Evidence map›Paper›PMID 40810932›Full record

ArticleJAMA oncology2025

Integrating Quality of Life and Survival in Systemic Therapy for Advanced Hepatocellular Carcinoma: A Network Meta-Analysis.

Ciro Celsa, Gabriele Di Maria, Pasquale Lombardi, Antonio D'Alessio, Claudia A M Fulgenzi, Leonardo Brunetti, Giulia F Manfredi, Bernardo Stefanini, Alba Sparacino, Cristina Rigamonti and 7 more

Abstract readNetwork Meta-Analysis
In one paragraph

Article in JAMA oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

17 authors.

Ciro CelsaGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.
Gabriele Di MariaGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.
Pasquale LombardiDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Antonio D'AlessioDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Claudia A M FulgenziDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Leonardo BrunettiDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Giulia F ManfrediDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Bernardo StefaniniDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Alba SparacinoGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.
Cristina RigamontiDepartment of Translational Medicine, Università Del Piemonte Orientale, Novara, Italy.
Mario PirisiDepartment of Translational Medicine, Università Del Piemonte Orientale, Novara, Italy.
Charles LatchfordDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Marco VaccaroDepartment of Economic, Business, and Statistical Sciences, University of Palermo, Palermo, Italy.
Marco EneaGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.
Calogero CammàGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.
Giuseppe CabibboGastroenterology and Hepatology Unit, Department of Health Promotion, Mother & Child Care, Internal Medicine & Medical Specialties, University of Palermo, Palermo, Italy.
David James PinatoDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Multiple immunotherapy-based combinations and tyrosine kinase inhibitors are approved for first-line treatment of unresectable or advanced hepatocellular carcinoma (HCC). While overall survival remains the primary efficacy end point, health-related quality of life (HR-QoL) represents a crucial complementary outcome that has not been comprehensively compared across available treatments. Objective: To compare the HR-QoL effects associated with different first-line treatments for unresectable or advanced HCC and to integrate treatment-induced survival benefit with impact on patients' HR-QoL. Data Sources: The MEDLINE, CENTRAL, and Scopus databases were systematically searched for studies published from inception through November 2024. The search was supplemented with manual reviews of reference lists and abstracts from main oncology conferences from the past 5 years (2020-2024). Study Selection: Phase 3 randomized clinical trials comparing tyrosine kinase inhibitor monotherapy to immune checkpoint inhibitor-based therapies in first-line advanced HCC and reporting HR-QoL deterioration were included. Data Extraction and Synthesis: Study selection and data extraction were performed by 2 independent reviewers, following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. The Cochrane Collaboration tool was used to assess risk of bias. A bayesian network meta-analysis was performed using sorafenib as the comparator. Main Outcomes and Measures: Time to deterioration of HR-QoL domains were assessed using the European Organization for Research and Treatment of Cancer's Quality-of-Life Questionnaire Core 30 and HCC18. Treatment ranking was calculated using surface under the cumulative ranking (SUCRA) for HR-QoL items. Results: Seven HR-QoL items from 9 randomized clinical trials enrolling 6425 patients met inclusion criteria. SUCRA calculations showed that atezolizumab plus bevacizumab had the highest probability of reducing deterioration of global health status and QoL (85%), abdominal swelling (95%), jaundice (89%), and pain (86%). When integrating HR-QoL with overall survival, atezolizumab plus bevacizumab outperformed all other treatments across all items. Conclusions and Relevance: This network meta-analysis found that atezolizumab plus bevacizumab provides the best balance between QoL preservation and overall survival benefit compared to other systemic therapy options in unresectable or advanced HCC. This integrated assessment of survival and quality of life outcomes offers a more patient-centered approach for treatment selection in clinical practice.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsQuality of LifeHumansImmune Checkpoint InhibitorsProtein Kinase InhibitorsRandomized Controlled Trials as TopicImmune Checkpoint InhibitorsProtein Kinase Inhibitors

Identifiers

PMID40810932
PMCPMC12355390

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.