Integration of Clinical Trial Spatial Multiomics Analysis and Virtual Clinical Trials Enables Immunotherapy Response Prediction and Biomarker Discovery

Author:

Zhang Shuming1ORCID,Deshpande Atul234ORCID,Verma Babita K.1ORCID,Wang Hanwen1ORCID,Mi Haoyang1ORCID,Yuan Long25ORCID,Ho Won Jin34ORCID,Jaffee Elizabeth M.234ORCID,Zhu Qingfeng6ORCID,Anders Robert A.346ORCID,Yarchoan Mark234ORCID,Kagohara Luciane T.234ORCID,Fertig Elana J.12347ORCID,Popel Aleksander S.13ORCID

Affiliation:

1. Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland. 1

2. Bloomberg-Kimmel Immunotherapy Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, Maryland. 2

3. Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland. 3

4. Convergence Institute, Johns Hopkins University, Baltimore, Maryland. 4

5. Department of Immunology, Johns Hopkins University School of Medicine, Baltimore, Maryland. 6

6. Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland. 5

7. Department of Applied Mathematics and Statistics, Johns Hopkins University School of Medicine, Baltimore, Maryland. 7

Abstract

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.

Funder

National Cancer Institute

Johns Hopkins University

Congressionally Directed Medical Research Programs

Publisher

American Association for Cancer Research (AACR)

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