Division of Hematology and Oncology, Loyola University Medical Center, Maywood, IL, USA.
Curr Gastroenterol Rep. 2022 May;24(5):65-71. doi: 10.1007/s11894-022-00842-9. Epub 2022 Apr 13.
Multiple new tyrosine kinase inhibitors, immunotherapies and anti-angiogenic therapies are now available for the treatment of advanced hepatocellular carcinoma (HCC). In this article, we reviewed the evidence supporting these new therapies.
The combination of atezolizumab and bevacizumab has become a new standard of care for initial systemic therapy in eligible patients, replacing sorafenib in the first line for many patients. Lenvatinib, a multikinase inhibitor, is also a new first line treatment option for patients who are not eligible for immunotherapy. Several additional options for second line treatment were also reviewed in detail in this paper. New systemic therapies for advanced HCC have prolonged overall survival. However, these new therapies are primarily approved for patients with Child-Pugh A classification with few options for patients with Child-Pugh B disease. Further work is needed to expand options for patients with more advanced liver disease and to optimize the sequencing of these new therapies.
目前有多种新型酪氨酸激酶抑制剂、免疫疗法和抗血管生成疗法可用于治疗晚期肝细胞癌(HCC)。本文回顾了支持这些新疗法的证据。
阿替利珠单抗联合贝伐珠单抗已成为适合患者初始系统治疗的新标准,在许多患者中取代了索拉非尼作为一线治疗药物。仑伐替尼是一种多激酶抑制剂,也是不适合免疫治疗患者的新一线治疗选择。本文还详细回顾了二线治疗的其他几种选择。晚期 HCC 的新系统疗法延长了总生存期。然而,这些新疗法主要批准用于 Child-Pugh A 分级的患者,Child-Pugh B 级疾病患者的选择有限。需要进一步研究以扩大对更晚期肝病患者的选择,并优化这些新疗法的序贯治疗。