Evidence map›Paper›PMID 42839680›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2026

Stratifying Cardiovascular Risk in Patients With HCC Receiving Atezolizumab/Bevacizumab: A Comparison of ESC and CARDIOSOR Scores.

Bernardo Stefanini, Lorenza Rimassa, Massimo Iavarone, Giuseppe Cabibbo, Fabio Marra, Caterina Vivaldi, Andrea Dalbeni, Francesca Romana Ponziani, Andrea Palloni, Sara Lonardi and 23 more

Registry-linked trialAbstract readMulticenter StudyComparative Study
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06806579 (Atezolizumab-bevacizumab and Other Immunotherapies), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT06806579 recruitingnot on this map

Atezolizumab-bevacizumab and Other Immunotherapies: Real-life Experience for Treatment of Hepatocellular Carcinoma

TypeobservationalSponsorIRCCS Azienda Ospedaliero-Universitaria di BolognaRan2022 to 2031Enrolled1,000ConditionsHepatocellular Carcinoma (HCC)
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Stratifying Cardiovascular Risk in Patients With HCC Receiving Atezolizumab/Bevacizumab: A Comparison of ESC and CARDIOSOR Scores.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
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

33 authors.

Bernardo StefaniniDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-3800-5678
Lorenza RimassaDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.ORCID https://orcid.org/0000-0001-9957-3615
Massimo IavaroneDivision of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID https://orcid.org/0000-0003-3493-6504
Giuseppe CabibboGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.ORCID https://orcid.org/0000-0002-0946-3859
Fabio MarraInternal Medicine and Liver Unit, University Hospital Careggi, University of Florence, Florence, Italy.ORCID https://orcid.org/0000-0001-8629-0878
Caterina VivaldiUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Andrea DalbeniUnit of General Medicine C, Medicine Department, University of Verona and University and Hospital Trust (AOUI) of Verona, Verona, Italy.ORCID https://orcid.org/0000-0003-0402-4176
Francesca Romana PonzianiLiver Unit, CEMAD Centro Malattie dell'Apparato Digerente, Medicina Interna e Gastroenterologia, Fondazione Policlinico Universitario Gemelli IRCCS, Rome, Italy.
Andrea PalloniMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Sara LonardiOncology Unit 1, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.ORCID https://orcid.org/0000-0002-7593-8138
Lorenzo LaniUnit of Semeiotics, Liver and Alcohol-Related Diseases, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0001-5133-5829
Piera FedericoOncology Unit, Ospedale del Mare, Napoli, Italy.ORCID https://orcid.org/0000-0002-0863-7546
Gianluca Svegliati-BaroniLiver Injury and Transplant Unit, Polytechnic University of Marche, Ancona, Italy.
Tiziana PressianiHepatopancreatobiliary Oncology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID https://orcid.org/0000-0001-6919-1536
Luca IelasiDepartment of Internal Medicine, Ospedale Degli Infermi di Faenza, Faenza, Italy.
Chiara MazzarelliHepatology and Gastroenterology Unit, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Stefania De LorenzoOncology Unit, Azienda USL Bologna, Bologna, Italy.
Rodolfo SaccoGastroenterology and Digestive Endoscopy Unit, Foggia University Hospital, Foggia, Italy.
Mariangela BruccoleriDivision of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID https://orcid.org/0000-0001-7400-4854
Ciro CelsaGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.
Alessio MastroDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Gianluca MasiUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Alessandra AuriemmaSection of Innovation Biomedicine-Oncology Area, Department of Engineering for Innovation Medicine (DIMI), University of Verona and University and Hospital Trust (AOUI) of Verona, Verona, Italy.ORCID https://orcid.org/0000-0001-7760-2542
Leonardo StellaLiver Unit, CEMAD Centro Malattie dell'Apparato Digerente, Medicina Interna e Gastroenterologia, Fondazione Policlinico Universitario Gemelli IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0002-3431-0803
Pierluigi ToniuttoHepatology and Liver Transplantation Unit, Azienda Ospedaliero Universitaria, University of Udine, Udine, Italy.ORCID https://orcid.org/0000-0002-2566-3041
Rosanna VillaniLiver Unit, Department of Medical and Surgical Sciences, University of Foggia, Foggia, Italy.ORCID https://orcid.org/0000-0001-9875-019X
Chiara DeianaMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Sara AscariDivision of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0009-0008-9317-9746
Mariarosaria MarsegliaDivision of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-5829-4537
Alessandro GranitoDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-0637-739X
Fabio PiscagliaDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0001-8264-1845
Francesco TovoliDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-8350-1155
ARTE Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsThe management of comorbidities has become increasingly relevant in unresectable hepatocellular carcinoma (uHCC) as immunotherapy prolongs survival. Atezolizumab plus bevacizumab (AB) is a standard first-line option, but bevacizumab carries a risk of cardiovascular toxicities. Data on cardiovascular risk stratification in patients with cirrhosis remain limited. Identifying patients at increased cardiovascular risk is therefore clinically important, particularly given the availability of bevacizumab-free alternatives.

methodsWe retrospectively analysed prospectively collected data from the multicenter Italian ARTE database, including patients with uHCC treated with first-line AB between June 2022 and July 2025. Traditional major adverse cardiovascular events (tMACE) were defined as acute coronary syndromes, heart failure, cerebrovascular events, or peripheral ischemia, while an extended composite (eMACE) additionally included venous thromboembolism and immune-related myocarditis. Cardiovascular risk was stratified using the European Society of Cardiology (ESC) Cardio-Oncology classification and the CARDIOSOR score. Competing-risk analyses were performed considering treatment discontinuation as a competing event.

resultsThis study included 538 patients (median age 69.8 years). During follow-up, 20 patients (3.7%) experienced tMACE, and 30 (5.6%) experienced eMACE. Patients assigned to the very high-risk category by ESC criteria and those with a high-risk CARDIOSOR score had a significantly increased risk of tMACE and eMACE. Both scores demonstrated a moderate ability to stratify cardiovascular risk (Harrell's c-index 0.68 for ESC and 0.59 for CARDIOSOR).

conclusionsCardiovascular adverse events were uncommon overall, but their incidence was not negligible in patients in high-risk subgroups. Risk scores may help identify vulnerable subgroups and support patient-tailored treatment strategies, including consideration of bevacizumab-free regimens in selected cases.

trial registrationMulticenter ARTE database (NCT06806579).

Indexed as

Antibodies, Monoclonal, HumanizedBevacizumabCarcinoma, HepatocellularCardiovascular DiseasesLiver NeoplasmsAgedAged, 80 and overFemaleHeart Disease Risk FactorsHumansItalyMaleMiddle AgedRetrospective StudiesRisk AssessmentRisk FactorsAntibodies, Monoclonal, HumanizedatezolizumabBevacizumab

Identifiers

PMID42839680
PMCPMC13643190

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Registered trials

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 OpenQuestion graph.