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经动脉化疗栓塞联合卡瑞利珠单抗治疗复发性肝细胞癌。

Transarterial chemoembolization combined with camrelizumab for recurrent hepatocellular carcinoma.

机构信息

Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.

Hubei Province Key Laboratory of Molecular Imaging, Wuhan, 430022, China.

出版信息

BMC Cancer. 2022 Mar 14;22(1):270. doi: 10.1186/s12885-022-09325-6.

Abstract

PURPOSE

To evaluate the efficacy and safety of transarterial chemoembolization (TACE) combined with camrelizumab (hereafter, TACE-camrelizumab) in the treatment of patients with recurrent hepatocellular carcinoma (R-HCC) after curative resection.

PATIENTS AND METHODS

R-HCC patients who underwent TACE plus camrelizumab or TACE-alone from January 2016 to August 2021 were retrospectively evaluated. Patients were assessed for tumor response, progression-free survival, survival rates and adverse events.

RESULTS

Seventy-one patients were included in this study, including 20 patients in the TACE- camrelizumab group and 51 patients in the TACE-alone group. The objective response rate was 56.9% in the TACE-alone group and 40% in the TACE-camrelizumab group at 3 months (P = 0.201). The disease control rates were 84.3% in TACE-alone group and 80% in TACE-camrelizumab group at 3 months (P = 0.663). The progression-free survival (PFS) of the TACE-alone group was slightly longer than those of the TACE- camrelizumab group (9 months vs. 6 months). However, there were no statistically significant differences in the median PFS (P = 0.586). Similarly, there were no significant differences in the half-year and one-year survival rates (P = 0.304, P = 0.430). Multivariate analysis revealed that Neutrophil-to-lymphocyte ratio (NLR) was associated with PFS significantly. 75% patients developed at least one type of AEs related to camrelizumab in TACE-camrelizumab group, and no patients developed severe AEs.

CONCLUSION

Comparing with TACE-Alone, the efficacy of TACE-camrelizumab for patients with R-HCC was similar. Meanwhile, the results of this study also indicated that TACE is still a better choice for patients with R-HCC.

摘要

目的

评估经动脉化疗栓塞(TACE)联合卡瑞利珠单抗(以下简称 TACE-卡瑞利珠单抗)治疗根治性切除术后复发性肝细胞癌(R-HCC)患者的疗效和安全性。

方法

回顾性评估了 2016 年 1 月至 2021 年 8 月期间接受 TACE 联合卡瑞利珠单抗或 TACE 单药治疗的 R-HCC 患者。评估了患者的肿瘤反应、无进展生存期、生存率和不良事件。

结果

本研究共纳入 71 例患者,其中 TACE-卡瑞利珠单抗组 20 例,TACE 单药组 51 例。TACE 单药组 3 个月时客观缓解率为 56.9%,TACE-卡瑞利珠单抗组为 40%(P=0.201)。TACE 单药组的疾病控制率为 84.3%,TACE-卡瑞利珠单抗组为 80%(P=0.663)。TACE 单药组的无进展生存期(PFS)略长于 TACE-卡瑞利珠单抗组(9 个月 vs. 6 个月)。然而,中位 PFS 无统计学差异(P=0.586)。同样,半年和一年生存率也无显著差异(P=0.304,P=0.430)。多因素分析显示,中性粒细胞与淋巴细胞比值(NLR)与 PFS 显著相关。TACE-卡瑞利珠单抗组有 75%的患者发生至少一种与卡瑞利珠单抗相关的 AEs,无患者发生严重 AEs。

结论

与 TACE 单药治疗相比,TACE-卡瑞利珠单抗治疗 R-HCC 患者的疗效相似。同时,本研究结果也表明 TACE 仍是 R-HCC 患者的更好选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13af/8922827/38b09dc18584/12885_2022_9325_Fig1_HTML.jpg

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