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Updated: Jun 24, 2025

Predictive Immune Modeling of Solid Tumors
Published on: February 25, 2020
Integration of Clinical Trial Spatial Multiomics Analysis and Virtual Clinical Trials Enables Immunotherapy Response
Shuming Zhang1, Atul Deshpande2,3,4, Babita K Verma1
1Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Abstract:
Due to the lack of treatment options, there remains a need to advance new therapeutics in hepatocellular carcinoma (HCC). The traditional approach moves from initial molecular discovery through animal models to human trials to advance novel systemic therapies that improve treatment outcomes for patients with cancer. Computational methods that simulate tumors mathematically to describe cellular and molecular interactions are emerging as promising tools to simulate the impact of therapy entirely in silico, potentially greatly accelerating delivery of new therapeutics to patients. To facilitate the design of dosing regimens and identification of potential biomarkers for immunotherapy, we developed a new computational model to track tumor progression at the organ scale while capturing the spatial heterogeneity of the tumor in HCC. This computational model of spatial quantitative systems pharmacology was designed to simulate the effects of combination immunotherapy. The model was initiated using literature-derived parameter values and fitted to the specifics of HCC. Model validation was done through comparison with spatial multiomics data from a neoadjuvant HCC clinical trial combining anti-PD1 immunotherapy and a multitargeted tyrosine kinase inhibitor cabozantinib. Validation using spatial proteomics data from imaging mass cytometry demonstrated that closer proximity between CD8 T cells and macrophages correlated with nonresponse. We also compared the model output with Visium spatial transcriptomics profiling of samples from posttreatment tumor resections in the clinical trial and from another independent study of anti-PD1 monotherapy. Spatial transcriptomics data confirmed simulation results, suggesting the importance of spatial patterns of tumor vasculature and TGFβ in tumor and immune cell interactions. Our findings demonstrate that incorporating mathematical modeling and computer simulations with high-throughput spatial multiomics data provides a novel approach for patient outcome prediction and biomarker discovery. Significance: Incorporating mathematical modeling and computer simulations with high-throughput spatial multiomics data provides an effective approach for patient outcome prediction and biomarker discovery.
Insights
Computational modeling advances hepatocellular carcinoma (HCC) treatment by simulating therapies in silico. This approach aids in predicting patient outcomes and discovering biomarkers for immunotherapy, accelerating new drug development.
Area of Science:
- Oncology
- Computational Biology
- Immunotherapy
Background:
- Hepatocellular carcinoma (HCC) lacks effective treatment options, necessitating novel therapeutic strategies.
- Traditional drug development is lengthy and costly, involving animal models and human trials.
- In silico computational modeling offers a promising avenue to accelerate the discovery and delivery of new cancer therapies.
Purpose of the Study:
- To develop a novel computational model for simulating hepatocellular carcinoma (HCC) progression and combination immunotherapy effects.
- To facilitate the design of dosing regimens and identify potential biomarkers for HCC immunotherapy.
- To capture organ-scale tumor progression and spatial heterogeneity in HCC.
Main Methods:
- Developed a spatial quantitative systems pharmacology model for HCC.
- Initiated the model with literature-derived parameters and fitted it to HCC specifics.
- Validated the model using spatial multiomics data (proteomics, transcriptomics) from HCC clinical trials combining anti-PD1 immunotherapy and cabozantinib.
Main Results:
- Model validation using imaging mass cytometry showed proximity between CD8 T cells and macrophages correlated with nonresponse.
- Spatial transcriptomics data confirmed simulation results, highlighting the role of tumor vasculature and TGFβ in immune interactions.
- The model successfully predicted patient outcomes and identified potential biomarkers.
Conclusions:
- Integrating mathematical modeling and computer simulations with spatial multiomics data offers a powerful approach for HCC research.
- This combined methodology enables effective patient outcome prediction and biomarker discovery for immunotherapy.
- The developed computational model accelerates the advancement of novel therapeutics for hepatocellular carcinoma.

