Suppr超能文献

血管生成和免疫检查点抑制剂作为肝细胞癌的治疗方法:当前的知识和未来的研究方向。

Angiogenesis and immune checkpoint inhibitors as therapies for hepatocellular carcinoma: current knowledge and future research directions.

机构信息

Department of Medical Oncology, Curie Institute, University of Versailles Saint-Quentin, Paris, France.

Department of Pathology, Henri Mondor Hospital, Créteil, France.

出版信息

J Immunother Cancer. 2019 Nov 29;7(1):333. doi: 10.1186/s40425-019-0824-5.

Abstract

Hepatocellular carcinoma (HCC) is the second deadliest cancer worldwide, due to its high incidence and poor prognosis. Frequent initial presentation at advanced stages along with impaired liver function limit the use of a broad therapeutic arsenal in patients with HCC. Although main HCC oncogenic drivers have been deciphered in recent years (TERT, TP53, CTNNB1 mutations, miR122 and CDKN2A silencing), therapeutic applications derived from this molecular knowledge are still limited. Given its high vascularization and immunogenicity, antiangiogenics and immune checkpoint inhibitors (ICI), respectively, are two therapeutic approaches that have shown efficacy in HCC. Depending on HCC immune profile, combinations of these therapies aim to modify the protumoral/antitumoral immune balance, and to reactivate and favor the intratumoral trafficking of cytotoxic T cells. Combination therapies involving antiangiogenics and ICI may be synergistic, because vascular endothelial growth factor A inhibition increases intratumoral infiltration and survival of cytotoxic T lymphocytes and decreases regulatory T lymphocyte recruitment, resulting in a more favorable immune microenvironment for ICI antitumoral activity. First results from clinical trials evaluating combinations of these therapies are encouraging with response rates never observed before in patients with HCC. A better understanding of the balance and interactions between protumoral and antitumoral immune cells will help to ensure the success of future therapeutic trials. Here, we present an overview of the current state of clinical development of antitumoral therapies in HCC and the biological rationale for their use. Moreover, translational studies on tumor tissue and blood, prior to and during treatment, will help to identify biomarkers and immune signatures with predictive value for both clinical outcome and response to combination therapies.

摘要

肝细胞癌 (HCC) 是全球第二大致命癌症,其发病率高且预后差。由于 HCC 常于早期进展期就诊,且伴有肝功能受损,限制了 HCC 患者广泛应用治疗方案。尽管近年来已经解析了 HCC 的主要致癌驱动因素(TERT、TP53、CTNNB1 突变、miR122 和 CDKN2A 沉默),但从这些分子知识衍生的治疗应用仍然有限。鉴于 HCC 的高血管生成和免疫原性,抗血管生成剂和免疫检查点抑制剂(ICI)分别是两种已在 HCC 中显示疗效的治疗方法。根据 HCC 的免疫特征,这些疗法的组合旨在改变促肿瘤/抗肿瘤免疫平衡,并重新激活和有利于细胞毒性 T 细胞在肿瘤内的迁移。抗血管生成剂和 ICI 的联合治疗可能具有协同作用,因为血管内皮生长因子 A 抑制增加了肿瘤内浸润和细胞毒性 T 淋巴细胞的存活率,并减少了调节性 T 淋巴细胞的募集,从而为 ICI 的抗肿瘤活性提供了更有利的免疫微环境。评估这些疗法联合应用的临床试验的初步结果令人鼓舞, HCC 患者的缓解率从未达到过如此高的水平。更好地了解促肿瘤和抗肿瘤免疫细胞之间的平衡和相互作用,将有助于确保未来治疗试验的成功。在这里,我们概述了 HCC 抗肿瘤治疗的临床开发现状及其应用的生物学依据。此外,在治疗前和治疗期间对肿瘤组织和血液进行转化研究,将有助于确定具有预测临床结果和联合治疗反应价值的生物标志物和免疫特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18b7/6884868/dabf2195f5b8/40425_2019_824_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验