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Preliminary evidence of safety and tolerability of atezolizumab plus bevacizumab in patients with hepatocellular carcinoma and Child-Pugh A and B cirrhosis: A real-world study.

Authors :
D'Alessio A
Fulgenzi CAM
Nishida N
Schönlein M
von Felden J
Schulze K
Wege H
Gaillard VE
Saeed A
Wietharn B
Hildebrand H
Wu L
Ang C
Marron TU
Weinmann A
Galle PR
Bettinger D
Bengsch B
Vogel A
Balcar L
Scheiner B
Lee PC
Huang YH
Amara S
Muzaffar M
Naqash AR
Cammarota A
Personeni N
Pressiani T
Sharma R
Pinter M
Cortellini A
Kudo M
Rimassa L
Pinato DJ
Source :
Hepatology (Baltimore, Md.) [Hepatology] 2022 Oct; Vol. 76 (4), pp. 1000-1012. Date of Electronic Publication: 2022 Apr 08.
Publication Year :
2022

Abstract

Background and Aims: Atezolizumab plus bevacizumab (AtezoBev) is the standard of care for first-line treatment of unresectable HCC. No evidence exists as to its use in routine clinical practice in patients with impaired liver function.<br />Approach and Results: In 216 patients with HCC who were consecutively treated with AtezoBev across 11 tertiary centers, we retrospectively evaluated treatment-related adverse events (trAEs) graded (G) according to Common Terminology Criteria for Adverse Events v5.0, including in the analysis all patients treated according to label (n = 202, 94%). We also assessed overall survival (OS), progression-free survival (PFS), overall response (ORR), and disease control rates (DCR) defined by Response Evaluation Criteria in Solid Tumors v1.1. Disease was mostly secondary to viral hepatitis, namely hepatitis C (n = 72; 36%) and hepatitis B infection (n = 35, 17%). Liver function was graded as Child-Pugh (CP)-A in 154 patients (76%) and CP-B in 48 (24%). Any grade trAEs were reported by 143 patients (71%), of which 53 (26%) were G3 and 3 (2%) G4. Compared with CP-A, patients with CP-B showed comparable rates of trAEs. Presence and grade of varices at pretreatment esophagogastroduodenoscopy did not correlate with bleeding events. After a median follow-up of 9.0 months (95% CI, 7.8-10.1), median OS was 14.9 months (95% CI, 13.6-16.3), whereas median PFS was 6.8 months (95% CI, 5.2-8.5). ORR and DCR were respectively 25% and 73%, with no difference across CP classes.<br />Conclusions: This study confirms reproducible safety and efficacy of AtezoBev in routine practice. Patients with CP-B reported similar tolerability compared with CP-A, warranting prospective evaluation of AtezoBev in this treatment-deprived population.<br /> (© 2022 The Authors. Hepatology published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases.)

Details

Language :
English
ISSN :
1527-3350
Volume :
76
Issue :
4
Database :
MEDLINE
Journal :
Hepatology (Baltimore, Md.)
Publication Type :
Academic Journal
Accession number :
35313048
Full Text :
https://doi.org/10.1002/hep.32468