Beijing Ditan Hosipital, 12517Capital Medical University, Beijing, China.
Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221075174. doi: 10.1177/15330338221075174.
: We assessed the efficacy and safety of transarterial chemoembolization (TACE) in combination with lenvatinib plus programmed death receptor-1 (PD-1) signaling inhibitors (camrelizumab or sintilimab) in unresectable hepatocellular carcinoma (uHCC). : In this retrospective study, patients with uHCC were pretreated with lenvatinib for 1 to 2 weeks before TACE. Camrelizumab or sintilimab were initially administered intravenously in 1 week after TACE of a 21-day cycle. Primary objectives were objective response rate (ORR) and disease control rate (DCR) by modified Response Evaluation Criteria in Solid Tumors (mRECIST). The secondary endpoints included the progression-free survival (PFS), overall survival (OS), and toxicity. : Between March 5, 2019 and February 30, 2021, 53 patients were screened for eligibility. At data cutoff, 35.8% of patients remained on treatment. Median follow-up was 15.4 months. Confirmed ORR in the 51 evaluable patients was 54.9% (95% CI 41.4%-67.7%). DCR was 84.3% (95% CI 72.0%-91.8%). Median PFS was 8.5 months (95% CI 6.4 to 10.6 months). The median OS was not estimable. Grade ≥3 treatment-related adverse events occurred in 32.1% of patients. No new safety signals were identified. : TACE in combination with lenvatinib plus anti-PD-1 inhibitors may have promising antitumor activity in uHCC. Toxicities were manageable, with no unexpected safety signals.
我们评估了经动脉化疗栓塞(TACE)联合仑伐替尼加程序性死亡受体-1(PD-1)信号抑制剂(卡瑞利珠单抗或替雷利珠单抗)治疗不可切除肝细胞癌(uHCC)的疗效和安全性。
在这项回顾性研究中,uHCC 患者在 TACE 前接受仑伐替尼治疗 1 至 2 周。在 TACE 后第 1 周,以 21 天为一个周期,开始静脉注射卡瑞利珠单抗或替雷利珠单抗。主要终点为改良实体瘤反应评估标准(mRECIST)的客观缓解率(ORR)和疾病控制率(DCR)。次要终点包括无进展生存期(PFS)、总生存期(OS)和毒性。
2019 年 3 月 5 日至 2021 年 2 月 30 日,共筛选了 53 例符合条件的患者。截至数据截止日期,35.8%的患者仍在接受治疗。中位随访时间为 15.4 个月。在 51 例可评估患者中,确认的 ORR 为 54.9%(95%CI 41.4%-67.7%)。DCR 为 84.3%(95%CI 72.0%-91.8%)。中位 PFS 为 8.5 个月(95%CI 6.4 至 10.6 个月)。中位 OS 不可估计。32.1%的患者发生≥3 级治疗相关不良事件。未发现新的安全性信号。
TACE 联合仑伐替尼加抗 PD-1 抑制剂在 uHCC 中可能具有有前途的抗肿瘤活性。毒性可管理,没有意外的安全信号。