Real-World Use of Immunotherapy for Hepatocellular Carcinoma.

IF 2.3 Q2 MEDICINE, GENERAL & INTERNAL Pragmatic and Observational Research Pub Date : 2023-08-21 eCollection Date: 2023-01-01 DOI:10.2147/POR.S397972
Amir Sara, Samantha M Ruff, Anne M Noonan, Timothy M Pawlik
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Abstract

Hepatocellular carcinoma (HCC) is the third most common cause of cancer-related mortality worldwide and accounts for 90% of all primary liver cancers. Chronic inflammation is the hallmark across most prevalent etiologies among which HBV is the leading cause worldwide (33%), followed by alcohol (30%), HCV (21%), other factors like non-alcoholic steatohepatitis linked to insulin resistance/metabolic syndrome, and obesity associated inflammation (16%). Deregulation of the tightly controlled immunological network leads to liver disease, including chronic infection, autoimmunity, and tumor development. While inflammation drives oncogenesis in the liver, HCC also recruits ICOS+ FOXP3+ Tregs and MDSCs and upregulates immune checkpoints to induce a state of immunosuppression in the tumor microenvironment. As such, research is focused on targeting and modulating the immune system to treat HCC. The Checkmate 040 and Keynote 224 studies established the role of immunotherapy in the treatment of patients with HCC. In Phase I and II trials, nivolumab and pembrolizumab demonstrated durable response rates of 15-20% and were subsequently approved as second-line agents after sorafenib. Due to the success of the IMbrave 150 and HIMALAYA trials, which examined the combination of atezolizumab/bevacizumab and tremelimumab/durvalumab, respectively, the FDA approved these regimens as first-time treatment options for patients with advanced HCC. The encouraging results of immunotherapy in the management of HCC has led researchers to evaluate if combination with locoregional therapies may result in a synergistic effect. Real-world studies represent an invaluable tool to assess and verify the applicability of clinical trials in the bedside setting with a more varied patient population. We herein review current real-life use of ICIs in the management of HCC and highlight some of the ongoing clinical trials that are expected to change current recommended first-line treatment in the near future.

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肝细胞癌免疫疗法的实际应用。
肝细胞癌(HCC)是全球第三大最常见的癌症相关死因,占所有原发性肝癌的 90%。慢性炎症是最常见的病因,其中 HBV 是全球最主要的病因(33%),其次是酒精(30%)、HCV(21%)、与胰岛素抵抗/代谢综合征相关的非酒精性脂肪性肝炎等其他因素以及肥胖相关炎症(16%)。严密控制的免疫网络失调会导致肝病,包括慢性感染、自身免疫和肿瘤发生。在炎症驱动肝脏肿瘤发生的同时,HCC 还会招募 ICOS+ FOXP3+ Tregs 和 MDSCs,并上调免疫检查点以诱导肿瘤微环境中的免疫抑制状态。因此,研究重点是针对和调节免疫系统来治疗 HCC。Checkmate 040 和 Keynote 224 研究确立了免疫疗法在治疗 HCC 患者中的作用。在I期和II期试验中,nivolumab和pembrolizumab的持久应答率达到15%-20%,随后被批准作为索拉非尼之后的二线药物。IMbrave 150 和 HIMALAYA 试验分别对 atezolizumab/bevacizumab 和 tremelimumab/durvalumab 的组合进行了研究,由于这两项试验的成功,FDA 批准将这些方案作为晚期 HCC 患者的首次治疗方案。免疫疗法在治疗 HCC 方面取得的令人鼓舞的成果促使研究人员开始评估与局部治疗相结合是否会产生协同效应。真实世界研究是一种宝贵的工具,可用于评估和验证临床试验在床边环境中对更多患者人群的适用性。我们在此回顾了 ICIs 目前在 HCC 治疗中的实际应用情况,并重点介绍了一些正在进行的临床试验,这些试验有望在不久的将来改变目前推荐的一线治疗方案。
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Pragmatic and Observational Research
Pragmatic and Observational Research MEDICINE, GENERAL & INTERNAL-
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期刊介绍: Pragmatic and Observational Research is an international, peer-reviewed, open-access journal that publishes data from studies designed to closely reflect medical interventions in real-world clinical practice, providing insights beyond classical randomized controlled trials (RCTs). While RCTs maximize internal validity for cause-and-effect relationships, they often represent only specific patient groups. This journal aims to complement such studies by providing data that better mirrors real-world patients and the usage of medicines, thus informing guidelines and enhancing the applicability of research findings across diverse patient populations encountered in everyday clinical practice.
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