Safety and Efficacy of Atezolizumab and Bevacizumab Combination as a First Line Treatment of Advanced Hepatocellular Carcinoma

被引:5
作者
Zanuso, Valentina [1 ,2 ]
Pirozzi, Angelo [1 ,2 ]
Balsano, Rita [2 ]
Pressiani, Tiziana [2 ]
Rimassa, Lorenza [1 ,2 ,3 ]
机构
[1] Humanitas Univ, Dept Biomed Sci, Milan, Italy
[2] IRCCS Humanitas Res Hosp, Med Oncol & Hematol Unit, Milan, Italy
[3] Humanitas Univ, Via Rita Levi Montalcini 4, I-20072 Milan, Italy
关键词
HCC; immune checkpoint inhibitors; atezolizumab; bevacizumab; safety; efficacy; PLUS BEVACIZUMAB; OPEN-LABEL; PHASE-III; 1ST-LINE TREATMENT; DOUBLE-BLIND; SORAFENIB; IMBRAVE150; LENVATINIB; OUTCOMES; ATEZO;
D O I
10.2147/JHC.S347932
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is one of the most common leading causes of cancer death worldwide. As most patients are diagnosed with advanced disease, systemic therapy remains the backbone of treatment. In recent years, we have witnessed the transformation of advanced HCC treatment landscapes from single-agent targeted therapies to immunotherapy combinations, with atezolizumab plus bevacizumab becoming the new first-line standard of care with an increase in overall survival, progression-free survival, and objective response rate compared to sorafenib, and a positive impact on quality of life. Although the efficacy and safety of this combination have been confirmed regardless of ethnicity, age, and etiology, only a subgroup of patients seems to benefit the most from this treatment. Currently, predictive serum and tissue biomarkers to select patients who are most likely to respond to atezolizumab plus bevacizumab are lacking. Moreover, the optimal subsequent therapy for patients who progress on first-line atezolizumab plus bevacizumab remains unknown, clinical trials are ongoing, and real-world data are needed to determine the most effective treatment sequence. Importantly, careful evaluation of bleeding risk and preservation of adequate liver function are fundamental to improve patients' prognosis, especially when subsequent treatments are administered.
引用
收藏
页码:1689 / 1708
页数:20
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