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Systemic Therapy for Advanced Hepatocellular Carcinoma: ASCO Guideline

医学 伦瓦提尼 阿替唑单抗 无容量 瑞戈非尼 催眠药 贝伐单抗 彭布罗利珠单抗 肝细胞癌 肿瘤科 内科学 人口 卡波扎尼布 索拉非尼 癌症 结直肠癌 化疗 免疫疗法 环境卫生
作者
John D. Gordan,Erin B. Kennedy,Ghassan K. Abou-Alfa,Muhammad Shaalan Beg,Steven Brower,Terence P. Gade,Laura W. Goff,Shilpi Singh Gupta,Jennifer File Guy,William P. Harris,Renuka Iyer,Ishmael Jaiyesimi,Minaxi Jhawer,Asha Karippot,Ahmed Kaseb,Robin Kate Kelley,Jennifer J. Knox,Jeremy S. Kortmansky,Andrea Leaf,William M. Remak,Rachna T. Shroff,Davendra Sohal,Tamar H. Taddei,Neeta K. Venepalli,Andrea Wilson,Andrew X. Zhu,Michal G. Rose
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:38 (36): 4317-4345 被引量:158
标识
DOI:10.1200/jco.20.02672
摘要

PURPOSE To develop an evidence-based clinical practice guideline to assist in clinical decision making for patients with advanced hepatocellular carcinoma (HCC). METHODS ASCO convened an Expert Panel to conduct a systematic review of published phase III randomized controlled trials (2007-2020) on systemic therapy for advanced HCC and provide recommended care options for this patient population. RESULTS Nine phase III randomized controlled trials met the inclusion criteria. RECOMMENDATIONS Atezolizumab + bevacizumab (atezo + bev) may be offered as first-line treatment of most patients with advanced HCC, Child-Pugh class A liver disease, Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0-1, and following management of esophageal varices, when present, according to institutional guidelines. Where there are contraindications to atezolizumab and/or bevacizumab, tyrosine kinase inhibitors sorafenib or lenvatinib may be offered as first-line treatment of patients with advanced HCC, Child-Pugh class A liver disease, and ECOG PS 0-1. Following first-line treatment with atezo + bev, and until better data are available, second-line therapy with a tyrosine kinase inhibitor may be recommended for appropriate candidates. Following first-line therapy with sorafenib or lenvatinib, second-line therapy options for appropriate candidates include cabozantinib, regorafenib for patients who previously tolerated sorafenib, or ramucirumab (for patients with α-fetoprotein ≥ 400 ng/mL), or atezo + bev where patients did not have access to this option as first-line therapy. Pembrolizumab or nivolumab are also reasonable options for appropriate patients following sorafenib or lenvatinib. Consideration of nivolumab + ipilimumab as an option for second-line therapy and third-line therapy is discussed. Further guidance on choosing between therapy options is included within the guideline. Additional information is available at www.asco.org/gastrointestinal-cancer-guidelines .
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