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Transarterial chemoembolization with PD-(L)1 inhibitors plus molecular targeted therapies for hepatocellular carcinoma (CHANCE001).经动脉化疗栓塞术联合 PD-(L)1 抑制剂和分子靶向治疗肝癌(CHANCE001)。
Signal Transduct Target Ther. 2023 Feb 8;8(1):58. doi: 10.1038/s41392-022-01235-0.
2
Lenvatinib plus transarterial chemoembolization with or without immune checkpoint inhibitors for unresectable hepatocellular carcinoma: A review.乐伐替尼联合经动脉化疗栓塞术(无论是否联合免疫检查点抑制剂)治疗不可切除肝细胞癌的综述
Front Oncol. 2022 Sep 28;12:980214. doi: 10.3389/fonc.2022.980214. eCollection 2022.
3
Efficacy and safety of monotherapy and combination therapy of immune checkpoint inhibitors as first-line treatment for unresectable hepatocellular carcinoma: a systematic review, meta-analysis and network meta-analysis.免疫检查点抑制剂单药及联合治疗作为不可切除肝细胞癌一线治疗的疗效和安全性:一项系统评价、荟萃分析和网状荟萃分析
Discov Oncol. 2022 Sep 28;13(1):95. doi: 10.1007/s12672-022-00559-1.
4
Hepatic arterial infusion chemotherapy and sequential ablation treatment in large hepatocellular carcinoma.肝动脉灌注化疗联合序贯消融治疗巨大肝癌。
Int J Hyperthermia. 2022;39(1):1097-1105. doi: 10.1080/02656736.2022.2112307.
5
Lenvatinib Combined With Transarterial Chemoembolization as First-Line Treatment for Advanced Hepatocellular Carcinoma: A Phase III, Randomized Clinical Trial (LAUNCH).仑伐替尼联合经动脉化疗栓塞术作为晚期肝细胞癌一线治疗的III期随机临床试验(LAUNCH)
J Clin Oncol. 2023 Jan 1;41(1):117-127. doi: 10.1200/JCO.22.00392. Epub 2022 Aug 3.
6
Efficacy and Safety of Lenvatinib Combined With PD-1 Inhibitors Plus TACE for Unresectable Hepatocellular Carcinoma Patients in China Real-World.在中国真实世界中,乐伐替尼联合PD-1抑制剂加经动脉化疗栓塞术治疗不可切除肝细胞癌患者的疗效和安全性
Front Oncol. 2022 Jul 4;12:950266. doi: 10.3389/fonc.2022.950266. eCollection 2022.
7
PD-L1 Protein Expression Is Associated With Good Clinical Outcomes and Nomogram for Prediction of Disease Free Survival and Overall Survival in Breast Cancer Patients Received Neoadjuvant Chemotherapy.PD-L1 蛋白表达与乳腺癌患者接受新辅助化疗后的良好临床结局相关,且可用于无病生存和总生存的预测。
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8
Transarterial chemoembolization plus a PD-1 inhibitor with or without lenvatinib for intermediate-stage hepatocellular carcinoma.经动脉化疗栓塞联合PD-1抑制剂(联合或不联合乐伐替尼)治疗中期肝细胞癌
Hepatol Res. 2022 Aug;52(8):721-729. doi: 10.1111/hepr.13773. Epub 2022 May 22.
9
Efficacy and Safety of TACE Combined With Lenvatinib Plus PD-1 Inhibitors Compared With TACE Alone for Unresectable Hepatocellular Carcinoma Patients: A Prospective Cohort Study.经动脉化疗栓塞术(TACE)联合乐伐替尼及程序性死亡受体1(PD -1)抑制剂与单纯TACE治疗不可切除肝细胞癌患者的疗效和安全性比较:一项前瞻性队列研究
Front Oncol. 2022 Apr 21;12:874473. doi: 10.3389/fonc.2022.874473. eCollection 2022.
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Efficacy of Sorafenib Combined With Immunotherapy Following Transarterial Chemoembolization for Advanced Hepatocellular Carcinoma: A Propensity Score Analysis.经动脉化疗栓塞术后索拉非尼联合免疫治疗对晚期肝细胞癌的疗效:一项倾向评分分析
Front Oncol. 2022 Apr 8;12:807102. doi: 10.3389/fonc.2022.807102. eCollection 2022.

不可切除肝细胞癌中经动脉化疗栓塞联合仑伐替尼,以及联合与不联合 PD-1 抑制剂的预后列线图模型。

Prognostic nomogram model for selecting between transarterial chemoembolization plus lenvatinib, with and without PD-1 inhibitor in unresectable hepatocellular carcinoma.

机构信息

Department of Interventional Radiology, Third Affiliated Hospital of Soochow University & Changzhou First People's Hospital, Juqian street NO.185, Tianning district, Changzhou, Jiangsu, 213003, China.

Department of Radiology, Third Affiliated Hospital of Soochow University, Changzhou & Changzhou First People's Hospital, Juqian street NO.185, Tianning district, Changzhou, Jiangsu, 213003, China.

出版信息

Br J Radiol. 2024 Feb 28;97(1155):668-679. doi: 10.1093/bjr/tqae018.

DOI:10.1093/bjr/tqae018
PMID:38303541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11027259/
Abstract

OBJECTIVES

To establish and verify a prognostic nomogram model for selecting in unresectable hepatocellular carcinoma (uHCC) treated by transarterial chemoembolization plus lenvatinib (TACE-L) with or without PD-1 inhibitor.

METHODS

Data of 241 uHCC patients who underwent TACE-L (n = 128) and TACE-L plus PD-1 inhibitor (TACE-L-P, n = 113) were retrospectively reviewed. The differences in tumour responses, progression-free survival (PFS), overall survival (OS), and adverse events (AEs) between two groups were compared, and a prognostic nomogram model was established based on independent clinical-radiologic factors and confirmed by Cox regression analysis for predicting PFS and OS. The treatment selection for uHCC patients was stratified by the nomogram score.

RESULTS

Compared to TACE-L, TACE-L-P presented prolonged PFS (14.0 vs. 9.0 months, P < .001), longer OS (24.0 vs. 15.0 months, P < .001), and a better overall objective response rate (54.0% vs. 32.8%, P = .001). There was no significant difference between the rate of AEs in the TACE-L-P and the TACE-L (56.64% vs. 46.09%, P = .102) and the rate of grade ≥ 3 AEs (11.50% vs. 9.38%, P = .588), respectively. The nomogram model presented good discrimination, with a C-index of 0.790 for predicting PFS and 0.749 for predicting OS. Patients who underwent TACE-L and obtained a nomogram score >9 demonstrated improved 2-year PFS when transferred to TACE-L-P, and those with a nomogram ≤25 had better 2-year OS when transferred to TACE-L-P.

CONCLUSIONS

TACE-L-P showed significant improvements in efficiency and safety for uHCC patients compared with TACE-L. The nomogram was useful for stratifying treatment decisions and selecting a suitable population for uHCC patients.

ADVANCES IN KNOWLEDGE

Prognostic nomogram model is of great value in predicting individualized survival benefits for uHCC patients after TACE-L or/and TACE-L-P. And the nomogram was helpful for selection between TACE-L-P and TACE-L among uHCC patients.

摘要

目的

建立并验证一个用于选择接受经动脉化疗栓塞联合仑伐替尼(TACE-L)治疗的不可切除肝细胞癌(uHCC)患者的预后列线图模型,这些患者联合或不联合 PD-1 抑制剂治疗。

方法

回顾性分析了 241 例接受 TACE-L(n=128)和 TACE-L 联合 PD-1 抑制剂(TACE-L-P,n=113)治疗的 uHCC 患者的数据。比较两组患者的肿瘤反应、无进展生存期(PFS)、总生存期(OS)和不良事件(AE)差异,并基于独立的临床影像学因素建立预后列线图模型,通过 Cox 回归分析进行验证,以预测 PFS 和 OS。根据列线图评分对 uHCC 患者的治疗选择进行分层。

结果

与 TACE-L 相比,TACE-L-P 组患者的 PFS 更长(14.0 个月比 9.0 个月,P<0.001),OS 更长(24.0 个月比 15.0 个月,P<0.001),总客观缓解率更高(54.0%比 32.8%,P=0.001)。TACE-L-P 组和 TACE-L 组的 AE 发生率(56.64%比 46.09%,P=0.102)和≥3 级 AE 发生率(11.50%比 9.38%,P=0.588)无显著差异。列线图模型具有良好的区分度,预测 PFS 的 C 指数为 0.790,预测 OS 的 C 指数为 0.749。在接受 TACE-L 治疗且列线图评分>9 的患者中,转为 TACE-L-P 治疗可提高 2 年 PFS,而在列线图评分≤25 的患者中,转为 TACE-L-P 治疗可提高 2 年 OS。

结论

与 TACE-L 相比,TACE-L-P 可显著提高 uHCC 患者的疗效和安全性。该列线图模型可用于分层治疗决策,并为 uHCC 患者选择合适的人群。

知识进展

预后列线图模型对于预测接受 TACE-L 或/和 TACE-L-P 治疗后的 uHCC 患者的个体化生存获益具有重要价值。并且该列线图有助于在 uHCC 患者中选择 TACE-L-P 与 TACE-L 之间的治疗方案。