Evidence map›Paper›PMID 40677696›Full record

ArticleJHEP reports : innovation in hepatology2025

Efficacy of atezolizumab plus bevacizumab for unresectable HCC: Systematic review and meta-analysis of real-world evidence.

Giulia Francesca Manfredi, Claudia Angela Maria Fulgenzi, Ciro Celsa, Bernardo Stefanini, Antonio D'Alessio, Matthias Pinter, Bernhard Scheiner, Nichola Awosika, Leonardo Brunetti, Pasquale Lombardi and 17 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Giulia Francesca ManfrediDepartment of Translational Medicine, Università del Piemonte Orientale, Novara, Italy.
Claudia Angela Maria FulgenziDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Ciro CelsaDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Bernardo StefaniniDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Antonio D'AlessioDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Matthias PinterDivision of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
Bernhard ScheinerDivision of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
Nichola AwosikaDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Leonardo BrunettiDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Pasquale LombardiDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Charles LatchfordDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Pei-Chang LeeDivision of Gastroenterology and Hepatology, Taipei Veterans General Hospital, Taipei, Taiwan.
Yi-Hsiang HuangDivision of Gastroenterology and Hepatology, Taipei Veterans General Hospital, Taipei, Taiwan.
Chun-Yen LinDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan, Taiwan.
Andrea DalbeniGeneral Medicine C & Liver Unit, Medicine Department, University of Verona and University and Hospital Trust (AOUI) of Verona, Verona, Italy.
Arndt VogelToronto General Hospital, UHN and Princess Margaret Cancer Centre, Toronto, ONT, Canada.
Peter R GalleUniversity Medical Center Mainz, I. Department of Internal Medicine, Mainz, Germany.
Masatoshi KudoDepartment of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Lorenza RimassaDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Hong Jae ChonMedical Oncology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
Giuseppe CabibboSection of Gastroenterology & Hepatology, Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, PROMISE, University of Palermo, Palermo, Italy.
Fabio PiscagliaDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Calogero CammàSection of Gastroenterology & Hepatology, Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, PROMISE, University of Palermo, Palermo, Italy.
Anjana PillaiDepartment of Internal Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Chicago, Chicago, IL, USA.
Mario PirisiDepartment of Translational Medicine, Università del Piemonte Orientale, Novara, Italy.
Amit G SingalDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
David J PinatoDepartment of Translational Medicine, Università del Piemonte Orientale, Novara, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: Atezolizumab plus bevacizumab (A+B) is a standard-of-care treatment in unresectable hepatocellular carcinoma (uHCC). Verification of its effectiveness outside clinical trials is an area of unmet need, especially in estimating long-term survival outcomes. Methods: We conducted a systematic review and meta-analysis of the MEDLINE, Embase, and Cochrane libraries to evaluate therapy outcomes in patients treated with frontline A+B for uHCC outside trials. Pooled estimates of overall survival (OS) and progression-free survival (PFS) at 6 and 12 months were calculated from individual patient-level data using random-effects analysis. Results: Of 2,179 patients selected from 12 cohorts, 80.5% were male, median age was 66 years (IQR 61.6-73.0), 61.6% had advanced-stage hepatocellular carcinoma (HCC), and 83.6% were Child-Pugh (CP) class A. Pooled 6- and 12-month OS was 82% (95% CI: 76-86%; Conclusions: The effectiveness of A+B after registration mirrors its efficacy estimates from clinical trial datasets. Long-term survival at 24 months can be achieved in up to 39% of patients with uHCC treated with A+B in routine clinical practice. Impact and implications: This study provides real-world evidence supporting the long-term efficacy of atezolizumab plus bevacizumab (A+B) for unresectable hepatocellular carcinoma, showing survival outcomes similar to those achieved in clinical trials. These findings are important for clinicians in supporting A+B as a frontline treatment, particularly for patients with Child-Pugh class A liver function. They also offer valuable insights for policymakers and researchers for optimising treatment strategies for unresectable hepatocellular carcinoma. However, results should be interpreted with caution because of potential variability in patient populations.

Indexed as

Child–PughHCCImmunotherapyRWESurvival

Identifiers

PMID40677696
PMCPMC12269603

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.