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仑伐替尼联合抗程序性死亡受体1(PD-1)抗体加经动脉化疗栓塞术治疗不可切除肝细胞癌:一项多中心回顾性研究

Lenvatinib Combined with Anti-PD-1 Antibodies Plus Transcatheter Arterial Chemoembolization for Unresectable Hepatocellular Carcinoma: A Multicenter Retrospective Study.

作者信息

Wu Jia-Yi, Yin Zhen-Yu, Bai Yan-Nan, Chen Yu-Feng, Zhou Song-Qiang, Wang Shuang-Jia, Zhou Jian-Yin, Li Yi-Nan, Qiu Fu-Nan, Li Bin, Yan Mao-Lin

机构信息

Shengli Clinical Medical College of Fujian Medical University, Fuzhou, Fujian Province, 350001, People's Republic of China.

Department of Hepatobiliary Pancreatic Surgery, Fujian Provincial Hospital, Fuzhou, Fujian Province, 350001, People's Republic of China.

出版信息

J Hepatocell Carcinoma. 2021 Oct 5;8:1233-1240. doi: 10.2147/JHC.S332420. eCollection 2021.

Abstract

BACKGROUND

Lenvatinib (LEN) combined with anti-PD-1 antibodies (PD-1) exerted promising effects on unresectable hepatocellular carcinoma (uHCC). We assessed the safety and clinical efficacy of triple therapy [LEN+PD-1+transcatheter arterial chemoembolization (TACE)] in uHCC.

METHODS

uHCC patients with an ECOG PS score of 0-1 and Child-Pugh class A who underwent triple therapy were included. The primary endpoint was objective response rate (ORR) based on mRECIST. Secondary endpoints were conversion rate to liver resection and treatment-related adverse events.

RESULTS

Between November 2018 and December 2020, 62 uHCC patients who underwent triple therapy at four major cancer centers in China were analyzed, including 35 in BCLC-C, 21 in BCLC-B, and 6 in BCLC-A. With a median follow-up of 12.2 months (range, 7.6-33.3 months), the investigator and blinded independent central review-assessed ORR were 80.6% and 77.4%, respectively. A total of 33 patients (53.2%) reached the standard of conversion to resectable HCC and 29 patients underwent resection. The median interval between start of triple therapy and resection was 123 days (range, 55-372 days). Pathological complete response and major pathological response were observed in 16 and 24 patients, respectively. Median overall survival and progression-free survival were not reached. Treatment-related adverse events occurred in 74.2% of the patients (grade ≥3, 14.5%; grade ≥4, 4.8%).

CONCLUSION

Combination of LEN, PD-1 and TACE showed a high rate of tumor response and convert resection in uHCC patients, with manageable toxicity.

摘要

背景

仑伐替尼(LEN)联合抗程序性死亡蛋白1(PD-1)抗体对不可切除肝细胞癌(uHCC)显示出有前景的疗效。我们评估了三联疗法[LEN+PD-1+经动脉化疗栓塞术(TACE)]治疗uHCC的安全性和临床疗效。

方法

纳入接受三联疗法、东部肿瘤协作组(ECOG)体能状态评分为0-1且Child-Pugh肝功能分级为A级的uHCC患者。主要终点是基于改良实体瘤疗效评价标准(mRECIST)的客观缓解率(ORR)。次要终点是转化为肝切除术的转化率和治疗相关不良事件。

结果

2018年11月至2020年12月期间,分析了在中国四个主要癌症中心接受三联疗法的62例uHCC患者,其中巴塞罗那临床肝癌(BCLC)-C期35例,BCLC-B期21例,BCLC-A期6例。中位随访12.2个月(范围7.6-33.3个月),研究者评估的ORR和盲态独立中央审查评估的ORR分别为80.6%和77.4%。共有33例患者(53.2%)达到转化为可切除肝癌的标准,29例患者接受了手术切除。三联疗法开始至切除的中位间隔时间为123天(范围55-372天)。分别有16例和24例患者观察到病理完全缓解和主要病理缓解。中位总生存期和无进展生存期未达到。74.2%的患者发生治疗相关不良事件(≥3级,14.5%;≥4级,4.8%)。

结论

LEN、PD-1和TACE联合应用在uHCC患者中显示出较高的肿瘤缓解率和转化切除率,且毒性可控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fd/8502053/a509e9335871/JHC-8-1233-g0001.jpg

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