Dipasquale Angelo, Marinello Arianna, Santoro Armando
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, 20090, Italy.
IRCCS Humanitas Research Hospital, Rozzano, 20089, Italy.
J Hepatocell Carcinoma. 2021 Apr 15;8:241-251. doi: 10.2147/JHC.S270532. eCollection 2021.
Hepatocellular carcinoma (HCC) is the fifth most common malignancy across the world. Alongside improvement in local approaches for early stages, the prognosis of patients with advanced disease remains poor. The tyrosine kinase inhibitor sorafenib was the first drug approved for advanced HCC. During the past decade, this has been extensively explored in real-life settings, such as Eastern Cooperative Oncology Group performance status 2, Child-Pugh B liver function, chronic kidney disease, HIV infection, transplant recipients and the elderly. After 10 years, the multikinase inhibitor lenvatinib was approved in first-line setting. The Phase III REFLECT trial established the non-inferiority of lenvatinib compared with sorafenib in terms of overall survival, meanwhile exploratory analysis suggests a potential benefit over sorafenib for patients with HBV chronic infection and positive alpha-fetoprotein value. Experience with lenvatinib for patients not matching the REFLECT trial criteria remains promising but still retrospective. Indeed, the treatment sequence after lenvatinib still remains a crucial issue, considering that standard second-line options were tested only in patients who progressed to sorafenib. Overall, the choice between lenvatinib and sorafenib should take into account key selection criteria from randomized trials, evidence to date in special clinical situations, the physician's experience and patient's preference. Fast approval of atezolizumab plus bevacizumab as first-line treatment for advanced HCC brought an additional element in this scenario. Undoubtedly, lenvatinib and sorafenib remain available options for patients who are not suitable or those progressed to combination immunotherapy. It is conceivable that new systemic options will contribute to design a new treatment algorithm for HCC in the near future. Meanwhile, prospective studies and biomarker analysis are needed to help physicians in the choice between lenvatinib and sorafenib.
肝细胞癌(HCC)是全球第五大常见恶性肿瘤。随着早期阶段局部治疗方法的改进,晚期疾病患者的预后仍然很差。酪氨酸激酶抑制剂索拉非尼是首个被批准用于晚期HCC的药物。在过去十年中,该药已在现实环境中得到广泛探索,如东部肿瘤协作组体能状态评分为2、Child-Pugh B级肝功能、慢性肾病、HIV感染、移植受者以及老年人。十年后,多激酶抑制剂仑伐替尼被批准用于一线治疗。III期REFLECT试验证实仑伐替尼在总生存期方面不劣于索拉非尼,同时探索性分析表明,对于慢性乙肝感染且甲胎蛋白值为阳性的患者,仑伐替尼可能比索拉非尼更具优势。对于不符合REFLECT试验标准的患者,仑伐替尼的治疗经验仍很有前景,但仍属于回顾性研究。事实上,考虑到标准二线治疗方案仅在对索拉非尼治疗进展的患者中进行了测试,仑伐替尼之后的治疗顺序仍然是一个关键问题。总体而言,在仑伐替尼和索拉非尼之间做出选择应考虑随机试验的关键选择标准、特殊临床情况的现有证据、医生的经验以及患者的偏好。阿替利珠单抗联合贝伐单抗作为晚期HCC一线治疗的快速获批为这种情况增添了新的因素。毫无疑问,对于不适合或对联合免疫治疗进展的患者,仑伐替尼和索拉非尼仍然是可用的选择。可以想象,新的全身治疗方案将有助于在不久的将来设计出一种新的HCC治疗算法。同时,需要进行前瞻性研究和生物标志物分析,以帮助医生在仑伐替尼和索拉非尼之间做出选择。