Department of Medical Oncology, Yonsei Cancer Center, Yonsei University Health System, Seoul, South Korea.
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Int J Cancer. 2023 Sep 15;153(6):1241-1250. doi: 10.1002/ijc.34608. Epub 2023 Jun 9.
In the CLEAR trial, lenvatinib plus pembrolizumab met study endpoints of superiority vs sunitinib in the first-line treatment of patients with advanced renal cell carcinoma. We report the efficacy and safety results of the East Asian subset (ie, patients in Japan and the Republic of Korea) from the CLEAR trial. Of 1069 patients randomly assigned to receive either lenvatinib plus pembrolizumab, lenvatinib plus everolimus or sunitinib, 213 (20.0%) were from East Asia. Baseline characteristics of patients in the East Asian subset were generally comparable with those of the global trial population. In the East Asian subset, progression-free survival was considerably longer with lenvatinib plus pembrolizumab vs sunitinib (median 22.1 vs 11.1 months; HR 0.38; 95% CI: 0.23-0.62). The HR for overall survival comparing lenvatinib plus pembrolizumab vs sunitinib was 0.71; 95% CI: 0.30-1.71. The objective response rate was higher with lenvatinib plus pembrolizumab vs sunitinib (65.3% vs 49.2%; odds ratio 2.14; 95% CI: 1.07-4.28). Dose reductions due to treatment-emergent adverse events (TEAEs) commonly associated with tyrosine kinase inhibitors occurred more frequently than in the global population. Hand-foot syndrome was the most frequent any-grade TEAE with lenvatinib plus pembrolizumab (66.7%) and sunitinib (57.8%), a higher incidence compared to the global population (28.7% and 37.4%, respectively). The most common grade 3 to 5 TEAEs were hypertension with lenvatinib plus pembrolizumab (20%) and decreased platelet count with sunitinib (21.9%). Efficacy and safety for patients in the East Asian subset were generally similar to those of the global population, except as noted.
在 CLEAR 试验中,仑伐替尼联合 pembrolizumab 在一线治疗晚期肾细胞癌患者方面优于舒尼替尼。我们报告了 CLEAR 试验东亚亚组(即来自日本和韩国的患者)的疗效和安全性结果。在随机接受仑伐替尼联合 pembrolizumab、仑伐替尼联合依维莫司或舒尼替尼治疗的 1069 名患者中,有 213 名(20.0%)来自东亚。东亚亚组患者的基线特征与全球试验人群基本一致。在东亚亚组中,仑伐替尼联合 pembrolizumab 与舒尼替尼相比,无进展生存期显著延长(中位 22.1 个月 vs 11.1 个月;HR 0.38;95%CI:0.23-0.62)。仑伐替尼联合 pembrolizumab 与舒尼替尼相比,总生存期的 HR 为 0.71;95%CI:0.30-1.71。仑伐替尼联合 pembrolizumab 与舒尼替尼相比,客观缓解率更高(65.3% vs 49.2%;OR 2.14;95%CI:1.07-4.28)。与酪氨酸激酶抑制剂相关的常见治疗相关不良事件(TEAEs)导致的剂量减少比全球人群更频繁。仑伐替尼联合 pembrolizumab(66.7%)和舒尼替尼(57.8%)最常见的任何级别 TEAEs 是手足综合征,发生率高于全球人群(分别为 28.7%和 37.4%)。仑伐替尼联合 pembrolizumab 最常见的 3 级至 5 级 TEAEs 是高血压(20%),舒尼替尼最常见的是血小板计数减少(21.9%)。东亚亚组患者的疗效和安全性与全球人群总体相似,但也存在一些差异。