Hilmi Marc, Vienot Angélique, Rousseau Benoît, Neuzillet Cindy
Department of Medical Oncology, Curie Institute, University of Versailles Saint-Quentin, 35 rue Dailly, 92210 Saint-Cloud, France.
GERCOR Group, 151 rue du Faubourg Saint-Antoine, 75011 Paris, France.
Cancers (Basel). 2019 Dec 27;12(1):77. doi: 10.3390/cancers12010077.
Hepatocellular carcinoma (HCC) and biliary tract cancers (BTC) display a poor prognosis with 5-year overall survival rates around 15%, all stages taken together. These primary liver malignancies are often diagnosed at advanced stages where therapeutic options are limited. Recently, immune therapy has opened new opportunities in oncology. Based on their high programmed death-ligand 1 expression and tumor-infiltrating lymphocytes, HCC and BTC are theoretically good candidates for immune checkpoint blockade. However, clinical activity of single agent immunotherapy appears limited to a subset of patients, which is still ill-defined, and combinations are under investigation. In this review, we provide an overview of (i) the biological rationale for immunotherapies in HCC and BTC, (ii) the current state of their clinical development, and (iii) the predictive value of immune signatures for both clinical outcome and response to these therapies.
肝细胞癌(HCC)和胆管癌(BTC)的预后较差,所有分期综合起来的5年总生存率约为15%。这些原发性肝脏恶性肿瘤往往在晚期才被诊断出来,此时治疗选择有限。最近,免疫疗法为肿瘤学带来了新的机遇。基于其高程序性死亡配体1表达和肿瘤浸润淋巴细胞,HCC和BTC理论上是免疫检查点阻断的良好候选者。然而,单药免疫疗法的临床活性似乎仅限于一部分患者,这部分患者仍不明确,目前正在研究联合疗法。在本综述中,我们概述了(i)HCC和BTC免疫疗法的生物学原理,(ii)其临床开发的现状,以及(iii)免疫特征对临床结果和这些疗法反应的预测价值。