Evidence map›Paper›PMID 41337859›Full record

Trial reportESMO open2025

Radiomic signatures to estimate survival in patients with advanced hepatocellular carcinoma treated with sorafenib: Cancer and Leukemia Group B 80802 (Alliance).

L Dercle, S Geyer, A B Nixon, F Innocenti, Q Shi, S B Jacobson, L Luk, A Liu, H Yang, Y Wen and 10 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in ESMO open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

L DercleDepartment of Radiology, New York-Presbyterian/Columbia University Irving Medical Center, New York, USA; Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA. Electronic address: derclel@mskcc.org.
S GeyerAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, USA.
A B NixonDuke Cancer Institute, Duke University, Durham, USA.
F InnocentiDivision of Pharmacotherapy and Experimental Therapeutics, University of North Carolina, Chapel Hill, USA.
Q ShiAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, USA.
S B JacobsonAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, USA.
L LukDepartment of Radiology, New York-Presbyterian/Columbia University Irving Medical Center, New York, USA.
A LiuDepartment of Physics, NewYork-Presbyterian/Columbia University Irving Medical Center, New York, USA.
H YangDepartment of Radiology, New York-Presbyterian/Columbia University Irving Medical Center, New York, USA; Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA.
Y WenAlliance Protocol Operations Office, University of Chicago, Chicago, USA.
B ZhaoDepartment of Radiology, New York-Presbyterian/Columbia University Irving Medical Center, New York, USA; Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA.
T EcheDepartment of Radiology, New York-Presbyterian/Columbia University Irving Medical Center, New York, USA; Department of Radiology, Toulouse Rangueil Hospital, Toulouse, France.
F-Z MokraneDepartment of Radiology, Toulouse Rangueil Hospital, Toulouse, France.
M YangDepartment of Radiology, New York-Presbyterian/Columbia University Irving Medical Center, New York, USA; McGovern Medical School at University of Texas Health Science Center Houston, Houston, USA.
J MeyerhardtDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA.
E M O'ReillyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA; Department of Medicine, Weill Medical College of Cornell University, New York, USA.
A P VenookUCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, USA.
A B El-KhoueiryUSC Norris Comprehensive Cancer Center, Los Angeles, USA.
L H SchwartzDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA.
G K Abou-AlfaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
THE ALLIANCE NCTN BIOREPOSITORY AND BIOSPECIMEN RESOURCEU24CA196171 · NCI · WASHINGTON UNIVERSITY · PI Mine Cicek, Wendy Frankel · 2015 to 2026
$35.0M
Network Lead Academic Participating Site: Memorial Sloan Kettering Cancer CenterUG1CA233290 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CAROL AGHAJANIAN, Darren Feldman · 2019 to 2026
$10.2M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
UG1 - NCTN (Network Lead)UG1CA233327 · NCI · UNIVERSITY OF CHICAGO · PI STEVEN J CHMURA, HEDY L KINDLER · 2019 to 2026
$4.4M
The Duke University - Duke Cancer Institute National Clinical Trials Network LAPS (UG1) Support GrantUG1CA233253 · NCI · DUKE UNIVERSITY · PI John H Strickler, Alexandra Thomas · 2019 to 2026
$3.7M
UNC Lead Academic Participating SiteUG1CA233373 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CAREY, LISA A, DEES, ELIZABETH CLAIRE · 2019 to 2025
$3.5M
NCTN - Network Lead Academic Participating Site: USCUG1CA180830 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Anthony Boutros El-Khoueiry, Amir Goldkorn · 2019 to 2026
$3.2M
NCI NIH HHS P30 CA008748NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180882NCI NIH HHS U24 CA196171NCI NIH HHS UG1 CA180830NCI NIH HHS UG1 CA233180NCI NIH HHS UG1 CA233253NCI NIH HHS UG1 CA233290NCI NIH HHS UG1 CA233327NCI NIH HHS UG1 CA233373
6 · The paper itself

Abstract

backgroundCurrent methods to evaluate therapeutic response in patients with hepatocellular carcinoma (HCC) rely on tumor size and density, which do not always correlate well with survival. We used pretreatment clinical and radiomics variables to predict overall survival (OS) in the randomized phase III CALGB 80802 (Alliance) trial, investigating the efficacy of sorafenib + doxorubicin versus sorafenib alone. MATERIALS AND

methodsUsing machine learning, we analyzed baseline and first follow-up computed tomography (CT) images and associated clinical metadata from patients imaged in February 2010-May 2015, up to November 2015 with follow-up. Adult patients with HCC (n = 129) were randomly assigned to training (n = 92) and validation (n = 37) sets. We assessed the performance of a signature combining CT imaging features and clinical variables using hazard ratios to estimate OS after week 10 (first follow-up).

resultsMost patients were male (86.6%) and had bilirubin <2 mg/dl (98.4%), albumin >3.5 g/dl (69.0%), and moderately differentiated HCC (34.1%). Median (interquartile range) age: 58 years (63-71 years), alpha-fetoprotein (AFP): 2.5 ng/ml (26-282 ng/ml), international normalized ratio: 1 (1.1-1.2), Child-Pugh score: 5 (5-6). The highest-performing parsimonious training set signature combined clinical and radiomics features at baseline and week 10. In the validation set, the hazard ratio was 2398 (95% confidence interval 121-47 371) (P < 0.001). The signature's variables, ranked by importance, included baseline clinical features [albumin (1), AFP (2), Child-Pugh (4)], baseline radiomics features [component 17 (3), component 1 (5), component 9 (7), tumor volume (8)], and week 10 radiomics features [delta tumor volume (6)].

conclusionOS can be accurately predicted in patients with HCC receiving sorafenib by combining certain radiomics features with clinical metadata, centered primarily on baseline characteristics.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularLiver NeoplasmsSorafenibAdultAgedFemaleHumansMaleMiddle AgedRadiomicsTomography, X-Ray ComputedTreatment OutcomeAntineoplastic AgentsSorafenibclinical featureshepatocellular carcinomamachine learningoverall survivalradiomicstumor volume

Identifiers

PMID41337859
PMCPMC12720083

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Registered trials

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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.