Division of Urology, Shizuoka Cancer Center, Shizuoka, Japan.
Cancer Sci. 2013 Aug;104(8):1039-44. doi: 10.1111/cas.12197. Epub 2013 Jun 21.
Tivozanib is a potent and selective inhibitor of vascular endothelial growth factor receptor (VEGFR) tyrosine kinases. A previous clinical trial in the EU and USA indicated that tivozanib at the maximum tolerated dose of 1.5 mg/day showed an antitumor activity in patients with renal cell carcinoma. This Japanese phase I study was designed to determine the recommended phase II dose of tivozanib for Japanese patients; secondary objectives included pharmacokinetic/pharmacodynamic profiles and preliminary efficacy. Daily treatment with tivozanib in a 3-weeks-on/1-week-off cycle was examined in nine Japanese patients with advanced solid tumors in the 3 + 3 design (Level 1, 1.0 mg; Level 2, 1.5 mg). No dose-limiting toxicity was observed throughout the study, and the maximum tolerated dose was not reached. The most commonly observed drug-related adverse events were diarrhea, dysphonia, rash, thyroid stimulating hormone increase, and with severity grade ≥3, hand-foot skin reaction, hypertension, and proteinuria. Those adverse events were generally well-manageable and mostly resolved within the tolerability evaluation period. Serum exposure to tivozanib resulted in t1/2 of more than >60 h. Increase of plasma VEGF and decrease of plasma VEGFR-1 and VEGFR-2 were observed 1-3 weeks after tivozanib treatment. Although no complete or partial response was observed, long-term stable disease continuing more than 170 days was observed in three renal cell carcinoma patients who had failed prior VEGFR inhibitors. In conclusion, 1.5 mg/day of tivozanib in a 3-weeks-on/1-week-off setting was tolerable in Japanese patients, and was recommended for further clinical trials in the Japanese population. Clinical trial Registration No: JapicCTI-090854.
替沃扎尼布是一种强效和选择性的血管内皮生长因子受体(VEGFR)酪氨酸激酶抑制剂。一项在欧盟和美国进行的先前临床试验表明,替沃扎尼布在最大耐受剂量 1.5mg/天的情况下,在肾细胞癌患者中显示出抗肿瘤活性。这项日本 I 期研究旨在确定替沃扎尼布在日本患者中的推荐 II 期剂量;次要目标包括药代动力学/药效学特征和初步疗效。在 3 + 3 设计中(1.0mg 为水平 1,1.5mg 为水平 2),在 9 名患有晚期实体瘤的日本患者中,以 3 周给药/1 周停药的周期每日给予替沃扎尼布治疗。整个研究过程中未观察到剂量限制性毒性,也未达到最大耐受剂量。最常见的药物相关不良事件是腹泻、发声困难、皮疹、促甲状腺激素增加,以及严重程度≥3 级的手足皮肤反应、高血压和蛋白尿。这些不良事件通常易于管理,并且在可耐受评估期内大多得到解决。替沃扎尼布的血清暴露导致 t1/2 超过>60h。在替沃扎尼布治疗后 1-3 周观察到血浆 VEGF 增加和血浆 VEGFR-1 和 VEGFR-2 减少。虽然没有观察到完全或部分缓解,但在 3 名先前接受 VEGFR 抑制剂治疗失败的肾细胞癌患者中,观察到长期稳定疾病持续超过 170 天。总之,1.5mg/天的替沃扎尼布在 3 周给药/1 周停药方案中在日本患者中是可耐受的,并被推荐用于日本人群的进一步临床试验。临床试验注册号:JapicCTI-090854。