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经动脉化疗栓塞联合免疫检查点抑制剂加仑伐替尼治疗不可切除肝细胞癌的回顾性研究。

A Retrospective Study on Therapeutic Efficacy of Transarterial Chemoembolization Combined With Immune Checkpoint Inhibitors Plus Lenvatinib in Patients With Unresectable Hepatocellular Carcinoma.

机构信息

Beijing Ditan Hosipital, 12517Capital Medical University, Beijing, China.

出版信息

Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221075174. doi: 10.1177/15330338221075174.

Abstract

: 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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fe7/8943530/ac5e5fd60e0d/10.1177_15330338221075174-fig1.jpg

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