 months. Thirty-nine patients (97.5%) developed at least one AE. Liver toxicity occurred in 16 patients (40.0%) and hand-foot syndrome, hypertension, and diarrhea in 14 each (17.5%). Only hypertension correlated with longer PFS. A multivariate analysis identified hypertension as an independent prognostic factor for PFS (p=0.049).
These results suggest the potential of treatment-induced hypertension as a significant predictor of prolonged PFS in patients receiving cabozantinib for mRCC.
背景/目的:尽管舒尼替尼和阿昔替尼等药物的不良反应 (AE) 已被证明可预测治疗反应,但支持卡博替尼引起的 AE 作为转移性肾细胞癌 (mRCC) 治疗反应预测因子的证据有限。因此,我们在此研究了卡博替尼治疗既往治疗过的 mRCC 患者的 AE 谱与无进展生存期 (PFS) 之间的关系。
本研究回顾性分析了 2020 年 7 月至 2022 年 8 月期间接受卡博替尼治疗的 40 例既往治疗过的 mRCC 患者。使用 Kaplan-Meier 法估计 PFS,并通过 Cox 比例回归分析研究包括卡博替尼诱导的 AE 在内的几个参数对 PFS 的影响。
中位观察期为 15 个月(2-29 个月),期间 31 例患者(77.5%)进展,中位 PFS 为 11 个月。39 例患者(97.5%)至少发生 1 种 AE。16 例患者(40.0%)发生肝毒性,手足综合征、高血压和腹泻各 14 例(17.5%)。只有高血压与较长的 PFS 相关。多变量分析确定高血压是 PFS 的独立预后因素(p=0.049)。
这些结果表明,治疗引起的高血压可能是卡博替尼治疗 mRCC 患者 PFS 延长的一个重要预测因素。