Department of Urology, Medical University of Vienna, Vienna, Austria.
Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Acta Oncol. 2022 Jan;61(1):52-57. doi: 10.1080/0284186X.2021.1995041. Epub 2021 Nov 4.
METEOR was a phase 3 trial (NCT01865747) of cabozantinib versus everolimus in adults with advanced or metastatic clear cell RCC previously treated with VEGF receptor (VEGFR) tyrosine kinase inhibitors (TKIs). This analysis of METEOR compared outcomes for patients recruited from European and non-European countries.
Adults with advanced/metastatic clear cell RCC who had received ≥ 1 prior VEGFR-TKI treatment were randomized 1:1 to receive cabozantinib or everolimus. Patients were categorized by recruitment region: Europe or outside of Europe (rest of world [RoW]). Progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and adverse events (AEs) were compared between regional subgroups.
In total, there were 320 eligible patients from Europe (cabozantinib, 167; everolimus, 153) and 338 from RoW (North America, 240 patients; Asia-Pacific, 86; Latin America, 12; randomized as cabozantinib, 163; everolimus, 175). PFS and OS were longer with cabozantinib than with everolimus and similar for the Europe and RoW subgroups. For PFS, the hazard ratio (HR) for cabozantinib versus everolimus was 0.54 for the Europe subgroup ( < .001) and 0.50 for the RoW subgroup ( < .001). For OS, the HR was 0.75 for the Europe subgroup ( = .034) and 0.69 for the RoW subgroup ( = .006). ORR in the Europe subgroup was 15% for cabozantinib and 3.9% for everolimus ( < .001). For the RoW subgroup, ORR was 20% for cabozantinib and 2.9% for everolimus ( < .001). Incidence of grade 3/4 AEs were similar for the Europe (cabozantinib, 74%; everolimus, 58%) and RoW subgroups (cabozantinib, 69%; everolimus, 64%).
In the METEOR trial, efficacy outcomes for patients recruited from European and non-European countries favored cabozantinib over everolimus. The efficacy and safety results for the regional subgroups were consistent with those of the overall METEOR population.
Meteor 是一项 3 期临床试验(NCT01865747),比较了卡博替尼与依维莫司在先前接受过血管内皮生长因子受体(VEGFR)酪氨酸激酶抑制剂(TKI)治疗的晚期或转移性透明细胞肾细胞癌(RCC)成人患者中的疗效。本项 Meteor 分析比较了来自欧洲和非欧洲国家招募的患者的结局。
入组的晚期/转移性透明细胞肾细胞癌患者接受过≥1 种 VEGFR-TKI 治疗,按 1:1 随机分组,分别接受卡博替尼或依维莫司治疗。根据招募区域将患者分为:欧洲或非欧洲地区(世界其他地区[RoW])。无进展生存期(PFS)、总生存期(OS)、客观缓解率(ORR)和不良事件(AEs)在区域亚组间进行比较。
共纳入欧洲地区(卡博替尼组 167 例,依维莫司组 153 例)和 RoW 地区(北美 240 例,亚太地区 86 例,拉丁美洲 12 例;随机分配为卡博替尼组 163 例,依维莫司组 175 例)各 320 例和 338 例合格患者。与依维莫司相比,卡博替尼可延长患者的 PFS 和 OS,且欧洲和 RoW 亚组间无显著差异。在 PFS 方面,卡博替尼组与依维莫司组的风险比(HR)为 0.54(<0.001),RoW 亚组为 0.50(<0.001)。OS 方面,卡博替尼组的 HR 为 0.75(=0.034),RoW 亚组为 0.69(=0.006)。在欧洲亚组中,卡博替尼的 ORR 为 15%,依维莫司为 3.9%(<0.001)。在 RoW 亚组中,卡博替尼的 ORR 为 20%,依维莫司为 2.9%(<0.001)。欧洲亚组(卡博替尼组 74%,依维莫司组 58%)和 RoW 亚组(卡博替尼组 69%,依维莫司组 64%)中 3/4 级不良事件的发生率相似。
在 Meteor 试验中,来自欧洲和非欧洲国家招募的患者的疗效结果倾向于卡博替尼优于依维莫司。区域亚组的疗效和安全性结果与总体 Meteor 人群一致。