Boilève Alice, Hilmi Marc, Delaye Matthieu, Tijeras-Raballand Annemilaï, Neuzillet Cindy
Gustave Roussy, Département de Médecine Oncologique, 94805 Villejuif, France.
GERCOR Group, 151 rue du Faubourg Saint-Antoine, 75011 Paris, France.
Cancers (Basel). 2021 May 30;13(11):2708. doi: 10.3390/cancers13112708.
Hepatocellular carcinoma (HCC) and biliary tract cancers (BTC) exhibit a poor prognosis with 5-year overall survival rates around 15%, all stages combined. Most of these primary liver malignancies are metastatic at diagnostic, with only limited therapeutic options, relying mainly on systemic therapies. Treatment modalities are different yet partially overlapping between HCC and BTC. The complex molecular profile of BTC yields to several actionable therapeutic targets, contrary to HCC that remains the field of antiangiogenic drugs in non-molecularly selected patients. Immunotherapy is now validated in the first line in HCC in combination with bevacizumab, while clinical activity of single agent immunotherapy appears limited to a subset of patients in BTC, still poorly characterized, and combinations are currently under investigation. In this review, we provide a critical evaluation and grading of clinical relevance on (i) the main prognostic biomarkers in HCC and BTC, (ii) the main theragnostic biomarkers in both tumors, and lastly (iii) what is recommended in clinical practice.
肝细胞癌(HCC)和胆管癌(BTC)的预后较差,所有分期综合计算的5年总生存率约为15%。这些原发性肝癌大多在诊断时已发生转移,治疗选择有限,主要依赖全身治疗。HCC和BTC的治疗方式不同但部分重叠。与HCC不同,BTC复杂的分子特征产生了几个可操作的治疗靶点,在未进行分子选择的患者中,HCC仍是抗血管生成药物的应用领域。免疫疗法目前已在HCC一线治疗中与贝伐单抗联合得到验证,而单药免疫疗法的临床活性似乎仅限于BTC患者的一个亚组,该亚组特征仍不明确,目前正在研究联合治疗方案。在本综述中,我们对以下内容进行了关键评估和临床相关性分级:(i)HCC和BTC的主要预后生物标志物;(ii)两种肿瘤的主要治疗诊断生物标志物;最后(iii)临床实践中的推荐内容。