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免疫检查点抑制剂新辅助治疗可切除肝细胞癌的疗效与安全性的Meta分析

Meta-analysis of the efficiency and safety of neoadjuvant therapy with immune checkpoint inhibitors in resectable hepatocellular carcinoma.

作者信息

Tuersun Adili, Yasen Yadikaer, Mohetaer Munire, Hou Guanxin, Cheng Gang, Zhao Xin

机构信息

School of Life Sciences and Biopharmaceutics, Shenyang Pharmaceutical University, Shenyang, Liaoning, China.

Department of Breast Surgery, Affiliated Tumor Hospital of xinjiang Medical University, Urumqi, China.

出版信息

Front Med (Lausanne). 2025 Jan 29;11:1511511. doi: 10.3389/fmed.2024.1511511. eCollection 2024.

Abstract

PURPOSE

Immunotherapy as a neoadjuvant treatment approach has achieved certain therapeutic effects in various types of cancer. However, in the specific cancer type of hepatocellular carcinoma (HCC), standardized protocols for neoadjuvant immunotherapy remain to be defined. This systematic review and meta-analysis focus on evaluating the efficacy and safety of neoadjuvant immunotherapy in the treatment of HCC, aiming to provide a robust basis for clinical decision-making.

METHODS

This study systematically searched databases such as PubMed, EMBASE, the Cochrane Library, and conference proceedings to identify clinical trials focusing on patients with HCC undergoing neoadjuvant immunotherapy. The Review Manager 5.4 software was applied to estimate the odds ratio (OR) of effect sizes and their corresponding 95% confidence intervals (CI).

RESULTS

Immune checkpoint inhibitors (ICIs) demonstrate significant efficacy in improving pathological outcomes and safety profiles in patients with resectable hepatocellular carcinoma (HCC). Specifically, ICIs significantly increase the pathological complete response (pCR) rate (OR = 0.23, 95% CI [0.14, 0.37],  < 0.00001) and major pathological response (MPR) rate (OR = 0.47, 95% CI [0.32, 0.70],  = 0.0002). They also markedly enhance the objective response rate (ORR) (OR = 0.42, 95% CI [0.28, 0.63],  < 0.0001). Furthermore, ICIs potentially improve the surgical resection rate (OR = 3.91, 95% CI [2.05, 7.45],  < 0.0001) and reduce the incidence of grade 3-4 treatment-related adverse events (TRAEs) (OR = 0.27, 95% CI [0.17, 0.44],  < 0.00001), indicating both therapeutic benefits and acceptable toxicity profiles.

CONCLUSION

Neoadjuvant immunotherapy shows promise in the treatment of resectable HCC. Nonetheless, to further validate its efficacy, more large-scale, well-designed clinical trials are necessary to provide conclusive evidence.

SYSTEMATIC REVIEW REGISTRATION

This comprehensive review adheres to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) standards and has been carried out as per a preregistered protocol (PROSPERO registration number: CRD42024560660).

摘要

目的

免疫疗法作为一种新辅助治疗方法,已在各类癌症中取得了一定的治疗效果。然而,在肝细胞癌(HCC)这种特定的癌症类型中,新辅助免疫疗法的标准化方案仍有待确定。本系统评价和荟萃分析旨在评估新辅助免疫疗法治疗HCC的疗效和安全性,为临床决策提供有力依据。

方法

本研究系统检索了PubMed、EMBASE、Cochrane图书馆等数据库以及会议论文集,以识别聚焦于接受新辅助免疫疗法的HCC患者的临床试验。应用Review Manager 5.4软件估计效应量的比值比(OR)及其相应的95%置信区间(CI)。

结果

免疫检查点抑制剂(ICI)在改善可切除肝细胞癌(HCC)患者的病理结局和安全性方面显示出显著疗效。具体而言,ICI显著提高了病理完全缓解(pCR)率(OR = 0.23,95%CI [0.14, 0.37],P < 0.00001)和主要病理缓解(MPR)率(OR = 0.47,95%CI [0.32, 0.70],P = 0.0002)。它们还显著提高了客观缓解率(ORR)(OR = 0.42,95%CI [0.28, 0.63],P < 0.0001)。此外,ICI可能提高手术切除率(OR = 3.91,95%CI [2.05, 7.45],P < 0.0001)并降低3 - 4级治疗相关不良事件(TRAE)的发生率(OR = 0.27,95%CI [0.17, 0.44],P < 0.00001),表明其既有治疗益处又有可接受的毒性特征。

结论

新辅助免疫疗法在可切除HCC的治疗中显示出前景。尽管如此,为进一步验证其疗效,需要更多大规模、设计良好的临床试验来提供确凿证据。

系统评价注册

本全面评价遵循PRISMA(系统评价和荟萃分析的首选报告项目)标准,并已按照预先注册的方案进行(PROSPERO注册号:CRD42024560660)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/461f/11814204/0acbf392cce5/fmed-11-1511511-g001.jpg

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