Hepatic arterial infusion chemotherapy combined with systemic therapy sequentially or simultaneously for advanced hepatocellular carcinoma.

IF 4.6 2区 医学 Q2 IMMUNOLOGY Cancer Immunology, Immunotherapy Pub Date : 2024-11-14 DOI:10.1007/s00262-024-03872-6
Yu-Zhe Cao, Jia-Yu Pan, Guang-Lei Zheng, Chao An, Meng-Xuan Zuo
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Abstract

Background and aims: The goal of this study was to compare the efficacy and safety of hepatic arterial infusion chemotherapy (HAIC) combined with targeted therapy and PD-(L)1 blockade (triple therapy), either sequentially (SE) or simultaneously (SI), in the treatment of Barcelona Clinic Liver Cancer (BCLC) stage C hepatocellular carcinoma (HCC).

Approach and results: From January 1, 2018, to June 1, 2022, 575 patients with BCLC stage C HCC who underwent SE or SI triple therapy were retrospectively enrolled. Propensity score matching (PSM; 1:1) was performed to eliminate possible confounder imbalances across cohorts. We used the Kaplan-Meier method and a log-rank test to compare the overall survival (OS) and progression-free survival (PFS) rates between the SI and SE groups. The tumor response and the incidence of adverse events (AEs) were reported. After PSM, 182 patients in each of the two groups were matched. The median OS in the SI group was significantly longer than that in the SE group (28.8 vs. 16.1 months; P = 0.002), and the median PFS was significantly improved in the SI versus SE group (9.6 vs. 7.0 months; P = 0.01). The objective response rate based on the mRECIST was higher in the SI group (58% vs. 37%; P < 0.001). The total incidences of grade 3-4 AEs were 111/182 (60.9%) and 128/182 (70.3%) in the SE and SI groups, respectively. No grade 5 AEs were reported in either group.

Conclusions: Simultaneous HAIC plus targeted therapy and PD-(L)1 blockade significantly improved outcomes compared to the sequential regimen in patients with BCLC stage C HCC, with no unexpected AEs.

Clinical relevance statement: The patients who received hepatic arterial infusion chemotherapy combined with targeted therapy and PD-(L)1 blockade simultaneously have a better prognosis than those who received it sequentially.

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肝动脉灌注化疗与全身治疗相继或同时治疗晚期肝细胞癌。
背景和目的:本研究旨在比较肝动脉灌注化疗(HAIC)联合靶向治疗和PD-(L)1阻断(三联疗法)序贯(SE)或同步(SI)治疗巴塞罗那肝癌诊所(BCLC)C期肝细胞癌(HCC)的疗效和安全性:从2018年1月1日至2022年6月1日,回顾性纳入了575例接受SE或SI三联疗法的BCLC C期HCC患者。我们进行了倾向得分匹配(PSM;1:1),以消除各队列中可能存在的混杂因素不平衡。我们采用卡普兰-梅耶法和对数秩检验比较了SI组和SE组的总生存期(OS)和无进展生存期(PFS)。我们还报告了肿瘤反应和不良事件(AEs)的发生率。PSM 后,两组各有 182 名患者进行了配对。SI组的中位OS明显长于SE组(28.8个月对16.1个月;P = 0.002),SI组的中位PFS明显优于SE组(9.6个月对7.0个月;P = 0.01)。基于mRECIST的客观反应率在SI组更高(58% vs. 37%; P 结论:SI组的客观反应率高于SE组:对于 BCLC C 期 HCC 患者,HAIC 加靶向治疗和 PD-(L)1 阻断同时进行可显著改善预后,且无意外 AEs:同时接受肝动脉灌注化疗联合靶向治疗和PD-(L)1阻断治疗的患者比顺序接受治疗的患者预后更好。
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来源期刊
CiteScore
10.50
自引率
1.70%
发文量
207
审稿时长
1 months
期刊介绍: Cancer Immunology, Immunotherapy has the basic aim of keeping readers informed of the latest research results in the fields of oncology and immunology. As knowledge expands, the scope of the journal has broadened to include more of the progress being made in the areas of biology concerned with biological response modifiers. This helps keep readers up to date on the latest advances in our understanding of tumor-host interactions. The journal publishes short editorials including "position papers," general reviews, original articles, and short communications, providing a forum for the most current experimental and clinical advances in tumor immunology.
期刊最新文献
HLA-G high-expressor 3'UTR markers are linked to gastric cancer development and survival. Hepatitis associated with immune checkpoint inhibitors-based combinations of other therapies: A real-world pharmacovigilance analysis based on the FDA adverse event reporting system (FAERS) database. Hepatic arterial infusion chemotherapy combined with systemic therapy sequentially or simultaneously for advanced hepatocellular carcinoma. "Tumor immunology meets oncology" (TIMO), 18 April-20 April 2024, in Brandenburg an der Havel, Germany. Cryo-thermal therapy reshaped the tumor immune microenvironment to enhance the efficacy of adoptive T cell therapy.
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