Impact of older age in patients receiving atezolizumab and bevacizumab for hepatocellular carcinoma.


Journal

Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857

Informations de publication

Date de publication:
11 2022
Historique:
revised: 01 08 2022
received: 24 06 2022
accepted: 09 08 2022
pubmed: 21 8 2022
medline: 28 9 2022
entrez: 20 8 2022
Statut: ppublish

Résumé

Combination atezolizumab/bevacizumab is the gold standard for first-line treatment of unresectable hepatocellular carcinoma (HCC). Our study investigated the efficacy and safety of combination therapy in older patients with HCC. 191 consecutive patients from eight centres receiving atezolizumab and bevacizumab were included. Overall survival (OS), progression-free survival (PFS), overall response rate (ORR) and disease control rate (DCR) defined by RECIST v1.1 were measured in older (age ≥ 65 years) and younger (age < 65 years) age patients. Treatment-related adverse events (trAEs) were evaluated. The elderly (n = 116) had higher rates of non-alcoholic fatty liver disease (19.8% vs. 2.7%; p < .001), presenting with smaller tumours (6.2 cm vs 7.9 cm, p = .02) with less portal vein thrombosis (31.9 vs. 54.7%, p = .002), with fewer patients presenting with BCLC-C stage disease (50.9 vs. 74.3%, p = .002). There was no significant difference in OS (median 14.9 vs. 15.1 months; HR 1.15, 95% CI 0.65-2.02 p = .63) and PFS (median 7.1 vs. 5.5 months; HR 1.11, 95% CI 0.54-1.92; p = .72) between older age and younger age. Older patients had similar ORR (27.6% vs. 20.0%; p = .27) and DCR (77.5% vs. 66.1%; p = .11) compared to younger patients. Atezolizumab-related (40.5% vs. 48.0%; p = .31) and bevacizumab-related (44.8% vs. 41.3%; p = .63) trAEs were comparable between groups. Rates of grade ≥3 trAEs and toxicity-related treatment discontinuation were similar between older and younger age patients. Patients 75 years and older had similar survival and safety outcomes compared to younger patients. Atezolizumab and bevacizumab therapy is associated with comparable efficacy and tolerability in older age patients with unresectable HCC.

Sections du résumé

BACKGROUND AND AIMS
Combination atezolizumab/bevacizumab is the gold standard for first-line treatment of unresectable hepatocellular carcinoma (HCC). Our study investigated the efficacy and safety of combination therapy in older patients with HCC.
METHODS
191 consecutive patients from eight centres receiving atezolizumab and bevacizumab were included. Overall survival (OS), progression-free survival (PFS), overall response rate (ORR) and disease control rate (DCR) defined by RECIST v1.1 were measured in older (age ≥ 65 years) and younger (age < 65 years) age patients. Treatment-related adverse events (trAEs) were evaluated.
RESULTS
The elderly (n = 116) had higher rates of non-alcoholic fatty liver disease (19.8% vs. 2.7%; p < .001), presenting with smaller tumours (6.2 cm vs 7.9 cm, p = .02) with less portal vein thrombosis (31.9 vs. 54.7%, p = .002), with fewer patients presenting with BCLC-C stage disease (50.9 vs. 74.3%, p = .002). There was no significant difference in OS (median 14.9 vs. 15.1 months; HR 1.15, 95% CI 0.65-2.02 p = .63) and PFS (median 7.1 vs. 5.5 months; HR 1.11, 95% CI 0.54-1.92; p = .72) between older age and younger age. Older patients had similar ORR (27.6% vs. 20.0%; p = .27) and DCR (77.5% vs. 66.1%; p = .11) compared to younger patients. Atezolizumab-related (40.5% vs. 48.0%; p = .31) and bevacizumab-related (44.8% vs. 41.3%; p = .63) trAEs were comparable between groups. Rates of grade ≥3 trAEs and toxicity-related treatment discontinuation were similar between older and younger age patients. Patients 75 years and older had similar survival and safety outcomes compared to younger patients.
CONCLUSIONS
Atezolizumab and bevacizumab therapy is associated with comparable efficacy and tolerability in older age patients with unresectable HCC.

Identifiants

pubmed: 35986902
doi: 10.1111/liv.15405
pmc: PMC9825835
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Bevacizumab 2S9ZZM9Q9V
atezolizumab 52CMI0WC3Y

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2538-2547

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Cancer Research UK
ID : RCCPDB-NOV21/100008
Pays : United Kingdom
Organisme : Wellcome Trust
ID : PS3416
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2022 The Authors. Liver International published by John Wiley & Sons Ltd.

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Auteurs

Mathew Vithayathil (M)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.

Antonio D'Alessio (A)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.

Claudia A M Fulgenzi (CAM)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Division of Medical Oncology, Policlinico Universitario Campus Bio-Medico, Rome, Italy.

Naoshi Nishida (N)

Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan.

Martin Schönlein (M)

Department of Oncology, Hematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Johann von Felden (J)

Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Kornelius Schulze (K)

Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Henning Wege (H)

Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Anwaar Saeed (A)

Division of Medical Oncology, Department of Medicine, Kansas University Cancer Center, Kansas City, Kansas, USA.

Brooke Wietharn (B)

Division of Medical Oncology, Department of Medicine, Kansas University Cancer Center, Kansas City, Kansas, USA.

Hannah Hildebrand (H)

Division of Medical Oncology, Department of Medicine, Kansas University Cancer Center, Kansas City, Kansas, USA.

Linda Wu (L)

Division of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute, Mount Sinai Hospital, New York, New York, USA.

Celina Ang (C)

Division of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute, Mount Sinai Hospital, New York, New York, USA.

Thomas U Marron (TU)

Division of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute, Mount Sinai Hospital, New York, New York, USA.

Arndt Weinmann (A)

I. Medical Department, University Medical Center Mainz, Mainz, Germany.

Peter R Galle (PR)

I. Medical Department, University Medical Center Mainz, Mainz, Germany.

Dominik Bettinger (D)

Department of Medicine II (Gastroenterology, Hepatology, Endocrinology and Infectious Diseases), Faculty of Medicine, Freiburg University Medical Center, University of Freiburg, Freiburg, Germany.

Bertram Bengsch (B)

Department of Medicine II (Gastroenterology, Hepatology, Endocrinology and Infectious Diseases), Faculty of Medicine, Freiburg University Medical Center, University of Freiburg, Freiburg, Germany.
University of Freiburg, Signalling Research Centers BIOSS and CIBSS, Freiburg, Germany.
German Cancer Consortium (DKTK), Partner Site, Freiburg, Germany.

Arndt Vogel (A)

Hannover Medical School, Hannover, Germany.

Lorenz Balcar (L)

Division of Gastroenterology & Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

Bernhard Scheiner (B)

Division of Gastroenterology & Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

Pei-Chang Lee (PC)

Division of Gastroenterology and Hepatology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.

Yi-Hsiang Huang (YH)

Division of Gastroenterology and Hepatology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Institute of Clinical Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

Suneetha Amara (S)

Division of Hematology/Oncology, East Carolina University, Greenville, North Carolina, USA.

Mahvish Muzaffar (M)

Division of Hematology/Oncology, East Carolina University, Greenville, North Carolina, USA.

Abdul Rafeh Naqash (AR)

Division of Hematology/Oncology, East Carolina University, Greenville, North Carolina, USA.
Medical Oncology/TSET Phase 1 Program, Stephenson Cancer Center, University of Oklahoma, Norman, Oklahoma, USA.

Antonella Cammarota (A)

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Italy.

Nicola Personeni (N)

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Italy.

Tiziana Pressiani (T)

Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Italy.

Matthias Pinter (M)

Division of Gastroenterology & Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

Alessio Cortellini (A)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.

Masatoshi Kudo (M)

Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan.

Lorenza Rimassa (L)

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Italy.

David J Pinato (DJ)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Division of Oncology, Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy.

Rohini Sharma (R)

Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.

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