AGA Clinical Practice Guideline on Systemic Therapy for Hepatocellular Carcinoma

Background & Aims: Hepatocellular carcinoma (HCC), the most common primary liver cancer, remains a deadly cancer, with an incidence that has tripled in the United States since 1980. In recent years, new systemic therapies for HCC have been approved and a critical assessment of the existing data...

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Main Authors: Altayar, O. (Author), Estfan, B. (Author), Falck-Ytter, Y. (Author), O'Shea, R. (Author), Shah, R. (Author), Su, G.L (Author), Sultan, S. (Author), Wenzell, C. (Author)
Format: Article
Language:English
Published: W.B. Saunders 2022
Subjects:
Online Access:View Fulltext in Publisher
LEADER 03901nam a2200769Ia 4500
001 10-1053-j-gastro-2021-12-276
008 220420s2022 CNT 000 0 und d
020 |a 00165085 (ISSN) 
245 1 0 |a AGA Clinical Practice Guideline on Systemic Therapy for Hepatocellular Carcinoma 
260 0 |b W.B. Saunders  |c 2022 
300 |a 15 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1053/j.gastro.2021.12.276 
520 3 |a Background & Aims: Hepatocellular carcinoma (HCC), the most common primary liver cancer, remains a deadly cancer, with an incidence that has tripled in the United States since 1980. In recent years, new systemic therapies for HCC have been approved and a critical assessment of the existing data is necessary to balance benefits and harms and inform the development of evidence-based guidelines. Methods: The American Gastroenterological Association formed a multidisciplinary group consisting of a Technical Review Panel and a Guideline Panel. The Technical Review Panel prioritized clinical questions and outcomes according to their importance for clinicians and patients and conducted an evidence review of systemic therapies in patients with advanced-stage HCC. The Grading of Recommendations Assessment, Development and Evaluation framework was used to assess evidence. The Guideline Panel reviewed the evidence and used the Evidence-to-Decision Framework to develop recommendations. Results: The Panel reviewed the evidence, summarized in the Technical Review, for the following medications approved by the US Food and Drug Administration for HCC: first-line therapies: bevacizumab+atezolizumab, sorafenib, and lenvatinib; second-line therapies: cabozantinib, pembrolizumab, ramucirumab, and regorafenib; and other agents: bevacizumab, nivolumab, and nivolumab+ipilimumab. Conclusions: The Panel agreed on 11 recommendations focused on systemic therapy for HCC in patients who are not eligible for locoregional therapy or resection, those with metastatic disease and preserved liver function, those with poor liver function, and those on systemic therapy as adjuvant therapy. © 2022 
650 0 4 |a adjuvant chemotherapy 
650 0 4 |a anilide 
650 0 4 |a Anilides 
650 0 4 |a Antibodies, Monoclonal, Humanized 
650 0 4 |a antineoplastic agent 
650 0 4 |a Antineoplastic Agents 
650 0 4 |a Antineoplastic Combined Chemotherapy Protocols 
650 0 4 |a atezolizumab 
650 0 4 |a bevacizumab 
650 0 4 |a Bevacizumab 
650 0 4 |a cabozantinib 
650 0 4 |a carbanilamide derivative 
650 0 4 |a Carcinoma, Hepatocellular 
650 0 4 |a chemoembolization 
650 0 4 |a Chemoembolization, Therapeutic 
650 0 4 |a Chemotherapy, Adjuvant 
650 0 4 |a Hepatectomy 
650 0 4 |a Hepatocellular Carcinoma 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a lenvatinib 
650 0 4 |a Liver Cancer 
650 0 4 |a liver cell carcinoma 
650 0 4 |a Liver Neoplasms 
650 0 4 |a liver resection 
650 0 4 |a liver transplantation 
650 0 4 |a Liver Transplantation 
650 0 4 |a liver tumor 
650 0 4 |a monoclonal antibody 
650 0 4 |a pathology 
650 0 4 |a pathophysiology 
650 0 4 |a pembrolizumab 
650 0 4 |a Phenylurea Compounds 
650 0 4 |a practice guideline 
650 0 4 |a pyridine derivative 
650 0 4 |a Pyridines 
650 0 4 |a quinoline derivative 
650 0 4 |a Quinolines 
650 0 4 |a ramucirumab 
650 0 4 |a regorafenib 
650 0 4 |a retreatment 
650 0 4 |a Retreatment 
650 0 4 |a sorafenib 
650 0 4 |a Sorafenib 
650 0 4 |a Systemic Therapy 
700 1 0 |a Altayar, O.  |e author 
700 1 0 |a Estfan, B.  |e author 
700 1 0 |a Falck-Ytter, Y.  |e author 
700 1 0 |a O'Shea, R.  |e author 
700 1 0 |a Shah, R.  |e author 
700 1 0 |a Su, G.L.  |e author 
700 1 0 |a Sultan, S.  |e author 
700 1 0 |a Wenzell, C.  |e author 
773 |t Gastroenterology