TY - JOUR
T1 - Systemic Therapy for Advanced Hepatocellular Carcinoma
T2 - ASCO Guideline Update
AU - Gordan, John D.
AU - Kennedy, Erin B.
AU - Abou-Alfa, Ghassan K.
AU - Beal, Eliza
AU - Finn, Richard S.
AU - Gade, Terence P.
AU - Goff, Laura
AU - Gupta, Shilpi
AU - Guy, Jennifer
AU - Hoang, Hang T.
AU - Iyer, Renuka
AU - Jaiyesimi, Ishmael
AU - Jhawer, Minaxi
AU - Karippot, Asha
AU - Kaseb, Ahmed O.
AU - Kelley, R. Kate
AU - Kortmansky, Jeremy
AU - Leaf, Andrea
AU - Remak, William M.
AU - Sohal, Davendra P.S.
AU - Taddei, Tamar H.
AU - Wilson Woods, Andrea
AU - Yarchoan, Mark
AU - Rose, Michal G.
N1 - Publisher Copyright:
© American Society of Clinical Oncology.
PY - 2024/5/20
Y1 - 2024/5/20
N2 - PURPOSETo update an evidence-based guideline to assist in clinical decision-making for patients with advanced hepatocellular carcinoma (HCC).METHODSASCO convened an Expert Panel to update the 2020 guideline on systemic therapy for HCC. The panel updated the systematic review to include randomized controlled trials (RCTs) published through October 2023 and updated recommendations.RESULTSTen new RCTs met the inclusion criteria and were added to the evidence base.RECOMMENDATIONSAtezolizumab + bevacizumab (atezo + bev) or durvalumab + tremelimumab (durva + treme) may be offered first-line for patients with advanced HCC, Child-Pugh class A liver disease, and Eastern Cooperative Oncology Group performance status 0-1. Where there are contraindications to these therapies, sorafenib, lenvatinib, or durvalumab may be offered first-line. Following first-line treatment with atezo + bev, second-line therapy with a tyrosine kinase inhibitor (TKI), ramucirumab (for patients with alpha-fetoprotein [AFP] ≥400 ng/mL), durva + treme, or nivolumab + ipilimumab (nivo + ipi) may be recommended for appropriate candidates. Following first-line therapy with durva + treme, second-line therapy with a TKI is recommended. Following first-line treatment with sorafenib or lenvatinib, second-line therapy options include cabozantinib, regorafenib for patients who previously tolerated sorafenib, ramucirumab (AFP ≥400 ng/mL), nivo + ipi, or durvalumab; atezo + bev or durva + treme may be considered for patients who did not have access to these therapies in the first-line setting, and do not have contraindications. Pembrolizumab or nivolumab are also options for appropriate patients following sorafenib or lenvatinib. Third-line therapy may be considered in Child-Pugh class A patients with good PS, using one of the agents listed previously that has a nonidentical mechanism of action with previously received therapy. A cautious approach to systemic therapy is recommended for patients with Child-Pugh class B advanced HCC. Further guidance on choosing between options is included within the guideline.Additional information is available at www.asco.org/gastrointestinal-cancer-guidelines.
AB - PURPOSETo update an evidence-based guideline to assist in clinical decision-making for patients with advanced hepatocellular carcinoma (HCC).METHODSASCO convened an Expert Panel to update the 2020 guideline on systemic therapy for HCC. The panel updated the systematic review to include randomized controlled trials (RCTs) published through October 2023 and updated recommendations.RESULTSTen new RCTs met the inclusion criteria and were added to the evidence base.RECOMMENDATIONSAtezolizumab + bevacizumab (atezo + bev) or durvalumab + tremelimumab (durva + treme) may be offered first-line for patients with advanced HCC, Child-Pugh class A liver disease, and Eastern Cooperative Oncology Group performance status 0-1. Where there are contraindications to these therapies, sorafenib, lenvatinib, or durvalumab may be offered first-line. Following first-line treatment with atezo + bev, second-line therapy with a tyrosine kinase inhibitor (TKI), ramucirumab (for patients with alpha-fetoprotein [AFP] ≥400 ng/mL), durva + treme, or nivolumab + ipilimumab (nivo + ipi) may be recommended for appropriate candidates. Following first-line therapy with durva + treme, second-line therapy with a TKI is recommended. Following first-line treatment with sorafenib or lenvatinib, second-line therapy options include cabozantinib, regorafenib for patients who previously tolerated sorafenib, ramucirumab (AFP ≥400 ng/mL), nivo + ipi, or durvalumab; atezo + bev or durva + treme may be considered for patients who did not have access to these therapies in the first-line setting, and do not have contraindications. Pembrolizumab or nivolumab are also options for appropriate patients following sorafenib or lenvatinib. Third-line therapy may be considered in Child-Pugh class A patients with good PS, using one of the agents listed previously that has a nonidentical mechanism of action with previously received therapy. A cautious approach to systemic therapy is recommended for patients with Child-Pugh class B advanced HCC. Further guidance on choosing between options is included within the guideline.Additional information is available at www.asco.org/gastrointestinal-cancer-guidelines.
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U2 - 10.1200/JCO.23.02745
DO - 10.1200/JCO.23.02745
M3 - Article
C2 - 38502889
AN - SCOPUS:85192772672
SN - 0732-183X
VL - 42
SP - 1830
EP - 1850
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 15
ER -