ASCO GUIDELINES Bundle

Hepatocellular Carcinoma Pocket Guide - 2021

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Key Points ➤ HCC is the fourth leading cause of cancer deaths worldwide, accounting for approximately 670,000 new cases and 625,000 deaths in 2018. ➤ Atezolizumab + bevacizumab (atezo + bev) may be offered as first-line treatment for most patients with advanced HCC, following management of esophageal varices, when present. ➤ Second-line therapy with a tyrosine kinase inhibitor may be recommended for appropriate candidates. Treatment First-Line Therapy ➤ Recommendation 1.1: Atezolizumab-bevacizumab (atezo + bev) may be offered as first-line treatment for most patients with advanced HCC, Child-Pugh class A, ECOG PS 0-1, and following management of esophageal varices, when present, according to institutional guidelines (Strong recommendation; EB-B-M/H). Qualifying statements: ▶ Recommendation 1.1 is based on results from the IMbrave150 phase III RCT comparison of atezo + bev to sorafenib (HR for OS, 0.58; 95% CI, 0.42 to 0.79; P = 0.0006) in Child- Pugh class A patients. Caution should be exercised when applying these results to patients with more advanced liver disease who have a greater likelihood of portal hypertension because of the risk of bleeding complications associated with bevacizumab. ▶ Due to risk of bleeding, patients in this trial were required to have undergone esophagogastroduodenoscopy (EGD) within 6 months of trial initiation and to have received treatment of esophageal varices when necessary. The Expert Panel recognizes that some patients may have been evaluated for varices outside the 6-month window, are receiving treatment (eg, adequately dosed nonselective β-blockers), and/or are deemed to be low risk for variceal bleed by a hepatolog y specialist. In these patients, the decision to forgo an EGD prior to initiation of therapy with atezo + bev may be carefully considered. ▶ Patients who had a myocardial infarction or stroke within the previous 3 months, had a history of autoimmune disease, were on therapeutic anticoagulation, or had coinfection with HBV and HCV were also excluded from the IMbrave150 RCT.

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