医学
索拉非尼
全身疗法
重症监护医学
伦瓦提尼
肿瘤科
阿替唑单抗
贝伐单抗
瑞戈非尼
杜瓦卢马布
疾病
无容量
内科学
彭布罗利珠单抗
免疫疗法
癌症
肝细胞癌
化疗
乳腺癌
结直肠癌
作者
Valentina Zanuso,Lorenza Rimassa,Chiara Braconi
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2023-09-11
被引量:3
标识
DOI:10.1097/hep.0000000000000572
摘要
Over the past years, there has been a remarkable advance in the systemic treatment options for advanced HCC. The overall survival has gradually increased over time, with larger benefits for patients with sensitive tumors and preserved liver function, the latter being an essential condition for the delivery of sequential lines of treatment and optimization of clinical outcomes. With the approval of new first-line agents and the introduction of immune checkpoint inhibitor-based therapies, the treatment landscape of advanced HCC is becoming wider than ever. Atezolizumab plus bevacizumab and, more recently, durvalumab plus tremelimumab have entered the clinical practice and are the current standard of care for treatment-naïve patients, surpassing sorafenib and lenvatinib monopoly. As no head-to-head comparisons are available among all the first-line treatment options, the recommendation for the most appropriate choice and sequence is patient-driven and integrates efficacy data with clinical comorbidities, background liver disease, and the safety profile of available drugs. In addition, predictive biomarkers for successful patients’ stratification are yet to be available and constitute the focus of ongoing research. The treatment algorithm is likely to become even more complex since systemic therapeutic approaches are now being translated into earlier stages of the disease, with an impact on the evolution of the sequential treatment of patients with HCC.
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