为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Pathogenesis and Current Treatment Strategies of Hepatocellular Carcinoma.
Pathogenesis and Current Treatment Strategies of Hepatocellular Carcinoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
肝细胞癌(HCC)是最常见的肝癌,致死率高且五年生存率低,给全球医疗系统带来了沉重负担。HCC的发生和进展受多种病因危险因素促进,包括乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)感染、非酒精性/酒精性脂肪性肝病(N/AFLD)以及吸烟。在分子发病机制中,遗传学(TP53、TERT、CTNNB1等)、表观遗传学(DNA甲基化、miRNA、lncRNA等)的内源性改变以及关键信号通路(Wnt/β-catenin、JAK/STAT等)的失调强烈促进HCC的发生发展。多种不同病理机制的复杂多样性也反映了HCC个体化医学治疗的困难。HCC的治疗选择严格取决于肿瘤分期和肝功能,其依据更新的巴塞罗那临床肝癌分类系统进行分层。手术切除、局部消融技术和肝移植是早期肿瘤阶段有效且可治愈的治疗选择。对于多灶性和转移性疾病,推荐全身治疗。尽管索拉非尼数十年来一直是HCC唯一的一线治疗药物,但近期的进展使得新的一线及二线治疗选择获得批准。抗PD-L1导向的联合治疗,无论是与抗VEGF导向药物还是与抗CTLA-4活性物质联合,已成为一线治疗的新标准。
然而,临床试验数据表明,根据肝细胞癌的潜在发病机制,对特定治疗方案的应答存在差异。因此,当前国际临床指南除了采用增强横断面成像进行标准化影像学诊断外,还重新强调了组织病理学检查。在本综述中,我们着重阐述当前关于肝细胞癌分子发病机制的认识。借此机会,我们根据最近更新的巴塞罗那临床肝癌分类系统总结了早期和晚期肿瘤阶段的治疗序列,以及当前全身治疗算法(一线、二线和三线治疗)。
此外,我们讨论了新型预防性和治疗前方法,包括治疗性疫苗、过继性细胞转移、局部区域治疗增强以及基于非编码RNA的治疗作为有前景的治疗选择。这些新型治疗可能延长总生存率,同时兼顾生活质量和肝功能作为HCC治疗的支柱。
Hepatocellular carcinoma (HCC) is the most frequent liver cancer with high lethality and low five-year survival rates leading to a substantial worldwide burden for healthcare systems. HCC initiation and progression are favored by different etiological risk factors including hepatitis B virus (HBV) and hepatitis C virus (HCV) infection, non-/and alcoholic fatty liver disease (N/AFLD), and tobacco smoking. In molecular pathogenesis, endogenous alteration in genetics ( TP53 , TERT , CTNNB1 , etc.) , epigenetics (DNA-methylation, miRNA, lncRNA, etc.) , and dysregulation of key signaling pathways (Wnt/β-catenin, JAK/STAT, etc.) strongly contribute to the development of HCC. The multitude and complexity of different pathomechanisms also reflect the difficulties in tailored medical therapy of HCC.
Treatment options for HCC are strictly dependent on tumor staging and liver function, which are structured by the updated Barcelona Clinic Liver Cancer classification system. Surgical resection, local ablative techniques, and liver transplantation are valid and curative therapeutic options for early tumor stages. For multifocal and metastatic diseases, systemic therapy is recommended.
While Sorafenib had been the standalone HCC first-line therapy for decades, recent developments had led to the approval of new treatment options as first-line as well as second-line treatment. Anti-PD-L1 directed combination therapies either with anti-VEGF directed agents or with anti-CTLA-4 active substances have been implemented as the new treatment standard in the first-line setting.
However, data from clinical trials indicate different responses on specific therapeutic regimens depending on the underlying pathogenesis of hepatocellular cancer.
Therefore, histopathological examinations have been re-emphasized by current international clinical guidelines in addition to the standardized radiological diagnosis using contrast-enhanced cross-sectional imaging. In this review, we emphasize the current knowledge on molecular pathogenesis of hepatocellular carcinoma.
On this occasion, the treatment sequences for early and advanced tumor stages according to the recently updated Barcelona Clinic Liver Cancer classification system and the current algorithm of systemic therapy (first-, second-, and third-line treatment) are summarized.
Furthermore, we discuss novel precautional and pre-therapeutic approaches including therapeutic vaccination, adoptive cell transfer, locoregional therapy enhancement, and non-coding RNA-based therapy as promising treatment options. These novel treatments may prolong overall survival rates in regard with quality of life and liver function as mainstay of HCC therapy.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。