Gustave Roussy, Villejuif, France.
Centre Léon Bérard, Lyon, France.
Eur J Cancer. 2021 Jan;142:102-111. doi: 10.1016/j.ejca.2020.09.030. Epub 2020 Nov 27.
Real-world data on cabozantinib in metastatic renal cell carcinoma (mRCC) is limited. This study (CABOREAL) reports treatment patterns and outcomes for patients treated with cabozantinib through the French Early Access Program.
This multicentre (n = 26), observational, retrospective study enrolled patients with mRCC who had received ≥1 dose of cabozantinib. Overall survival (OS) was estimated using the Kaplan-Meier method; subgroups were compared using the log-rank test. A multiple Cox regression model assessed predictive factors of OS after cabozantinib initiation.
Four hundred and ten recruited patients started treatment between September 2016 and February 2018: the Eastern Cooperative Oncology Group Performance Status ≥2, 39.3%; poor International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk, 31.7%; 0-1, 2 and ≥3 previous treatment lines, 25.3%, 33.4% and 41.2%, respectively; bone metastases, 55.9%; brain metastases, 16.8%. Median (min-max) follow-up was 14.4 (0-30) months. Overall, 57.0% of patients had a dose reduction, 15.6% an alternative dose schedule. The median average daily dose was 40.0 mg. Median (quartile [Q]1-Q3) treatment duration was 7.6 (0.1-29.1) months, median OS was 14.4 months, and the 12-month OS rate was 56.5% (95% confidence interval: 51.5-61.2). Most patients (54.4%) received subsequent treatment. Predictive factors associated with longer OS were body mass index ≥25 kg/m (p = 0.0021), prior nephrectomy (p = 0.0109), favourable or intermediate IMDC risk (p < 0.0001) and cabozantinib initiation at 60 mg/day (p = 0.0486).
In the largest real-world study to date, cabozantinib was effective in unselected, heavily pretreated patients with mRCC. Initiation at 60 mg/day was associated with improved outcomes. CLINICALTRIALS.
NCT03744585.
转移性肾细胞癌(mRCC)的卡博替尼真实世界数据有限。本研究(CABOREAL)报告了通过法国早期准入计划接受卡博替尼治疗的患者的治疗模式和结局。
这是一项多中心(n=26)、观察性、回顾性研究,纳入了接受过至少 1 剂卡博替尼治疗的 mRCC 患者。使用 Kaplan-Meier 法估计总生存期(OS);使用对数秩检验比较亚组。采用多因素 Cox 回归模型评估卡博替尼起始后 OS 的预测因素。
410 名招募的患者于 2016 年 9 月至 2018 年 2 月期间开始治疗:东部合作肿瘤组表现状态(ECOG PS)≥2,占 39.3%;国际转移性肾细胞癌数据库联盟(IMDC)风险差,占 31.7%;0-1、2 和≥3 条治疗线,分别占 25.3%、33.4%和 41.2%;骨转移,占 55.9%;脑转移,占 16.8%。中位(最小-最大)随访时间为 14.4(0-30)个月。总体而言,57.0%的患者减少了剂量,15.6%改变了替代剂量方案。平均日剂量中位数为 40.0mg。中位(四分位数[Q]1-Q3)治疗持续时间为 7.6(0.1-29.1)个月,中位 OS 为 14.4 个月,12 个月 OS 率为 56.5%(95%置信区间:51.5-61.2)。大多数患者(54.4%)接受了后续治疗。与更长 OS 相关的预测因素包括体重指数(BMI)≥25kg/m2(p=0.0021)、先前的肾切除术(p=0.0109)、有利或中等 IMDC 风险(p<0.0001)和卡博替尼起始剂量为 60mg/天(p=0.0486)。
在迄今为止最大的真实世界研究中,卡博替尼在未经选择的、大量预处理的 mRCC 患者中是有效的。起始剂量为 60mg/天与改善的结局相关。临床试验。
NCT03744585。