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转移性肾细胞癌患者接受血管内皮生长因子受体酪氨酸激酶抑制剂治疗的剂量强度。

Dose Intensity in Real-World Patients With Metastatic Renal Cell Carcinoma Taking Vascular Endothelial Growth Factor Receptor Tyrosine Kinase Inhibitors.

机构信息

School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.

Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.

出版信息

Clin Genitourin Cancer. 2023 Jun;21(3):357-365. doi: 10.1016/j.clgc.2023.02.007. Epub 2023 Feb 16.

Abstract

BACKGROUND

Tyrosine kinase inhibitors (TKIs) that target the vascular endothelial growth factor receptor (VEGFR) are oral therapies used to treat metastatic renal cell carcinoma (mRCC). VEGFR TKI treatment is often complicated by dose-limiting adverse events (AE). We sought to describe dose intensity and clinical outcomes in a real-world cohort of patients treated with VEGFR TKIs to better characterize dosing patterns and toxicity management compared with previously reported clinical trials.

MATERIALS AND METHODS

We conducted a retrospective chart review of sequential patients with mRCC treated with VEGFR TKIs at 1 academic medical center from 2014 to 2021.

RESULTS

139 patients (75% male, 75% white, median age 63 years) were treated with 185 VEGFR TKIs in our real-world cohort. Per International Metastatic RCC Database Consortium criteria, 24% had good risk, 54% intermediate risk, and 22% poor risk mRCC. With their first VEGFR TKI, median relative dose intensity (RDI) was 79%. 52% of patients required a dose reduction, 11% discontinued treatment due to AEs, 15% visited the ED, and 13% were hospitalized for treatment-related adverse events. Cabozantinib had the highest rate of dose reductions (72%) but a low rate of discontinuation (7%). Real-world patients consistently had lower RDI than reported clinical trials with more frequent dose reductions, fewer drug discontinuations, shorter progression-free survival, and shorter overall survival.

CONCLUSION

Real-world patients were less able to tolerate VEGFR TKIs compared to patients treated on clinical trials. Low real-world RDI, high dose reductions, and low overall discontinuation rates can inform patient counseling prior to treatment initiation and during therapy.

摘要

背景

针对血管内皮生长因子受体 (VEGFR) 的酪氨酸激酶抑制剂 (TKI) 是用于治疗转移性肾细胞癌 (mRCC) 的口服疗法。VEGFR TKI 治疗常因剂量限制不良事件 (AE) 而变得复杂。我们旨在描述在接受 VEGFR TKI 治疗的真实世界患者队列中的剂量强度和临床结局,以便与之前报道的临床试验相比更好地描述剂量模式和毒性管理。

材料和方法

我们对 2014 年至 2021 年期间在一家学术医疗中心接受 VEGFR TKI 治疗的 mRCC 连续患者进行了回顾性图表审查。

结果

在我们的真实世界队列中,139 名患者(75%为男性,75%为白人,中位年龄 63 岁)接受了 185 种 VEGFR TKI 治疗。根据国际转移性肾细胞癌数据库联盟标准,24%的患者为低危,54%为中危,22%为高危 mRCC。在他们的第一次 VEGFR TKI 治疗中,中位相对剂量强度 (RDI) 为 79%。52%的患者需要减少剂量,11%因 AE 而停止治疗,15%去急诊室就诊,13%因治疗相关不良事件住院。卡博替尼的剂量减少率最高(72%),但停药率最低(7%)。真实世界的患者与接受临床试验的患者相比,能够耐受 VEGFR TKI 的能力较低。较低的真实世界 RDI、较高的剂量减少率、较低的总体停药率可以为治疗前和治疗期间的患者咨询提供信息。

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