PD-1/PD-L1抑制剂在不可切除肝癌降期转化治疗中的机制研究进展
Progress in Research on the Mechanism of PD-1/PD-L1 Inhibitors in Down-Stage Conversion Therapy of Unresectable Liver Cancer
DOI: 10.12677/acm.2025.1551481, PDF,    国家自然科学基金支持
作者: 苗 舜, 赵开心, 李宏旭, 潘家鑫, 边树林, 魏思东*, 陈国勇*:河南省人民医院肝胆胰腺外科六病区,河南 郑州
关键词: 不可切除肝癌PD-1/PD-L1抑制剂转化治疗机制Unresectable Liver Cancer PD-1/PD-L1 Inhibitors Conversion Therapy Mechanism
摘要: 中国大多数原发性肝癌患者初诊时已是中晚期,失去了手术治疗的机会。针对不可切除肝细胞癌(Hepatocellular carcinoma, HCC)患者,局部介入治疗(如经动脉化疗栓塞术)和/或系统治疗(靶向药物、免疫治疗)可使肿瘤降期,从而使患者获得潜在手术干预机会及长期生存可能。近年来,肿瘤免疫微环境的动态调控机制逐渐被揭示,以免疫检查点抑制剂为代表的免疫治疗策略推动HCC治疗范式发生革命性突破。转化治疗对于大多数HCC患者而言,PD-1/PD-L1通路并不是抗肿瘤免疫的唯一限速因素。因此,联合治疗可能是更好的选择。本文解释了转化治疗的内涵,回顾了HCC患者免疫微环境的变化,对PD-1/PD-L1抑制剂的作用机制以及PD-1/PD-L1抑制剂联合用药作用机制进行总结,并列举联合治疗的案例及临床试验。
Abstract: Most patients with primary liver cancer in China are in the advanced stages when they are first diagnosed and have lost the opportunity for surgical treatment. For patients with unresectable hepatocellular carcinoma (HCC), local interventional therapy (such as transarterial chemoembolization) and/or systemic therapy (targeted drugs, immunotherapy) can reduce the tumor, thereby giving patients potential surgical intervention opportunities and long-term survival possibilities. In recent years, the dynamic regulation mechanisms of the tumor immune microenvironment have been gradually revealed, and immunotherapy strategies represented by immune checkpoint inhibitors have promoted revolutionary breakthroughs in the HCC treatment paradigm. At present, immunotherapy based on the programmed cell death protein-1 (PD-1)/programmed cell death protein ligand-1 (PD-L1) axis has achieved unprecedented success in HCC, but it also faces huge challenges, and its low response rate still needs to be resolved. For most HCC patients, the PD-1/PD-L1 pathway is not the only rate-limiting factor in anti-tumor immunity in conversion therapy. Therefore, combination therapy may be a better option. This article explains the content of conversion therapy, reviews the changes in the immune microenvironment of HCC patients, summarizes the mechanism of action of PD-1/PD-L1 inhibitors and the mechanism of action of PD-1/PD-L1 inhibitors combination, and lists cases and clinical trials of combination therapy.
文章引用:苗舜, 赵开心, 李宏旭, 潘家鑫, 边树林, 魏思东, 陈国勇. PD-1/PD-L1抑制剂在不可切除肝癌降期转化治疗中的机制研究进展[J]. 临床医学进展, 2025, 15(5): 1188-1200. https://doi.org/10.12677/acm.2025.1551481

参考文献

[1] Yang, J.D., Hainaut, P., Gores, G.J., Amadou, A., Plymoth, A. and Roberts, L.R. (2019) A Global View of Hepatocellular Carcinoma: Trends, Risk, Prevention and Management. Nature Reviews Gastroenterology & Hepatology, 16, 589-604. [Google Scholar] [CrossRef] [PubMed]
[2] Zhou, M., Wang, H., Zeng, X., Yin, P., Zhu, J., Chen, W., et al. (2019) Mortality, Morbidity, and Risk Factors in China and Its Provinces, 1990-2017: A Systematic Analysis for the Global Burden of Disease Study 2017. The Lancet, 394, 1145-1158. [Google Scholar] [CrossRef] [PubMed]
[3] Zhou, J., Sun, H., Wang, Z., Cong, W., Wang, J., Zeng, M., et al. (2020) Guidelines for the Diagnosis and Treatment of Hepatocellular Carcinoma (2019 Edition). Liver Cancer, 9, 682-720. [Google Scholar] [CrossRef] [PubMed]
[4] Sun, H., Zhou, J., Wang, Z., Liu, X., Xie, Q., Jia, W., et al. (2022) Chinese Expert Consensus on Conversion Therapy for Hepatocellular Carcinoma (2021 Edition). Hepatobiliary Surgery and Nutrition, 11, 227-252. [Google Scholar] [CrossRef] [PubMed]
[5] Zhou, H. and Song, T. (2021) Conversion Therapy and Maintenance Therapy for Primary Hepatocellular Carcinoma. BioScience Trends, 15, 155-160. [Google Scholar] [CrossRef] [PubMed]
[6] Sun, H. and Zhu, X. (2021) Downstaging Conversion Therapy in Patients with Initially Unresectable Advanced Hepatocellular Carcinoma: An Overview. Frontiers in Oncology, 11, Article 772195. [Google Scholar] [CrossRef] [PubMed]
[7] Chen, L. (2004) Co-Inhibitory Molecules of the B7-CD28 Family in the Control of T-Cell Immunity. Nature Reviews Immunology, 4, 336-347. [Google Scholar] [CrossRef] [PubMed]
[8] Intlekofer, A.M. and Thompson, C.B. (2013) At the Bench: Preclinical Rationale for CTLA-4 and PD-1 Blockade as Cancer Immunotherapy. Journal of Leukocyte Biology, 94, 25-39. [Google Scholar] [CrossRef] [PubMed]
[9] Chew, V., Lai, L., Pan, L., Lim, C.J., Li, J., Ong, R., et al. (2017) Delineation of an Immunosuppressive Gradient in Hepatocellular Carcinoma Using High-Dimensional Proteomic and Transcriptomic Analyses. Proceedings of the National Academy of Sciences of the United States of America, 114, E5900-E5909. [Google Scholar] [CrossRef] [PubMed]
[10] Noy, R. and Pollard, J.W. (2014) Tumor-Associated Macrophages: From Mechanisms to Therapy. Immunity, 41, 49-61. [Google Scholar] [CrossRef] [PubMed]
[11] Huang, Y., Ge, W., Zhou, J., Gao, B., Qian, X. and Wang, W. (2021) The Role of Tumor Associated Macrophages in Hepatocellular Carcinoma. Journal of Cancer, 12, 1284-1294. [Google Scholar] [CrossRef] [PubMed]
[12] Lu, C., Rong, D., Zhang, B., Zheng, W., Wang, X., Chen, Z., et al. (2019) Current Perspectives on the Immunosuppressive Tumor Microenvironment in Hepatocellular Carcinoma: Challenges and Opportunities. Molecular Cancer, 18, Article No. 130. [Google Scholar] [CrossRef] [PubMed]
[13] Cai, J., Wang, D., Zhang, G. and Guo, X. (2019) The Role of PD-1/PD-L1 Axis in Treg Development and Function: Implications for Cancer Immunotherapy. OncoTargets and Therapy, 12, 8437-8445. [Google Scholar] [CrossRef] [PubMed]
[14] Boussiotis, V.A. (2016) Molecular and Biochemical Aspects of the PD-1 Checkpoint Pathway. New England Journal of Medicine, 375, 1767-1778. [Google Scholar] [CrossRef] [PubMed]
[15] Yokosuka, T., Takamatsu, M., Kobayashi-Imanishi, W., Hashimoto-Tane, A., Azuma, M. and Saito, T. (2012) Programmed Cell Death 1 Forms Negative Costimulatory Microclusters That Directly Inhibit T Cell Receptor Signaling by Recruiting Phosphatase SHP2. Journal of Experimental Medicine, 209, 1201-1217. [Google Scholar] [CrossRef] [PubMed]
[16] Sharpe, A.H. and Pauken, K.E. (2017) The Diverse Functions of the PD1 Inhibitory Pathway. Nature Reviews Immunology, 18, 153-167. [Google Scholar] [CrossRef] [PubMed]
[17] Li, B., Yan, C., Zhu, J., Chen, X., Fu, Q., Zhang, H., et al. (2020) Anti-PD-1/PD-L1 Blockade Immunotherapy Employed in Treating Hepatitis B Virus Infection-Related Advanced Hepatocellular Carcinoma: A Literature Review. Frontiers in Immunology, 11, Article 1037. [Google Scholar] [CrossRef] [PubMed]
[18] Daassi, D., Mahoney, K.M. and Freeman, G.J. (2020) The Importance of Exosomal PDL1 in Tumour Immune Evasion. Nature Reviews Immunology, 20, 209-215. [Google Scholar] [CrossRef] [PubMed]
[19] Zhang, L., Zhang, M., Xu, J., Li, S., Chen, Y., Wang, W., et al. (2020) The Role of the Programmed Cell Death Protein-1/Programmed Death-Ligand 1 Pathway, Regulatory T Cells and T Helper 17 Cells in Tumor Immunity: A Narrative Review. Annals of Translational Medicine, 8, 1526-1526. [Google Scholar] [CrossRef] [PubMed]
[20] Xiao, X., Lao, X., Chen, M., Liu, R., Wei, Y., Ouyang, F., et al. (2016) PD-1hi Identifies a Novel Regulatory B-Cell Population in Human Hepatoma That Promotes Disease Progression. Cancer Discovery, 6, 546-559. [Google Scholar] [CrossRef] [PubMed]
[21] Wang, X., Wang, G., Wang, Z., Liu, B., Han, N., Li, J., et al. (2019) PD-1-Expressing B Cells Suppress CD4+ and CD8+ T Cells via PD-1/PD-L1-Dependent Pathway. Molecular Immunology, 109, 20-26. [Google Scholar] [CrossRef] [PubMed]
[22] Liu, M., Sun, Q., Wei, F. and Ren, X. (2020) Comprehensive Insights into the Effects and Regulatory Mechanisms of Immune Cells Expressing Programmed Death-1/programmed Death Ligand 1 in Solid Tumors. Cancer Biology and Medicine, 17, 626-639. [Google Scholar] [CrossRef] [PubMed]
[23] Gordon, S.R., Maute, R.L., Dulken, B.W., Hutter, G., George, B.M., McCracken, M.N., et al. (2017) PD-1 Expression by Tumour-Associated Macrophages Inhibits Phagocytosis and Tumour Immunity. Nature, 545, 495-499. [Google Scholar] [CrossRef] [PubMed]
[24] Zhou, D., Luan, J., Huang, C. and Li, J. (2021) Tumor-Associated Macrophages in Hepatocellular Carcinoma: Friend or Foe? Gut and Liver, 15, 500-516. [Google Scholar] [CrossRef] [PubMed]
[25] Park, D., Sung, P., Lee, G., Cho, S., Kim, S., Kang, B., et al. (2021) Preferential Expression of Programmed Death Ligand 1 Protein in Tumor-Associated Macrophages and Its Potential Role in Immunotherapy for Hepatocellular Carcinoma. International Journal of Molecular Sciences, 22, Article 4710. [Google Scholar] [CrossRef] [PubMed]
[26] Lu, C., Redd, P.S., Lee, J.R., Savage, N. and Liu, K. (2016) The Expression Profiles and Regulation of PD-L1 in Tumor-Induced Myeloid-Derived Suppressor Cells. OncoImmunology, 5, e1247135. [Google Scholar] [CrossRef] [PubMed]
[27] Liu, M., Wei, F., Wang, J., Yu, W., Shen, M., Liu, T., et al. (2021) Myeloid-Derived Suppressor Cells Regulate the Immunosuppressive Functions of PD-1PD-L1+ Bregs through PD-L1/PI3K/AKT/NF-κB Axis in Breast Cancer. Cell Death & Disease, 12, Article No. 465. [Google Scholar] [CrossRef] [PubMed]
[28] Nam, S., Lee, A., Lim, J. and Lim, J. (2019) Analysis of the Expression and Regulation of PD-1 Protein on the Surface of Myeloid-Derived Suppressor Cells (MDSCs). Biomolecules & Therapeutics, 27, 63-70. [Google Scholar] [CrossRef] [PubMed]
[29] Kuzume, A., Chi, S., Yamauchi, N. and Minami, Y. (2020) Immune-Checkpoint Blockade Therapy in Lymphoma. International Journal of Molecular Sciences, 21, Article 5456. [Google Scholar] [CrossRef] [PubMed]
[30] Callahan, M.K. and Wolchok, J.D. (2019) Recruit or Reboot? How Does Anti-PD-1 Therapy Change Tumor-Infiltrating Lymphocytes? Cancer Cell, 36, 215-217. [Google Scholar] [CrossRef] [PubMed]
[31] Kudo, M. (2019) Targeted and Immune Therapies for Hepatocellular Carcinoma: Predictions for 2019 and beyond. World Journal of Gastroenterology, 25, 789-807. [Google Scholar] [CrossRef] [PubMed]
[32] 国家卫生健康委办公厅. 原发性肝癌诊疗指南(2022年版) [J]. 临床肝胆病杂志, 2022, 38(2): 288-303.
[33] da Fonseca, L.G., Reig, M. and Bruix, J. (2020) Tyrosine Kinase Inhibitors and Hepatocellular Carcinoma. Clinics in Liver Disease, 24, 719-737. [Google Scholar] [CrossRef] [PubMed]
[34] Al-Salama, Z.T., Syed, Y.Y. and Scott, L.J. (2019) Lenvatinib: A Review in Hepatocellular Carcinoma. Drugs, 79, 665-674. [Google Scholar] [CrossRef] [PubMed]
[35] Liu, J., Tao, H., Yuan, T., Li, J., Li, J., Liang, H., et al. (2022) Immunomodulatory Effects of Regorafenib: Enhancing the Efficacy of Anti-PD-1/PD-L1 Therapy. Frontiers in Immunology, 13, Article 992611. [Google Scholar] [CrossRef] [PubMed]
[36] Wu, R., Kong, P., Xia, L., Huang, Y., Li, Z., Tang, Y., et al. (2019) Regorafenib Promotes Antitumor Immunity via Inhibiting PD-L1 and IDO1 Expression in Melanoma. Clinical Cancer Research, 25, 4530-4541. [Google Scholar] [CrossRef] [PubMed]
[37] Finn, R.S., Ikeda, M., Zhu, A.X., Sung, M.W., Baron, A.D., Kudo, M., et al. (2020) Phase Ib Study of Lenvatinib Plus Pembrolizumab in Patients with Unresectable Hepatocellular Carcinoma. Journal of Clinical Oncology, 38, 2960-2970. [Google Scholar] [CrossRef] [PubMed]
[38] Xu, J., Shen, J., Gu, S., Zhang, Y., Wu, L., Wu, J., et al. (2021) Camrelizumab in Combination with Apatinib in Patients with Advanced Hepatocellular Carcinoma (RESCUE): A Nonrandomized, Open-Label, Phase II Trial. Clinical Cancer Research, 27, 1003-1011. [Google Scholar] [CrossRef] [PubMed]
[39] Huang, C., Zhu, X., Shen, Y., Wu, D., Ji, Y., Ge, N., et al. (2021) Organ Specific Responses to First-Line Lenvatinib Plus Anti-PD-1 Antibodies in Patients with Unresectable Hepatocellular Carcinoma: A Retrospective Analysis. Biomarker Research, 9, Article No. 19. [Google Scholar] [CrossRef] [PubMed]
[40] Zhu, X., Huang, C., Shen, Y., Ji, Y., Ge, N., Qu, X., et al. (2021) Downstaging and Resection of Initially Unresectable Hepatocellular Carcinoma with Tyrosine Kinase Inhibitor and Anti-PD-1 Antibody Combinations. Liver Cancer, 10, 320-329. [Google Scholar] [CrossRef] [PubMed]
[41] Ho, W.J., Sharma, G., Zhu, Q., Stein-O’Brien, G., Durham, J., Anders, R., et al. (2020) Integrated Immunological Analysis of a Successful Conversion of Locally Advanced Hepatocellular Carcinoma to Resectability with Neoadjuvant Therapy. Journal for ImmunoTherapy of Cancer, 8, e000932. [Google Scholar] [CrossRef] [PubMed]
[42] Lee, W.S., Yang, H., Chon, H.J. and Kim, C. (2020) Combination of Anti-Angiogenic Therapy and Immune Checkpoint Blockade Normalizes Vascular-Immune Crosstalk to Potentiate Cancer Immunity. Experimental & Molecular Medicine, 52, 1475-1485. [Google Scholar] [CrossRef] [PubMed]
[43] Motz, G.T., Santoro, S.P., Wang, L., Garrabrant, T., Lastra, R.R., Hagemann, I.S., et al. (2014) Tumor Endothelium FasL Establishes a Selective Immune Barrier Promoting Tolerance in Tumors. Nature Medicine, 20, 607-615. [Google Scholar] [CrossRef] [PubMed]
[44] Kim, K., Park, S., Park, S.Y., Kim, G., Park, S.M., Cho, J., et al. (2020) Single-Cell Transcriptome Analysis Reveals TOX as a Promoting Factor for T Cell Exhaustion and a Predictor for Anti-PD-1 Responses in Human Cancer. Genome Medicine, 12, Article No. 22. [Google Scholar] [CrossRef] [PubMed]
[45] Nishino, M., Ramaiya, N.H., Chambers, E.S., Adeni, A.E., Hatabu, H., Jänne, P.A., et al. (2016) Immune-Related Response Assessment during PD-1 Inhibitor Therapy in Advanced Non-Small-Cell Lung Cancer Patients. Journal for ImmunoTherapy of Cancer, 4, 84. [Google Scholar] [CrossRef] [PubMed]
[46] Allen, E., Jabouille, A., Rivera, L.B., Lodewijckx, I., Missiaen, R., Steri, V., et al. (2017) Combined Antiangiogenic and Anti-PD-L1 Therapy Stimulates Tumor Immunity through HEV Formation. Science Translational Medicine, 9, eaak9679. [Google Scholar] [CrossRef] [PubMed]
[47] Shigeta, K., Matsui, A., Kikuchi, H., Klein, S., Mamessier, E., Chen, I.X., et al. (2020) Regorafenib Combined with PD1 Blockade Increases CD8 T-Cell Infiltration by Inducing CXCL10 Expression in Hepatocellular Carcinoma. Journal for ImmunoTherapy of Cancer, 8, e001435. [Google Scholar] [CrossRef] [PubMed]
[48] Deng, H., Kan, A., Lyu, N., Mu, L., Han, Y., Liu, L., et al. (2020) Dual Vascular Endothelial Growth Factor Receptor and Fibroblast Growth Factor Receptor Inhibition Elicits Antitumor Immunity and Enhances Programmed Cell Death-1 Checkpoint Blockade in Hepatocellular Carcinoma. Liver Cancer, 9, 338-357. [Google Scholar] [CrossRef] [PubMed]
[49] Esteban-Fabró, R., Willoughby, C.E., Piqué-Gili, M., Montironi, C., Abril-Fornaguera, J., Peix, J., et al. (2022) Cabozantinib Enhances Anti-Pd1 Activity and Elicits a Neutrophil-Based Immune Response in Hepatocellular Carcinoma. Clinical Cancer Research, 28, 2449-2460. [Google Scholar] [CrossRef] [PubMed]
[50] Cheng, A., Qin, S., Ikeda, M., Galle, P.R., Ducreux, M., Kim, T., et al. (2022) Updated Efficacy and Safety Data from Imbrave150: Atezolizumab plus Bevacizumab vs. Sorafenib for Unresectable Hepatocellular Carcinoma. Journal of Hepatology, 76, 862-873. [Google Scholar] [CrossRef] [PubMed]
[51] Ren, Z., Xu, J., Bai, Y., Xu, A., Cang, S., Du, C., et al. (2021) Sintilimab plus a Bevacizumab Biosimilar (IBI305) versus Sorafenib in Unresectable Hepatocellular Carcinoma (ORIENT-32): A Randomised, Open-Label, Phase 2-3 Study. The Lancet Oncology, 22, 977-990. [Google Scholar] [CrossRef] [PubMed]
[52] Wang, Y., Lu, L., Guan, Y., Ho, M., Lu, S., Spahn, J., et al. (2021) Atezolizumab plus Bevacizumab Combination Enables an Unresectable Hepatocellular Carcinoma Resectable and Links Immune Exclusion and Tumor Dedifferentiation to Acquired Resistance. Experimental Hematology & Oncology, 10, Article No. 45. [Google Scholar] [CrossRef] [PubMed]
[53] Hidaka, Y., Tomita, M., Desaki, R., Hamanoue, M., Takao, S., Kirishima, M., et al. (2022) Conversion Surgery for Hepatocellular Carcinoma with Portal Vein Tumor Thrombus after Successful Atezolizumab plus Bevacizumab Therapy: A Case Report. World Journal of Surgical Oncology, 20, Article No. 228. [Google Scholar] [CrossRef] [PubMed]
[54] Fife, B.T. and Bluestone, J.A. (2008) Control of Peripheral T‐Cell Tolerance and Autoimmunity via the CTLA‐4 and PD‐1 Pathways. Immunological Reviews, 224, 166-182. [Google Scholar] [CrossRef] [PubMed]
[55] Krummel, M.F. and Allison, J.P. (1995) CD28 and CTLA-4 Have Opposing Effects on the Response of T Cells to Stimulation. The Journal of Experimental Medicine, 182, 459-465. [Google Scholar] [CrossRef] [PubMed]
[56] Stamper, C.C., Zhang, Y., Tobin, J.F., Erbe, D.V., Ikemizu, S., Davis, S.J., et al. (2001) Crystal Structure of the B7-1/CTLA-4 Complex That Inhibits Human Immune Responses. Nature, 410, 608-611. [Google Scholar] [CrossRef] [PubMed]
[57] Yi, M., Zheng, X., Niu, M., Zhu, S., Ge, H. and Wu, K. (2022) Combination Strategies with PD-1/PD-L1 Blockade: Current Advances and Future Directions. Molecular Cancer, 21, Article No. 28. [Google Scholar] [CrossRef] [PubMed]
[58] Rotte, A. (2019) Combination of CTLA-4 and PD-1 Blockers for Treatment of Cancer. Journal of Experimental & Clinical Cancer Research, 38, Article No. 255. [Google Scholar] [CrossRef] [PubMed]
[59] Zhao, Y., Lee, C.K., Lin, C., Gassen, R.B., Xu, X., Huang, Z., et al. (2019) PD-L1:CD80 Cis-Heterodimer Triggers the Co-Stimulatory Receptor CD28 While Repressing the Inhibitory PD-1 and CTLA-4 Pathways. Immunity, 51, 1059-1073.e9. [Google Scholar] [CrossRef] [PubMed]
[60] Romano, E., Kusio-Kobialka, M., Foukas, P.G., Baumgaertner, P., Meyer, C., Ballabeni, P., et al. (2015) Ipilimumab-dependent Cell-Mediated Cytotoxicity of Regulatory T Cells Ex Vivo by Nonclassical Monocytes in Melanoma Patients. Proceedings of the National Academy of Sciences of the United States of America, 112, 6140-6145. [Google Scholar] [CrossRef] [PubMed]
[61] Saung, M.T., Pelosof, L., Casak, S., Donoghue, M., Lemery, S., Yuan, M., et al. (2021) FDA Approval Summary: Nivolumab plus Ipilimumab for the Treatment of Patients with Hepatocellular Carcinoma Previously Treated with Sorafenib. The Oncologist, 26, 797-806. [Google Scholar] [CrossRef] [PubMed]
[62] Martinez-Cannon, B.A., Castro-Sanchez, A., Barragan-Carrillo, R., de la Rosa Pacheco, S., Platas, A., Fonseca, A., et al. (2021) Adherence to Adjuvant Tamoxifen in Mexican Young Women with Breast Cancer. Patient Preference and Adherence, 15, 1039-1049. [Google Scholar] [CrossRef] [PubMed]
[63] Kelley, R.K., Sangro, B., Harris, W., Ikeda, M., Okusaka, T., Kang, Y., et al. (2021) Safety, Efficacy, and Pharmacodynamics of Tremelimumab plus Durvalumab for Patients with Unresectable Hepatocellular Carcinoma: Randomized Expansion of a Phase I/II Study. Journal of Clinical Oncology, 39, 2991-3001. [Google Scholar] [CrossRef] [PubMed]
[64] Shurin, M.R. and Umansky, V. (2022) Cross-Talk between HIF and PD-1/PD-L1 Pathways in Carcinogenesis and Therapy. Journal of Clinical Investigation, 132, e159473. [Google Scholar] [CrossRef] [PubMed]
[65] Bailey, C.M., Liu, Y., Liu, M., Du, X., Devenport, M., Zheng, P., et al. (2022) Targeting Hif-1α Abrogates Pd-L1-Mediated Immune Evasion in Tumor Microenvironment but Promotes Tolerance in Normal Tissues. Journal of Clinical Investigation, 132, e150846. [Google Scholar] [CrossRef] [PubMed]
[66] Zhu, Y., Chen, M., Xu, D., Li, T., Zhang, Z., Li, J., et al. (2022) The Combination of PD-1 Blockade with Interferon-α Has a Synergistic Effect on Hepatocellular Carcinoma. Cellular & Molecular Immunology, 19, 726-737. [Google Scholar] [CrossRef] [PubMed]
[67] Hu, B., Yu, M., Ma, X., Sun, J., Liu, C., Wang, C., et al. (2022) IFNα Potentiates Anti-Pd-1 Efficacy by Remodeling Glucose Metabolism in the Hepatocellular Carcinoma Microenvironment. Cancer Discovery, 12, 1718-1741. [Google Scholar] [CrossRef] [PubMed]
[68] Ru, J., Lu, J., Ge, J., Ding, B., Su, R., Jiang, Y., et al. (2024) IRGM Is a Novel Regulator of PD-L1 via Promoting S6k1-Mediated Phosphorylation of YBX1 in Hepatocellular Carcinoma. Cancer Letters, 581, Article ID: 216495. [Google Scholar] [CrossRef] [PubMed]
[69] Han, R., Ling, C., Wang, Y. and Lu, L. (2023) Enhancing HCC Treatment: Innovatively Combining HDAC2 Inhibitor with PD-1/PD-L1 Inhibition. Cancer Cell International, 23, Article No. 203. [Google Scholar] [CrossRef] [PubMed]
[70] Zhu, Y., Yang, J., Xu, D., Gao, X., Zhang, Z., Hsu, J.L., et al. (2019) Disruption of Tumour-Associated Macrophage Trafficking by the Osteopontin-Induced Colony-Stimulating Factor-1 Signalling Sensitises Hepatocellular Carcinoma to Anti-Pd-L1 Blockade. Gut, 68, 1653-1666. [Google Scholar] [CrossRef] [PubMed]
[71] Cai, M., Huang, W., Huang, J., Shi, W., Guo, Y., Liang, L., et al. (2022) Transarterial Chemoembolization Combined with Lenvatinib plus PD-1 Inhibitor for Advanced Hepatocellular Carcinoma: A Retrospective Cohort Study. Frontiers in Immunology, 13, Article 848387. [Google Scholar] [CrossRef] [PubMed]
[72] Wu, X., Yang, L., Chen, Y., Chen, Z., Lu, H., Shen, X., et al. (2024) Transcatheter Arterial Chemoembolisation Combined with Lenvatinib Plus Camrelizumab as Conversion Therapy for Unresectable Hepatocellular Carcinoma: A Single-Arm, Multicentre, Prospective Study. eClinicalMedicine, 67, Article ID: 102367. [Google Scholar] [CrossRef] [PubMed]
[73] Luo, X., Chang, R., Kuang, D., Yuan, M., Li, G., Zhang, B., et al. (2023) Case Report: Successful Conversion and Salvage Resection of Huge Hepatocellular Carcinoma with Portal Vein Tumor Thrombosis and Intrahepatic Metastasis via Sequential Hepatic Arterial Infusion Chemotherapy, Lenvatinib plus PD-1 Antibody Followed by Simultaneous Transcatheter Arterial Chemoembolization, and Portal Vein Embolization. Frontiers in Immunology, 14, Article 1285296. [Google Scholar] [CrossRef] [PubMed]
[74] He, M., Liang, R., Zhao, Y., Xu, Y., Chen, H., Zhou, Y., et al. (2021) Lenvatinib, Toripalimab, plus Hepatic Arterial Infusion Chemotherapy versus Lenvatinib Alone for Advanced Hepatocellular Carcinoma. Therapeutic Advances in Medical Oncology, 13, 8340-8359. [Google Scholar] [CrossRef] [PubMed]
[75] Chiang, C.L., Chiu, K.W.H., Chan, K.S.K., Lee, F.A.S., Li, J.C.B., Wan, C.W.S., et al. (2023) Sequential Transarterial Chemoembolisation and Stereotactic Body Radiotherapy Followed by Immunotherapy as Conversion Therapy for Patients with Locally Advanced, Unresectable Hepatocellular Carcinoma (START-FIT): A Single-Arm, Phase 2 Trial. The Lancet Gastroenterology & Hepatology, 8, 169-178. [Google Scholar] [CrossRef] [PubMed]
[76] Lurje, I., Czigany, Z., Bednarsch, J., Roderburg, C., Isfort, P., Neumann, U.P., et al. (2019) Treatment Strategies for Hepatocellular Carcinoma—A Multidisciplinary Approach. International Journal of Molecular Sciences, 20, Article 1465. [Google Scholar] [CrossRef] [PubMed]