Real-World Outcomes of Atezolizumab with Bevacizumab Treatment in Hepatocellular Carcinoma Patients: Effectiveness, Esophagogastroduodenoscopy Utilization and Bleeding Complications

Author:

Lee Cha1ORCID,Freeman Mark2,Burak Kelly3ORCID,Moffat Gordon1,O’Donnell Conor4,Ding Philip2ORCID,Lyubetska Hanna5,Meyers Brandon4,Gordon Vallerie5,Kosyachkova Ekaterina1,Bucur Roxana1,Cheung Winson2,Knox Jennifer1,Tam Vincent2

Affiliation:

1. Princess Margaret Cancer Center, University of Toronto, Toronto, ON M5G1Z5, Canada

2. Tom Baker Cancer Center, University of Calgary, Calgary, AB T2N4N2, Canada

3. Liver Unit, Divisions of Gastroenterology & Hepatology and Transplant Medicine, Departments of Medicine and Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N4N2, Canada

4. Juravinski Cancer Center, Escarpment Cancer Research Institute, McMaster University, Hamilton, ON L8S4L8, Canada

5. CancerCare Manitoba, University of Manitoba, Winnipeg, MB R3A1R9, Canada

Abstract

The IMbrave150 trial established atezolizumab with bevacizumab (A+B) as standard care for hepatocellular carcinoma (HCC), recommending an esophagogastroduodenoscopy (EGD) within 6 months of treatment initiation to prevent bleeding from esophagogastric varices. The necessity of mandatory EGD for all patients remains unclear. We retrospectively analyzed 112 HCC patients treated with A+B at five Canadian cancer centers from 1 July 2020 to 31 August 2022. A+B was the first-line therapy for 90% of patients, with median overall survival at 20.3 months and progression-free survival at 9.6 months. There was no survival difference between patients with bleeding and those without. Before A+B, 71% (n = 79) of patients underwent an EGD within 6 months, revealing varices in 41% (n = 32) and requiring intervention in 19% (n = 15). The overall bleeding rate was 15% (n = 17), with GI-specific bleeding occurring in 5% (n = 17). In the EGD group, GI-specific bleeding was 6% (n = 5) while in the non-EGD group, it was 3% (n = 1). Non-GI bleeding was observed in 10% (n = 11) of patients. Outcomes for HCC patients treated with A+B in Canada were comparable to IMbrave150. There was no increase in GI bleeding in patients without pre-treatment EGD, possibly supporting a selective EGD approach.

Publisher

MDPI AG

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