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Lenvatinib Combined with Anti-PD-1 Antibodies Plus Transcatheter Arterial Chemoembolization for Unresectable Hepatocellular Carcinoma: A Multicenter Retrospective Study
被引:89
|作者:
Wu, Jia-Yi
[1
,2
]
Yin, Zhen-Yu
[3
]
Bai, Yan-Nan
[1
,2
]
Chen, Yu-Feng
[4
]
Zhou, Song-Qiang
[1
,2
]
Wang, Shuang-Jia
[5
]
Zhou, Jian-Yin
[6
]
Li, Yi-Nan
[2
]
Qiu, Fu-Nan
[1
,2
]
Li, Bin
[5
]
Yan, Mao-Lin
[1
,2
]
机构:
[1] Fujian Med Univ, Shengli Clin Med Coll, Fuzhou 350001, Fujian, Peoples R China
[2] Fujian Prov Hosp, Dept Hepatobiliary Pancreat Surg, Fuzhou 350001, Fujian, Peoples R China
[3] Xiamen Tradit Chinese Med Hosp, Dept Hepatobiliary Surg, Xiamen 361000, Fujian, Peoples R China
[4] Fujian Med Univ, Dept Hepatobiliary Surg, Zhangzhou Affiliated Hosp, Zhangzhou 363000, Fujian, Peoples R China
[5] Xiamen Univ, Dept Hepatobiliary Pancreat & Vasc Surg, Affiliated Hosp 1, Xiamen 361000, Fujian, Peoples R China
[6] Xiamen Univ, Dept Hepatobiliary Surg, Zhongshan Hosp, Xiamen 361000, Fujian, Peoples R China
关键词:
unresectable hepatocellular carcinoma;
tumor response;
adverse events;
combination therapy;
monotherapy;
CLINICAL-PRACTICE GUIDELINES;
MANAGEMENT;
SORAFENIB;
RESECTION;
ASIA;
D O I:
10.2147/JHC.S332420
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
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.
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页码:1233 / 1240
页数:8
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