Efficacy and safety of atezolizumab/bevacizumab in patients with HCC after prior systemic therapy: A global, observational study
Year: 2023
Type: article
Study design: Observational Study
Abstract: BACKGROUND: Since the introduction of the combination treatment of anti-programmed death-ligand 1 antibody atezolizumab and anti-VEGF antibody bevacizumab (AB), median overall survival in HCC has drastically improved. However, evidence on the efficacy and safety of the novel treatment standard in patients with prior exposure to systemic treatment is scarce. The aim of this global, multicenter, observational study was to evaluate the efficacy and safety of AB in patients after previous systemic therapy. METHODS: We screened our global, multicenter, prospectively maintained registry database for patients who received any systemic therapy before AB. The primary end point was overall survival; secondary end points were time-to-progression, progression-free survival, objective response rate, and safety (rate and severity of adverse events). RESULTS: Among 493 patients who received AB for unresectable HCC, 61 patients received prior systemic therapy and were included in this analysis. The median age of the study population was 66 years, with 91.8% males. Predominant risk factors for HCC were viral hepatitis (59%) and alcohol (23%). Overall survival for AB was 16.2 (95% CI, 14.5-17.9) months, time-to-progression and progression-free survival were 4.1 (95% CI, 1.5-6.6) and 3.1 (95% CI, 1.1-5.1) months, respectively. The objective response rate was 38.2% (7.3% with complete and 30.9% with partial response). Overall survival was not influenced by treatment line (2nd vs. >2nd) or previous systemic treatment modality (tyrosine kinase inhibitors vs. immune checkpoint inhibitors). Treatment-related adverse events of all grades according to Common Terminology Criteria for Adverse Events were documented in 42.6% of patients, with only 13.1% of grade ≥3, including one death. CONCLUSION: In this observational study, AB emerges as a safe and efficacious treatment option in patients with HCC previously treated with other systemic therapy.
Source: Hepatology Communications
Authors: Vincent Joerg, Bernhard Scheiner, Antonio D´Alessio, Claudia A.M. Fulgenzi, Martin Schönlein, Lorenz Kocheise, Ansgar W. Lohse, Samuel Huber, Henning Wege, Ahmed Kaseb, Yinghong Wang, Antony Mathew, Andrew Kuang, Mahvish Muzaffar, Yehia I. Abugabal, Shadi Chamseddine, Samuel Phen, Jaekyung Cheon, Pei-Chang Lee, Lorenz Balcar, Anja Krall, Celina Ang, Linda Wu, Anwaar Saeed, Yi-Hsiang Huang, Bertram Bengsch, Lorenza Rimassa, Arndt Weinmann, Rudolf Stauber, James Korolewicz, Matthias Pinter, Amit G. Singal, Hong Jae Chon, David J. Pinato, Kornelius Schulze, Johann von Felden
Institutions: University Medical Center Hamburg-Eppendorf, Imperial College London, Medical University of Vienna, Campus Bio Medico University Hospital, The University of Texas MD Anderson Cancer Center, The University of Texas Health Science Center at Houston, Baylor College of Medicine, East Carolina University, The University of Texas Southwestern Medical Center, CHA University Bundang Medical Center, CHA University, Taipei Veterans General Hospital, Medical University of Graz, Mount Sinai Hospital, Tisch Cancer Institute, University of Pittsburgh, UPMC Health System, University of Pittsburgh Medical Center, National Yang Ming Chiao Tung University, University of Freiburg, University Medical Center Freiburg, Deutsches Konsortium für Translationale Krebsforschung, Humanitas University, IRCCS Humanitas Research Hospital, Johannes Gutenberg University Mainz, University Medical Center of the Johannes Gutenberg University Mainz, Università degli Studi del Piemonte Orientale “Amedeo Avogadro”
Language: English
Subfield: Hepatology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,700
Funders: Falk Foundation, Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, Gilead Sciences, FibroGen, Wilhelm Sander-Stiftung, Exelixis, ViiV Healthcare, Agios Pharmaceuticals, BeiGene, Incyte, Innovent Biologics, Actuate Therapeutics, Cancer Research UK, National Institute for Health and Care Research, Bayer HealthCare, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Eisai, Deutsche Krebshilfe, European Association for the Study of the Liver, Servier, Ipsen, LEO Pharma, National Institutes of Health, Genentech, National Cancer Institute, National Institute on Minority Health and Health Disparities, Daiichi Sankyo Europe
OpenAlex ID: W4387965246
