Radiomics-based prediction of HCC response to atezolizumab/bevacizumab.

I Isaac Rodriguez (Division of Hepatology, Division of Clinical Bioinformatics, Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany) A Abhinay Vellala T Timo Itzel (Clinical Cooperation Unit Healthy Metabolism, Center for Preventive Medicine and Digital Health Baden-Württemberg (CPDBW), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany) M Michael Vácha (Division of Hepatology, Division of Clinical Bioinformatics, Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany) D De-Hua Chang M Michael Dill (Department of Gastroenterology, Hepatology, Infectious Diseases and Intoxications, Heidelberg University Hospital, Heidelberg, Germany) M Max Seidensticker J Julia Mayerle S Stefan Munker (Department of Medicine II, University Hospital, LMU Munich, Munich, Germany) S Stefan O. Schönberg (Universtitätsmedizin Mannheim, Mannheim, Germany) L Lukas Mueller P Peter Robert Galle A Arndt Weinmann D Dietmar Tamandl M Matthias Pinter B Bernhard Scheiner A Andreas Teufel (Division of Hepatology, Division of Clinical Bioinformatics, Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany) M Matthias Froelich M Matthias Philip Ebert (Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany) M Marino Venerito (Department of Gastroenterology, Hepatology & Infectious Diseases, Otto-von-Guericke University Hospital, Magdeburg, Germany)

Abstract

636 Background: Advanced hepatocellular carcinoma (HCC) treatment has evolved with the introduction of atezolizumab/bevacizumab, showing improved outcomes over sorafenib. However, the response varies among patients, particularly between viral and non-viral etiologies. This study aimed to develop and evaluate multimodal prediction models combining quantitative imaging and clinical markers to predict treatment response in HCC patients. Methods: From March 2020 to May 2023, patients with advanced HCC treated with atezolizumab/bevacizumab were retrospectively identified from six centers in Germany and Austria. Patients underwent baseline contrast-enhanced liver MRI and follow-up imaging to assess therapy response. Machine learning models, including RandomForestClassifier, were developed for radiomics, clinical, and combined datasets. Hyperparameter tuning was performed using RandomizedSearchCV, followed by cross-validation to evaluate model performance. Results: The study included 103 patients, with 70 achieving disease control (DC) and 33 experiencing disease progression (PD). Key findings included significant differences in treatment response and progression-free survival between DC and PD groups. The radiomics model, using 14 selected features, achieved 73.1% accuracy and a ROC AUC of 0.635 on the test set. The clinical model, with 4 selected features, achieved 73% accuracy and a ROC AUC of 0.649 on the test set. The combined model showed improved performance with 69% accuracy and a ROC AUC of 0.753 on the test set. Hyperparameter tuning further enhanced the combined model's accuracy to 80.1% and ROC AUC to 0.771 on the test set. Conclusions: The hybrid model combining clinical and radiological data outperformed individual models, providing better predictions of response to atezolizumab/bevacizumab in HCC patients.

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 636-636
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

I

Isaac Rodriguez

Division of Hepatology, Division of Clinical Bioinformatics, Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

A

Abhinay Vellala

T

Timo Itzel

Clinical Cooperation Unit Healthy Metabolism, Center for Preventive Medicine and Digital Health Baden-Württemberg (CPDBW), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

M

Michael Vácha

Division of Hepatology, Division of Clinical Bioinformatics, Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

D

De-Hua Chang

M

Michael Dill

Department of Gastroenterology, Hepatology, Infectious Diseases and Intoxications, Heidelberg University Hospital, Heidelberg, Germany

M

Max Seidensticker

J

Julia Mayerle

S

Stefan Munker

Department of Medicine II, University Hospital, LMU Munich, Munich, Germany

S

Stefan O. Schönberg

Universtitätsmedizin Mannheim, Mannheim, Germany

L

Lukas Mueller

P

Peter Robert Galle

A

Arndt Weinmann

D

Dietmar Tamandl

M

Matthias Pinter

B

Bernhard Scheiner

A

Andreas Teufel

Division of Hepatology, Division of Clinical Bioinformatics, Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

M

Matthias Froelich

M

Matthias Philip Ebert

Department of Medicine II, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

M

Marino Venerito

Department of Gastroenterology, Hepatology & Infectious Diseases, Otto-von-Guericke University Hospital, Magdeburg, Germany