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一项评估血管内皮生长因子受体(VEGFR)激酶抑制剂凡德他尼与 mTOR 抑制剂依维莫司联合用于治疗晚期实体瘤患者的 I 期临床研究。

A phase I study of the VEGFR kinase inhibitor vatalanib in combination with the mTOR inhibitor, everolimus, in patients with advanced solid tumors.

机构信息

Mayo Clinic, 200 First St. SW, Rochester, MN, 55905, USA.

Roswell Park Cancer Institute, Buffalo, NY, 14263, USA.

出版信息

Invest New Drugs. 2020 Dec;38(6):1755-1762. doi: 10.1007/s10637-020-00936-z. Epub 2020 Apr 24.

Abstract

Purpose Combining small-molecule inhibitors of different targets was shown to be synergistic in preclinical studies. Testing this concept in clinical trials is, however, daunting due to challenges in toxicity management and efficacy assessment. This study attempted to evaluate the safety and efficacy of vatalanib plus everolimus in patients with advanced solid tumors and explore the utility of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) studies as a predictive biomarker. Patients and Methods This single-center, phase I trial containing 70 evaluable patients consisted of a dose escalation proportion based on the traditional "3 + 3" design (cohort IA and IB) and a dose expansion proportion (cohort IIA and IIB). Toxicity was evaluated using the Common Terminology Criteria of Adverse Events. Antitumor activity was assessed using the Modified Response Evaluation Criteria in Solid Tumors. Results The maximum tolerated doses were determined to be vatalanib 1250 mg once daily or 750 mg twice daily in combination with everolimus 10 mg once daily. No treatment-related death occurred. The most common toxicities were hypertriglyceridemia, hypercholesterolemia, fatigue, vomiting, nausea and diarrhea. There was no complete response. Nine patients (12.9%) had partial response (PR) and 41 (58.6%) had stable disease (SD). Significant antitumor activity was observed in neuroendocrine tumors with a disease-control rate (PR + SD) of 66.7% and other tumor types including renal cancer, melanoma, and non-small-cell lung cancer. Conclusions The combination of vatalanib and everolimus demonstrated reasonable toxicity and clinical activity. Future studies combining targeted therapies and incorporating biomarker analysis are warranted based on this phase I trial.

摘要

目的

在临床前研究中,联合使用针对不同靶点的小分子抑制剂已被证明具有协同作用。然而,由于毒性管理和疗效评估方面的挑战,在临床试验中测试这一概念具有很大的挑战性。本研究旨在评估伐他拉尼联合依维莫司在晚期实体瘤患者中的安全性和疗效,并探索动态对比增强磁共振成像(DCE-MRI)研究作为预测生物标志物的效用。

方法

本研究为单中心、70 例可评估患者的 I 期临床试验,包含基于传统“3+3”设计的剂量递增部分(IA 队列和 IB 队列)和剂量扩展部分(IIA 队列和 IIB 队列)。采用不良事件常用术语标准评估毒性。采用实体瘤改良疗效评价标准评估抗肿瘤活性。

结果

确定伐他拉尼 1250mg 每日 1 次或 750mg 每日 2 次联合依维莫司 10mg 每日 1 次为最大耐受剂量。未发生与治疗相关的死亡。最常见的毒性反应为高甘油三酯血症、高胆固醇血症、疲劳、呕吐、恶心和腹泻。无完全缓解。9 例(12.9%)患者部分缓解(PR),41 例(58.6%)患者疾病稳定(SD)。神经内分泌肿瘤的疾病控制率(PR+SD)为 66.7%,其他肿瘤类型(包括肾细胞癌、黑色素瘤和非小细胞肺癌)也观察到显著的抗肿瘤活性。

结论

伐他拉尼联合依维莫司具有合理的毒性和临床活性。基于该 I 期试验,未来需要进行联合靶向治疗并纳入生物标志物分析的研究。

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